Developmental Delays and Regressions

Total Page:16

File Type:pdf, Size:1020Kb

Developmental Delays and Regressions CHALLENGING CASE: DEVELOPMENTAL DELAYS AND REGRESSIONS A Two-Year-Old Boy with Language Regression and Unusual Social Interactions* CASE his brother seems to prefer me.” The parents’ mar- Jimmy, a 21⁄2-year-old boy, was seen for the first riage was strong and free of any major disharmony. time by a new pediatrician after a recent family During the interview, the pediatrician noted that move. His mother made the appointment for a health Jimmy played persistently with his set of small supervision visit although she had concerns about trains, repetitiously lining them up in order. He was his language and social skills. She stated that he not interested in other toys that were on the floor spoke primarily with unintelligible sounds and often next to him. He ran around the trains, mostly on his communicated by pointing with his finger. He spoke toes, while making unintelligible sounds. He looked only 10 words that were clear enough to be under- away when the pediatrician called his name and stood. Jimmy’s mother said that he could hear, but became agitated when his mother attempted to redi- she was not sure whether he understood everything rect his attention to the examination. she said. Although he played at home with his The pediatrician, 4 years in practice after his resi- 4-year-old brother, he typically played by himself dency, had never seen a child with Jimmy’s pattern when he was in the presence of other children. Jim- of development. That Jimmy’s development was un- my’s mother was asked if he had had a 2-year-old usual in two domains was apparent to his pediatri- visit to a pediatrician and what the assessment was cian from the preceding information and brief obser- at that time. She said that his delayed development vations. He asked himself what the next steps should was discussed with the pediatrician, but she was be. reassured that he would progress during the follow- Index terms: language delay, developmental regression, autistic spec- ing year. trum disorder, autism, pervasive developmental delay. An uncomplicated full-term gestation was fol- lowed by a vaginal delivery without perinatal prob- Dr. Martin T. Stein lems. Jimmy was a “calm” baby who was breastfed At the end of the second year of life, Jimmy expe- for the first 6 months of life. He sat at 7 months, rienced a loss of previously acquired language skills pulled himself up to stand with support at approxi- associated with several atypical behaviors during mately 9 months, and walked at 13 months. Transi- play and social interactions. Regression of language tions were always difficult for Jimmy; he screamed skills persisted and was temporally associated with and was difficult to settle whenever cared for by periodic separations from his father because of his someone other than his parents. He typically resists father’s employment demands. Jimmy’s attention physical contact when children or adults approach was sustained when he played repetitively with him. His mother recalled that language emerged trains, which he preferred to line up in a specific early. He acquired a significant number of words order; however, he could not be engaged in either between 12 and 15 months of age. Jimmy apparently conversation or play with his pediatrician. recognized letters when his parents were teaching The monitoring and assessment of language mile- the older sibling. At 15 months, Jimmy’s language stones are, arguably, the most challenging compo- output regressed dramatically, and by 18 months, he nents of developmental surveillance for most pedia- no longer used words to communicate. Since then, he tricians. The range of predicted acquisition of many has spoken fewer than 10 single words. He mostly language skills is broad, and pediatricians often must babbles and uses repetitions of the same sounds. rely on a parent’s report rather than on clinical ob- The pediatrician inquired into family structure and servation. What makes this case different from the life events at the time Jimmy lost language mile- toddler who presents isolated language delay is the stones. He was told that, at this time, the father, an presence of unusual social skills and sensitivities. It engineer, changed his position in the company and should immediately raise the possibility of a perva- began to travel extensively. Jimmy’s mother thought sive developmental disorder (PDD) and other diag- that the absence of his father might be related to the nostic categories. language regression. She also noted that Jimmy As a result of an expanded perspective on the seemed to have a stronger attachment for his father: initial presentation, diagnostic criteria, interventions, “Jimmy has always been attracted to his father, and and prognosis of children with PDD (also known as “autistic spectrum disorder”), expectations for early * Originally published in J Dev Behav Pediatr. 