Developmental Verbal Dyspraxia
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Phonological Processing Deficits As a Universal Model for Dyslexia
DOI: 10.1590/2317-1782/20142014135 Systematic Review Phonological processing deficits as a universal model Revisão Sistemática for dyslexia: evidence from different orthographies Ana Luiza Gomes Pinto Navas1 Déficit em processamento fonológico como um modelo universal Érica de Cássia Ferraz2 Juliana Postigo Amorina Borges2 para a dislexia: evidência a partir de diferentes ortografias Keywords ABSTRACT Dyslexia Purpose: To verify the universal nature of the phonological processing deficit hypothesis for dyslexia, since Education the most influential studies on the topic were conducted in children or adults speakers of English. Research Language strategy: A systematic review was designed, conducted and analyzed using PubMed, Science Direct, and Reading SciELO databases. Selection criteria: The literature search was conducted using the terms “phonological Review processing” AND “dyslexia” in publications of the last ten years (2004–2014). Data analysis: Following screening of (a) titles and abstracts and (b) full papers, 187 articles were identified as meeting the pre- established inclusion criteria. Results: The phonological processing deficit hypothesis was explored in studies involving several languages. More importantly, we identify studies in all types of writing systems such as ideographic, syllabic and logographic, as well as alphabetic orthography, with different levels of orthography- phonology consistency. Conclusion: The phonological processing hypothesis was considered as a valid explanation to dyslexia, in a wide variety of spoken languages and writing systems. Descritores RESUMO Dislexia Objetivo: Verificar a natureza universal da hipótese do déficit de processamento fonológico para a dislexia, uma Educação vez que os estudos mais influentes sobre o tema foram conduzidos com crianças ou adultos falantes do Inglês. Linguagem Estratégia de pesquisa: Uma revisão sistemática foi planejada, conduzida e analisada utilizando as bases de Leitura dados PubMed, Science Direct e SciELO. -
Foreign Accent Syndrome, a Rare Presentation of Schizophrenia in a 34-Year-Old African American Female: a Case Report and Literature Review
Hindawi Publishing Corporation Case Reports in Psychiatry Volume 2016, Article ID 8073572, 5 pages http://dx.doi.org/10.1155/2016/8073572 Case Report Foreign Accent Syndrome, a Rare Presentation of Schizophrenia in a 34-Year-Old African American Female: A Case Report and Literature Review Kenneth Asogwa,1 Carolina Nisenoff,1 and Jerome Okudo2 1 Richmond University Medical Center, 355 Bard Avenue, Staten Island, NY 10310, USA 2University of Texas School of Public Health, 1200 Pressler Street, Houston, TX 77030, USA Correspondence should be addressed to Jerome Okudo; [email protected] Received 17 October 2015; Revised 14 December 2015; Accepted 29 December 2015 AcademicEditor:ErikJonsson¨ Copyright © 2016 Kenneth Asogwa et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Foreign Accent Syndrome (FAS) is a rare phenomenon where speech is characterized by a new accent to the patient’snative language. More than 100 cases with the syndrome have been published, the majority of which were associated with observed insults of the speech center. Some other cases have been described without identifiable organic brain injury, especially in patients with psychiatric illness. This paper presents a patient with schizophrenia and FAS, without any evidence of organic brain injury. FAS recurred during psychotic exacerbation and did not reverse before transfer to a long-term psychiatric facility. The case is discussed in the context of a brief review of the syndrome. 1. Introduction had a history of paranoid schizophrenia. The patient was brought to the psychiatry emergency room by ambulance Foreign Accent Syndrome (FAS) is a rare condition where for evaluation of aggression. -
Foreign Accent Syndrome in a Patient with Multiple Sclerosis
CASE REPORT Foreign Accent Syndrome in a Patient with Multiple Sclerosis Jacqueline I Bakker, Suzanne Apeldoorn, Luanne M Metz ABSTRACT: Background: Foreign accent syndrome is a speech disorder which leads listeners to perceive the patient as having a foreign accent. It has been recognized previously after stroke, brain injury or unknown causes. Case report:A 52-year-old woman with clinically definite relapsing remitting multiple sclerosis (MS) presented with episodes of what was perceived as a Dutch accent along with other neurologic symptoms that would resolve simultaneously. She was assessed by a speech therapist both during an episode and after complete recovery. Speech and MRI changes (showing deep white matter lesions