2000;21(4) recognition, referral for evaluation, and treatment PEDIATRICS (ISSN 0031 4005). Copyright © 2001 by the American Acad- have changed dramatically. Ten to 15 years ago, a emy of Pediatrics and Lippincott Williams & Wilkins. general pediatrician with a busy office practice may 910 PEDIATRICS Vol.Downloaded 107 No. 4from April www.aappublications.org/news 2001 by guest on September 24, 2021 not have recognized a toddler with mild to moderate adjustment reaction that usually lasts less than 6 developmental delays consistent with an autistic months. It is now more than a year since the stressful spectrum disorder. In fact, the average age of diag- event, and the language and behavior are unusual, as nosis of PDD in the United States is 3 to 4 years. well as delayed. Currently, however, there is sufficient empirical re- Language regression with autistic behavior sug- search to demonstrate the effectiveness of early and gests the Landau-Kleffner (L-K) syndrome, epilepti- intensive interventions in optimal educational set- form aphasia. This disorder presents with loss of tings when they occur for at least 2 years during the language and seizures, often subclinical, and some- preschool period.1,2 Recent studies demonstrate im- times is only apparent on an overnight sleep electro- proved outcomes in most young children with au- encephalogram (EEG) or other special studies. Tem- tism, including speech in 75% or more and signifi- poral sharp waves are typical. Recent reports suggest cant improvement in social skills and intellectual that EEG irregularities are as common in autism as in performance.3,4 The challenge now for primary care L-K syndrome, blurring the distinction. Treatment is pediatricians is to design and implement an office- high-dose steroids for 6 to 12 weeks and analeptic based screening program that is sufficiently sensitive medications. Sustained, dramatic improvements can to identify those young children who might benefit be seen with treatment, especially in the youngest from further assessment. children.2,3 Drs. Charles Cowan and Suzanne Dixon com- Fragile X syndrome should be considered, espe- ment on a diagnostic approach to Jimmy’s presenta- cially if this boy has long ears and face and hyper- tion with the limited information available in the extensible joints. At 2 years of age, his testes would case summary. The history obtained from Jimmy’s be of normal size and the phenotype subtle. CATCH mother and the brief office observations reflect time 22, another chromosomal disorder, is also a possibil- limitations in most primary care settings. Dr. Cowan ity and can present the behavioral profile without the is a Clinical Professor of Pediatrics at the University cardiac or other features. Other considerations are of Washington. Before joining the Neurodevelop- the neurocutaneous syndromes, especially the tuber- mental Program at the Children’s Hospital and Re- ous sclerosis complex. A careful skin examination gional Medial Center in Seattle, he was a primary should be performed for depigmented macules, of- care pediatrician. He brings the perspective of a gen- ten the first visible sign of the disease and only seen eralist into the discussion. Dr. Dixon is a develop- with an ultraviolet light (Wood’s lamp). A complete mental-behavioral pediatrician and Emeritus Profes- family history is in order; family studies have shown sor of Pediatrics at the University of California San a 50- to 100-fold increase in the rate of autism in Diego. Currently she is at the Great Falls Clinic in first-degree relatives. Metabolic disorders and con- Great Falls, Montana, where she evaluates and treats genital infections may result in an autistic-like pro- children who have a wide range of developmental file, but they would usually present with a general- and behavioral problems. ized delayed pattern of early development and microcephaly. Most children with autistic disorders Martin T. Stein, MD have large head sizes compared with typically de- Professor of Pediatrics veloping children. If there have been regressions in University of California, San Diego School of other areas of development, the differential diagno- Medicine San Diego, California sis widens to include several neurodegenerative dis- orders. REFERENCES A temperamental profile of social withdrawal, poor adaptability, and high persistence could explain 1. Anderson SR, Campbell S, Cannon BO: The May Center for early some of Jimmy’s unusual behaviors. However, the childhood education, in Harris S, Handleman J (eds): Preschool Educa- tion Programs for Children with Autism. Austin, TX, Pro-Ed, 1994, pp atypical language and the restricted and repetitive 15–36 play patterns are not explained by temperamental 2. Ozonoff S, Cathcart K: Effectiveness of a home program intervention for differences alone. A severe language disorder can young children with autism. J Autism Dev Disord 28:25–32, 1998 present with some of the atypical behaviors de- 3. Dawson G, Osterling J: Early intervention in autism: Effectiveness and common elements of current approaches, in Guralnick MJ (ed): The scribed here.
Recommended publications
  • Is There a 'Regressive Phenotype' of Autism Spectrum Disorder Associated with the Measles-Mumps-Rubella Vaccine?