in the corpus callosum, left pariental lobe and left frontal lobe) were consistent with previous reports of foreign accent syndrome. Conclusions: This patient’s episodes of foreign accent are thought to be due to her MS. This is the first case reported of a patient with foreign accent syndrome secondary to MS. RÉSUMÉ: Syndrome de “l’accent étranger” chez une patiente atteinte de sclérose en plaques. Introduction: Le syndrome de l’accent étranger est un trouble du langage dans lequel le patient est perçu par l’entourage comme ayant un accent étranger. Cet état a déjà été observé après un accident vasculaire cérébral, un traumatisme cérébral ou sans cause connue. Observation: Une femme âgée de 52 ans, atteinte de la forme rémittente de sclérose en plaques (SEP) confirmée, a consulté pour un phénomène épisodique comprenant un trouble du langage, perçu par l’entourage comme un accent hollandais associé à d’autres symptômes neurologiques qui disparaissaient simultanément. -
A Sub-Acute Case of Resolving Acquired Apraxia of Speech and Aphasia Shannon C
hysical M f P ed l o ic a in n r e u & o R J International Journal of Physical l e a h n a o b i Mauszycki et al., Int J Phys Med Rehabil 2014, 2:2 t i l a ISSN: 2329-9096i t a n r t i e o t n 10.4172/2329-9096.1000188 n I Medicine & Rehabilitation DOI: Research Article Open Access A Sub-Acute Case of Resolving Acquired Apraxia of Speech and Aphasia Shannon C. Mauszycki1,2*, Sandra Wright1 and Julie L. Wambaugh1,2 ¹VA Salt Lake City Healthcare System, Salt Lake City, UT, USA ²University of Utah, Salt Lake City, UT, USA *Corresponding author: Shannon C. Mauszycki, Aphasia/Apraxia Research Lab, 151-A, Building 2, 500 Foothill Drive, Salt Lake City, UT 84148, USA, Tel: 801-582-1565, Ext: 2182; Fax: 801-584-5621; E-mail: [email protected] Rec date: 20 Feb 2014; Acc date:21 March 2014; Pub date: 23 March 2014 Copyright: © 2014 Mauszycki SC, et al. 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. Abstract Apraxia of speech (AOS) is a neurogenic, motor speech disorder that disrupts the planning for speech production. However, there are only a few reports that have described the evolution of stroke-induced AOS symptoms in the acute or sub-acute phase of recovery. The purpose of this report was to provide a data-based description of an individual with sub-acute AOS and aphasia followed from 1 month post-onset a stroke to 8 months post-stroke. -
The Interpretation Ofdysprosody in Patients with Parkinson's Disease 147 J Neurol Neurosurg Psychiatry: First Published As 10.1136/Jnnp.54.2.145 on 1 February 1991
Journal ofNeurology, Neurosurgery, and Psychiatry 1991;54:145-148 145 The interpretation of dysprosody in patients with J Neurol Neurosurg Psychiatry: first published as 10.1136/jnnp.54.2.145 on 1 February 1991. Downloaded from Parkinson's disease J F V Caekebeke, A Jennekens-Schinkel, M E van der Linden, 0 J S Buruma, R A C Roos Abstract functions4 has not been resolved. It would Prosodic features in the speech pro- even have implications for a revision of duction of 21 patients with idiopathic current theories on the relation between Parkinson's disease were tested. The cerebral dysfunction and disorders of emotion appreciation of vocal and facial expres- or affect. The right and left cerebral hemi- sion was also examined in the same spheres have both been suggested as the patients. Significant intergroup differ- representational locus of prosody,9 with an ences were found in the prosody produc- intrahemispheric distribution of dysprosodia tion tasks but, in contrast to previous subtypes reflecting the aphasias.'0 results, not in the receptive tasks on the The aims of the study were: (a) to verify recognition and appreciation of prosody dysprosody in a controlled replication study and of facial expression. The discrepancy of patients with PD; (b) to explore relations between the production and recognition between dysprosody and cognitive, affective of prosodic features does not support the and perceptual variables in the same patients. suggestion that dysprosody in Parkin- son's disease is necessarily a disorder of' processing emotional information that Subjects and methods could be misinterpreted as a dysarthria. Subjects Twenty one PD patients attending the outpatients clinic and 14 control subjects This study concerns "dysprosody" and its participated after giving informed consent. -
Comparison of Childhood Apraxia of Speech, Dysarthria and Severe Phonological Disorder (Some Or All of These Characteristics May Be Present
Comparison of Childhood Apraxia of Speech, Dysarthria and Severe Phonological Disorder (Some or all of these characteristics may be present. Consult with a Speech-Language Pathologist who is experienced in the diagnosis of motor speech disorders for a definitive differential diagnosis) Verbal Apraxia Dysarthria Severe Phonological Disorder No weakness, incoordination or Decreased strength and coordination No weakness, incoordination or paralysis of speech musculature of speech musculature that leads to paralysis of speech musculature imprecise speech production, slurring and distortions No difficulty with involuntary Difficulty with involuntary motor No difficulty with involuntary motor motor control for chewing, control for chewing, swallowing, control for chewing and swallowing swallowing, etc. unless there is etc. due to muscle weakness and also an oral apraxia incoordination Inconsistencies in articulation Articulation may be noticeably Consistent errors that can usually be performance--the same word may “different” due to imprecision, but grouped into categories (fronting, be produced several different errors generally consistent stopping, etc.) ways Errors include substitutions, Errors are generally distortions Errors may include substitutions, omissions, additions and omissions, distortions, etc. Omissions repetitions, frequently includes in final position more likely than initial simplification of word forms. position. Vowel distortions not as Tendency for omissions in initial common. position. Tendency to centralize vowels to -
Relevance of Aerodynamic Evaluation in Parkinsonian Dysarthria Mamadou Moustapha Sarr, Alain Ghio, Robert Espesser, Bernard Teston, Moustapha Drame, François Viallet
Relevance of Aerodynamic Evaluation in Parkinsonian Dysarthria Mamadou Moustapha Sarr, Alain Ghio, Robert Espesser, Bernard Teston, Moustapha Drame, François Viallet To cite this version: Mamadou Moustapha Sarr, Alain Ghio, Robert Espesser, Bernard Teston, Moustapha Drame, et al.. Relevance of Aerodynamic Evaluation in Parkinsonian Dysarthria. Dushanova. Diagnostics and Rehabilitation of Parkinson’s Disease, InTech, pp.207-224, 2011, 978-953-307-791-8. hal-01482597 HAL Id: hal-01482597 https://hal.archives-ouvertes.fr/hal-01482597 Submitted on 20 Apr 2018 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. 10 Relevance of Aerodynamic Evaluation in Parkinsonian Dysarthria Sarr Mamadou Moustapha1, Ghio Alain2, Espesser Robert2, Teston Bernard2, Dramé Moustapha3 and Viallet François2,4 1UFR Santé- Université deThiès 2Laboratoire Parole et Langage-Aix-en-Provence 3Université de Reims 4Service de Neurologie du Centre Hospitalier du Pays d’Aix- Aix-en-Provence 1Sénégal 2,3,4France 1. Introduction Parkinsonian dysarthria is generally known under the name of hypokinetic dysarthria. Dysarthria, according to Darley et al (1969), is characterized by all speech disorders related to disturbances of muscular control of the speech organs, whose origin is a central or peripheral nervous system injury. -
Specific Language Impairment As Systemic Developmental Disorders Christophe Parisse, Christelle Maillart
Specific language impairment as systemic developmental disorders Christophe Parisse, Christelle Maillart To cite this version: Christophe Parisse, Christelle Maillart. Specific language impairment as systemic developmental dis- orders. Journal of Neurolinguistics, Elsevier, 2009, 22, pp.109-122. 10.1016/j.jneuroling.2008.07.004. halshs-00353028 HAL Id: halshs-00353028 https://halshs.archives-ouvertes.fr/halshs-00353028 Submitted on 14 Jan 2009 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. Specific language impairment as systemic developmental disorders Christophe Parisse1 and Christelle Maillart2 1- INSERM-MoDyCo, CNRS, Paris X Nanterre University 2- University of Liège 1 Abstract Specific Language Impairment (SLI) is a disorder characterised by slow, abnormal language development. Most children with this disorder do not present any other cognitive or neurological deficits. There are many different pathological developmental profiles and switches from one profile to another often occur. An alternative would be to consider SLI as a generic name covering three developmental language disorders: developmental verbal dyspraxia, linguistic dysphasia, and pragmatic language impairment. The underlying cause of SLI is unknown and the numerous studies on the subject suggest that there is no single cause. We suggest that SLI is the result of an abnormal development of the language system, occurring when more than one part of the system fails, thus blocking the system’s natural compensation mechanisms. -
How to Find a Speech-Language Pathologist When Your Child Has Apraxia of Speech