    Journal of Autism and Developmental Disorders, Vol. 36, No. 3, April 2006 (Ó 2006) DOI 10.1007/s10803-005-0070-1 Published Online: April 28, 2006 Is There a ‘Regressive Phenotype’ of Autism Spectrum Disorder Associated with the Measles-Mumps-Rubella Vaccine? A CPEA Study Jennifer Richler,1 Rhiannon Luyster,1 Susan Risi,1 Wan-Ling Hsu,1 Geraldine Dawson,2 Raphael Bernier,2 Michelle Dunn,3 Susan Hepburn,4 Susan L. Hyman,5 William M. McMahon,6 Julie Goudie-Nice,6 Nancy Minshew,7 Sally Rogers,8 Marian Sigman,9 M. Anne Spence,10 Wendy A. Goldberg,10 Helen Tager-Flusberg,11 Fred R. Volkmar,12 and Catherine Lord13 A multi-site study of 351 children with Autism Spectrum Disorders (ASD) and 31 typically developing children used caregiver interviews to describe the children’s early acquisition and loss of social-communication milestones. For the majority of children with ASD who had experienced a regression, pre-loss development was clearly atypical. Children who had lost skills also showed slightly poorer outcomes in verbal IQ and social reciprocity, a later mean age of onset of autistic symptoms, and more gastrointestinal symptoms than children with ASD and no regression. There was no evidence that onset of autistic symptoms or of regression was related to measles-mumps-rubella vaccination. The implications of these findings for the existence of a ‘regressive phenotype’ of ASD are discussed. KEY WORDS: Autism spectrum disorder; language development; regression; Autism Diagnostic Interview - Revised (ADI-R); measles-mumps-rubella (MMR) vaccine; gastrointestinal disorders. While most children with Autism Spectrum Dis- orders (ASD) are described as showing developmental differences from birth or early in infancy, a substantial 1 University of Michigan, Ann Arbor, USA.
    [Show full text]
  • Childhood Disintegrative Disorder (CDD): Symptomatology of the Norwegian Patient Population and Parents’ Experiences of Patient Regression
    Journal of Autism and Developmental Disorders https://doi.org/10.1007/s10803-021-05023-7 ORIGINAL PAPER Childhood Disintegrative Disorder (CDD): Symptomatology of the Norwegian Patient Population and Parents’ Experiences of Patient Regression Martin John Ellis1 · Kenneth Larsen2 · Sophie Seychelle Havighurst1,3 Accepted: 13 April 2021 © The Author(s) 2021 Abstract Childhood Disintegrative Disorder (CDD) is a rare and little researched developmental disorder characterised by regression in language and social skills after a period of seemingly normal development until at least the age of 2 years. The study contacted all parents of CDD patients in Norway to assess patient symptomatology and parents’ experiences of regression via questionnaire or interview. There were 12 participants. Symptomatology was in-line with previous studies, with universal regression in language and social skills and onset predominantly at 2–4 years. Regression was connected to feelings of ‘loss’ and uncertainty over the prognosis for CDD patients. The study supported CDD diagnostic criteria and showed that CDD patient regression has profound implications for parental well-being. Keywords CDD · Childhood Disintegrative Disorder · Heller Syndrome · Autism · Regression Childhood Disintegrative Disorder (CDD) is a rare and lit- challenging and uncertainty regarding its diagnostic charac- tle understood form of pervasive developmental disorder teristics, and even its diagnostic validity, remain. (PDD). CDD is typifed by a period of normal development CDD was frst described by Theodor Heller in 1908 and in the child for at least two years before a period of pro- termed ‘dementia infantilis’ (Mouridsen, 2003). Since this found and irreversible regression in social and cognitive time a variety of terms have been used for what, to all intents skills (Mehra et al., 2018).
    [Show full text]
  • Autism with and Without Regression: a Two-Year Prospective Longitudinal Study in Two Population-Derived Swedish Cohorts
    Journal of Autism and Developmental Disorders https://doi.org/10.1007/s10803-018-03871-4 ORIGINALPAPER Autism With and Without Regression: A Two-Year Prospective Longitudinal Study in Two Population-Derived Swedish Cohorts Lucy Thompson1,2 · Christopher Gillberg1,2 · Sara Landberg1 · Anne‑Katrin Kantzer1 · Carmela Miniscalco1 · Martina Barnevik Olsson1,3 · Mats A. Eriksson1,4 · Elisabeth Fernell1 © The Author(s) 2019 Abstract Two community-based cohorts of children with autism spectrum disorder, examined using similar assessment protocols, were pooled (n = 301) and subdivided according to history of regression. Those with regression (n = 62), 20.5% of the com- bined cohort, were contrasted with those without regression (n = 241) at first assessment (age range 19–60 months) and at 2-year follow-up on a range of measures. The regression group was significantly more functionally impaired, with regard to intellectual function (p < .001), language development (p < .001), and to severity of autism (p < .01) at both T1 and T2. Only 14 (23.3%) had a clearly identified underlying etiology [24 (18.6%) in the non-regressive group]. There were no significant differences between those who had regressed ‘from normal’ and those who had regressed ‘from low’ functioning. Keywords Autism · ASD · Regressive autism · Non-regressive autism · Intellectual developmental disorder · Developmental language disorder Introduction (i.e., rely on existing diagnoses within a population (e.g., Baird et al. 2008). The few systematic studies that have been Many children with autism spectrum disorder (ASD) published seem to indicate that regression in autism is (a) (American Psychiatric Association 2013) have shown mild not uncommon, but the relative prevalence is not known, and or marked developmental problems from early childhood (b) associated with high rated of intellectual developmental (Coleman and Gillberg 2012).
    [Show full text]
  • Regression in Rett Syndrome May Inform Autism
    Spectrum | Autism Research News https://www.spectrumnews.org VIEWPOINT Regression in Rett syndrome may inform autism BY JEFFREY NEUL 18 JUNE 2013 A. Kramer, Texas Children's HospitalDelayed onset: Jeffrey Neul studies Rett syndrome, which is characterized by a loss of language and motor ability around 1 year of age. There seem to be two broad patterns of disease progression in autism. Many individuals with the disorder show features within the first year of life, with gradually developing impairments in social and language development1, 2. However, a significant minority displays another distinct course, marked by loss of previously acquired skills around age 1 or 2, notably in language and social interaction. The prevalence of this ‘regressive' form of autism is not known, ranging from 12 to 50 percent of people with autism. (A meta-analysis published this year found the prevalence of regression in autism to be 32.1 percent3.) Part of the reason for this wide range is differences in the way these studies define regression in autism. Regression is better understood in Rett syndrome — a neurodevelopmental disorder that resembles autism — in which regression is a defining feature4. The syndrome predominantly affects girls, who appear to have normal motor, cognitive and social development until 6 months of age. These girls may show some developmental delay, but then at 1 or 2 years of age they undergo a severe developmental regression and lose the ability to speak and use their hands. Intriguingly, regression in Rett syndrome occurs at the same time as in regressive autism, and 1 / 5 Spectrum | Autism Research News https://www.spectrumnews.org includes many of the same features,suggesting a common biological process.
    [Show full text]
  • Developmental Regression in Children
    Louisiana State University LSU Digital Commons LSU Doctoral Dissertations Graduate School 6-27-2019 Developmental Regression in Children with Autism Spectrum Disorder: Associated Factors and Outcomes Jasper Abarte Estabillo Louisiana State University and Agricultural and Mechanical College, [email protected] Follow this and additional works at: https://digitalcommons.lsu.edu/gradschool_dissertations Part of the Child Psychology Commons, Clinical Psychology Commons, and the Disability Studies Commons Recommended Citation Estabillo, Jasper Abarte, "Developmental Regression in Children with Autism Spectrum Disorder: Associated Factors and Outcomes" (2019). LSU Doctoral Dissertations. 5000. https://digitalcommons.lsu.edu/gradschool_dissertations/5000 This Dissertation is brought to you for free and open access by the Graduate School at LSU Digital Commons. It has been accepted for inclusion in LSU Doctoral Dissertations by an authorized graduate school editor of LSU Digital Commons. For more information, please [email protected]. DEVELOPMENTAL REGRESSION IN CHILDREN WITH AUTISM SPECTRUM DISORDER: ASSOCIATED FACTORS AND OUTCOMES A Dissertation Submitted to the Graduate Faculty of the Louisiana State University and Agriculture and Mechanical College in partial fulfillment of the requirements for the degree of Doctor of Philosophy in The Department of Psychology by Jasper Estabillo M.A., Louisiana State University, 2017 B.A., University of California, San Diego, 2010 August 2019 Table of Contents Abstract…………………………………………………………………...………………………iii
    [Show full text]
  • Down Syndrome Disintegrative Disorder: a Clinical Regression Syndrome of Increasing Importance Mattia Rosso, MD,A Ellen Fremion, MD,B Stephanie L
    Down Syndrome Disintegrative Disorder: A Clinical Regression Syndrome of Increasing Importance Mattia Rosso, MD,a Ellen Fremion, MD,b Stephanie L. Santoro, MD,c,d Nicolas M. Oreskovic, MD, MPH,c Tanuja Chitnis, MD,a Brian G. Skotko, MD, MPP,c,d Jonathan D. Santoro, MDe,f Down syndrome disintegrative disorder (DSDD), a developmental regression abstract in children with Down syndrome (DS), is a clinical entity that is characterized by a loss of previously acquired adaptive, cognitive, and social functioning in persons with DS usually in adolescence to early adulthood. Initially reported in 1946 as “catatonic psychosis,” there has been an increasing interest among aAnn Romney Center for Neurologic Diseases, Harvard the DS community, primary care, and subspecialty providers in this clinical Medical School, Harvard University and Brigham and area over the past decade. This condition has a subacute onset and can Women’s Hospital, Boston, Massachusetts; bInternal Medicine-Pediatrics Program, Baylor College of Medicine, include symptoms of mood lability, decreased participation in activities of Houston, Texas; cDivision of Medical Genetics and daily living, new-onset insomnia, social withdrawal, autistic-like regression, Metabolism, Department of Pediatrics, Massachusetts General Hospital, Boston, Massachusetts; dDepartment of mutism, and catatonia. The acute phase is followed by a chronic phase in Pediatrics, Harvard Medical School, Harvard University, which baseline functioning may not return. No strict criteria or definitive Boston, Massachusetts; eDepartment of Neurology, Children’s Hospital Los Angeles, Los Angeles, California; and testing is currently available to diagnose DSDD, although a comprehensive fKeck School of Medicine, University of Southern California, psychosocial and medical evaluation is warranted for individuals presenting Los Angeles, California with such symptoms.
    [Show full text]
  • Regression in Autism
    ACT-NOW Fact Sheet 54 p. 1 Regression in autism Dr Avril V. Brereton What is regression? Pervasive Developmental Disorders (PDDs), also known as Autism Spectrum Disorders (ASDs), are a group of neurodevelopmental disorders that include autistic disorder, Asperger’s Disorder, PDD- not otherwise specified (PDD-NOS), childhood disintegrative disorder (CDD) and Rett’s syndrome. PDDs involve delay and disorder in the development of communication and language skills, social interaction with others and restricted and stereotyped patterns of play and behaviour. Regression in the developmental course ASDs is not new. In 1966, Lotter described developmental setback, including loss of speech in 31% of a group of children diagnosed with autism. This factsheet gives an overview of regression in ASDs based on some recent published articles but I would recommend further reading for a fuller understanding of this topic. Children with an ASD who lose skills have become known as a subgroup called “regressive autism”. Regressive autism usually refers to a child where parents report an early history of normal development for 12-24 months which is followed by a loss of previously acquired skills. Language regression is the most obvious form of regression but it can also be accompanied by more global regression involving loss of social skills and social interest. Regression research – what do we know? 1. How common is it? Published studies have reported regression in speech, use of gesture and general development in between 22% and 50% of children with ASDs. Prevalence rates vary because of differences in the definitions used in these studies. For example, some defined language regression as loss of at least five words for a period of at least 3 months whereas others defined regression as a loss of consistent use of one word used communicatively.
    [Show full text]
  • Developmental Regression in Autism Spectrum Disorders and the Broad Autism Phenotype
    Developmental Regression in Autism Spectrum Disorders and the Broad Autism Phenotype ______________________________________ A Dissertation Presented to the Faculty of the Curry School of Education University of Virginia _______________________________________ In Partial Fulfillment of the Requirements for the Degree Doctor of Philosophy _______________________________________ by Robert Haxter, M.S., Ed.S. August 2017 DEVELOPMENTAL REGRESSION Abstract This study examined the relationship between the Broad Autism Phenotype (BAP) and developmental regression in children with Autism Spectrum Disorders. A sample of 2757 children and adolescents with autism spectrum disorders was drawn from the Simons Simplex Collection, an archival database administered by the Simons Foundation Autism Research Initiative (SFARI). The Autism Diagnostic Interview – Revised (ADI-R) was utilized to capture regression status, while the Broad Autism Phenotype Questionnaire (BAPQ) collected information pertaining to parental personality attributes (i.e., aloofness, rigidity, and use of pragmatic language) associated with the BAP. Analysis of Variance demonstrated that parents of children experiencing more significant regressions have a tendency to self-report lower BAPQ ratings than parents of children experiencing either no regression or possible regression. These effects were partially attributable to fathers of other loss children, who may have exhibited a selective blind spot in evaluating their own skill deficiencies. While fathers with BAP traits appear capable
    [Show full text]
  • Developmental Regression in Children with Down Syndrome
    DEVELOPMENTAL REGRESSION IN CHILDREN WITH DOWN SYNDROME By Susana Bernad Ripoll B.A, Universidad Pontificia de Comillas, 1999 M.S. Ed., University of Kansas, 2002 Submitted to the Department of Special Education and the Faculty of the Graduate School of the University of Kansas In partial fulfillment of the requirements for the degree of Doctor of Philosophy Dissertation Committee: ____________________________ Richard L. Simpson, Ed.D. Chairperson ____________________________ Thomas M. Skrtic, Ph.D. ____________________________ Robert G. Harrington, Ph.D. ____________________________ Michael Wehmeyer, Ph.D. ____________________________ George T. Capone, M.D. Date defended: May 6, 2011 The Dissertation Committee for Susana Bernad Ripoll certifies that this is the approved version of the following dissertation: DEVELOPMENTAL REGRESSION IN CHILDREN WITH DOWN SYNDROME Dissertation Committee: ____________________________ Richard L. Simpson, Ed.D. Chairperson ____________________________ Thomas M. Skrtic, Ph.D. ____________________________ Robert G. Harrington, Ph.D. ____________________________ Michael Wehmeyer, Ph.D. ____________________________ George T. Capone, M.D. Date approved: May 6, 2011 ABSTRACT This study presents in detail the data on a group of 20 participants, female and male, from 2 to 12 years old with Down syndrome (DS) who experienced developmental regression. This study took place at the Down syndrome clinic at Kennedy Krieger Institute, Baltimore, Maryland. These 20 participants were divided into 4 groups according to their age at regression, comorbid condition, and the characteristics of their regression. Using retrospective chart review, data showed that all 20 children lost communication, social skills, and play skills. Ten children lost some daily living skills, 8 participants had apparent motor skill changes, and 12 developed sleep disturbances.
    [Show full text]
  • Autism Spectrum Disorder-A Paediatric Dentist's Perspective
    :O p e sm n A ti c u c A e s s Autism - Open Access Berman, Autism Open Access 2015, 6:1 DOI: 10.4172/2165-7890.1000158 ISSN: 2165-7890 Perspective Article Open Access Journal Autism Spectrum Disorder-A Paediatric Dentist’s Perspective Marvin H Berman* Bridle Lane, Bannockburn, Illinois 60015, USA *Corresponding author: Berman MH, 1 Bridle Lane, Bannockburn, Illinois 60015, USA, Tel: (847)295-9393; E-mail: [email protected] Rec date: September 02, 2015; Acc date: December 14, 2015; Pub date: December 21, 2015 Copyright: © 2015 Berman MH. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Introduction the lack of babbling or meaningful gesturing, repetitive hand flapping, failure to respond to their name, excessive single word usage without Most recent reports published by the Autism and Developmental spontaneous phrases, an aversion to hugging or touching, and Disabilities Monitoring network under the auspices of the Centres for difficulty in making eye contact. All of these symptoms and others may Disease Control and Prevention predict that one in every 150 children be mild, or severe enough for parents to seek professional advice, will suffer from some kind of autistic spectrum disorder (ASD), with a hoping for a remedy [8,9]. 4-to-one prevalence of boys over girls [1]. The etiology of ASD is currently unknown, and there is no known cure [2]. In a 2009 study The American Academy of Pediatrics recommends a well-child involving phone conversations with 78,000 parents of US children who screening for ASD at 18 to 24 months of age using formal autism were identified by a health professional as having an ASD, the screening tests [10].
    [Show full text]
  • The Role of Epilepsy and Epileptiform Eegs in Autism Spectrum Disorders
    0031-3998/09/6506-0599 Vol. 65, No. 6, 2009 PEDIATRIC RESEARCH Printed in U.S.A. The Role of Epilepsy and Epileptiform EEGs in Autism Spectrum Disorders SARAH J. SPENCE AND MARK T. SCHNEIDER Pediatrics and Developmental Neuroscience Branch, National Institute of Mental Health, NIH, Bethesda, Maryland 20892-1255 ABSTRACT: Autism is a neurodevelopmental disorder of unknown occur in 1/3 of individuals with ASD. However, the exact etiology characterized by social and communication deficits and the prevalence remains unknown and the literature presents a presence of restricted interests/repetitive behaviors. Higher rates of wide range of estimates from 5 (5) to 46% (6). ASD is also epilepsy have long been reported, but prevalence estimates vary from increased in epilepsy populations, with as high as 32% (7) as little as 5% to as much as 46%. This variation is probably the result meeting diagnostic criteria. of sample characteristics that increase epilepsy risk such as sample ascertainment, lower intelligence quotient (IQ), the inclusion of There is no primary seizure type or syndrome associated patients with nonidiopathic autism, age, and gender. However, crit- with autism. Complex partial (with or without secondarily ical review of the literature reveals that the rate in idiopathic cases generalized seizures), absence, and generalized tonic-clonic with normal IQ is still significantly above the population risk sug- have all been reported (8–12). The diagnosis of seizure gesting that autism itself is associated with an increased risk of activity in autistic individuals is made more difficult because epilepsy. Recently, there has been interest in the occurrence of epilep- the behavioral abnormalities associated with complex partial tiform electroencephalograms (EEGs) even in the absence of epilepsy.
    [Show full text]
  • Landau Kleffner Syndrome, Electrical Status Epilepticus in Sleep and Autistic Regression
    Düşünen Adam Psikiyatri ve Nörolojik Bilimler Dergisi 2012;25:157-169 Derlemeler / Reviews DOI: 10.5350/DAJPN2012250209 Landau Kleffner Syndrome, Özalp Ekinci1, Uğur Işık2, İsmet Melek3 Electrical Status Epilepticus in 1Child and Adolescent Psychiatrist, Antakya Obstetrics and Child Care Hospital, Child Psyhiatry Clinic, Hatay - Turkey Sleep and Autistic Regression: 2Assist. Prof. Dr., Acıbadem University, Faculty of Medicine, Pediatric Neurology, İstanbul -Turkey, 3Assoc. Prof. Dr., Mustafa Kemal University, Faculty of An Overview of Literature Medicine, Department of Neurology, Hatay - Turkey ABSTRACT Landau kleffner syndrome, electrical status epilepticus in sleep and autistic regression: an overview of literature Language regression in children is a challenging condition for clinicians since the diagnostic and therapeutic algorithms are not well established. Landau Kleffner syndrome (LKS), Electrical Status Epilepticus in Sleep (ESES) and Autistic Regression (AR) are three rare clinical entities in which langauage regression is present. LKS and ESES appear to be two points on the spectrum of epileptic syndromes characterized by severe paroxysmal EEG disturbance in sleep and regression. However, the available literature indicates that AR has many distinct features than LKS and ESES. For all of these three conditions, early recognition and treatment is crucial for favorable outcomes. Overnight EEG has an important diagnostic role for LKS and ESES. In this review, the clinical features, prognosis and treatment options of LKS, ESES and AR will be discussed. Key words: Landau Kleffner syndrome, electrical status epilepticus in sleep, autistic regression, language regression ÖZET Landau kleffner sendromu, uykuda elektriksel status epileptikus ve otistik regresyon: Literatüre bir bakış Yazışma adresi / Address reprint requests to: Çocuklarda dil regresyonu, tanı ve tedavi yaklaşımları ile ilgili yeterli düzeyde araştırma yapılmamış olması Child and Adolescent Psychiatrist Özalp Ekinci, nedeniyle, klinisyenler için zorlayıcı bir durumdur.
    [Show full text]