How to Find a Speech‐Language Pathologist When Your Child Has Apraxia of Speech Your child has been diagnosed with Childhood Apraxia of Speech (CAS) or is suspected of having CAS. According to the American Speech Language Hearing Association (ASHA) Position State‐ ment ) on CAS, a speech‐language pathologist (SLP) is the appro‐ priate professional to make the diagnosis of CAS and to provide treatment for this disorder. You are now on a mission to find an SLP to treat your child. Many parents wonder: How do I begin this part of the CAS journey? This brochure is intended to provide guidance in selecting an SLP. Please note that if you live outside of the United States, your therapist may have a professional title other than SLP. What Qualifications Should I Look For in an SLP? The SLP should be certified by the American Speech Language and Hearing Association (ASHA). In order to be certified, an SLP must have completed all coursework in an accredited program, have passed a national exam, and have completed a residency called a Clinical Fellowship Year (CFY). In addition, an SLP is required to participate in continuing education in order to retain the Certificate of Clinical Competence (CCC). Look for these credentials after an SLP’s name: CCC‐SLP or CFY‐SLP (an SLP currently in his/her residency). For countries other than the United States, look for clinicians who are associate members of ASHA and/or individuals who are affiliated with the professional or‐ ganization of their country. Be aware that there are different training requirements among countries. -
Abadie's Sign Abadie's Sign Is the Absence Or Diminution of Pain Sensation When Exerting Deep Pressure on the Achilles Tendo
A.qxd 9/29/05 04:02 PM Page 1 A Abadie’s Sign Abadie’s sign is the absence or diminution of pain sensation when exerting deep pressure on the Achilles tendon by squeezing. This is a frequent finding in the tabes dorsalis variant of neurosyphilis (i.e., with dorsal column disease). Cross References Argyll Robertson pupil Abdominal Paradox - see PARADOXICAL BREATHING Abdominal Reflexes Both superficial and deep abdominal reflexes are described, of which the superficial (cutaneous) reflexes are the more commonly tested in clinical practice. A wooden stick or pin is used to scratch the abdomi- nal wall, from the flank to the midline, parallel to the line of the der- matomal strips, in upper (supraumbilical), middle (umbilical), and lower (infraumbilical) areas. The maneuver is best performed at the end of expiration when the abdominal muscles are relaxed, since the reflexes may be lost with muscle tensing; to avoid this, patients should lie supine with their arms by their sides. Superficial abdominal reflexes are lost in a number of circum- stances: normal old age obesity after abdominal surgery after multiple pregnancies in acute abdominal disorders (Rosenbach’s sign). However, absence of all superficial abdominal reflexes may be of localizing value for corticospinal pathway damage (upper motor neu- rone lesions) above T6. Lesions at or below T10 lead to selective loss of the lower reflexes with the upper and middle reflexes intact, in which case Beevor’s sign may also be present. All abdominal reflexes are preserved with lesions below T12. Abdominal reflexes are said to be lost early in multiple sclerosis, but late in motor neurone disease, an observation of possible clinical use, particularly when differentiating the primary lateral sclerosis vari- ant of motor neurone disease from multiple sclerosis. -
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Advances in Social Science, Education and Humanities Research, volume 535 Proceedings of the 1st Paris Van Java International Seminar on Health, Economics, Social Science and Humanities (PVJ-ISHESSH 2020) Analysis of the Language Delay Development in Early Children (Case Study in Bojongsoang Village, Bandung District) 1st Mulyanti Aisyiyah Bandung School of Health Sciences Bandung, Indonesia [email protected] Abstract—Language development is significant language have multiple intelligences according to their genetic and speech skills are indicators of all children's development. potential (Kemenkes RI, 2015). Speech delay (speech delay) in early childhood is when the Having children with optimal growth and development level of speech development is below the level of quality of is every parent's dream. To make it happen, of course speech development of children of the same age that can parents must always pay attention, supervise, and care for knowing from the accuracy of the use of words. A child will children carefully. The process of growth and development not be able to talk without the support of his environment. The purpose of this study was to determine the factors that in children or toddlers can take place naturally, but the influence the occurrence of language development delays and process is also very dependent on parenting from adults or the role of parents in early childhood. This research uses a parents. The toddler period is an important period in child qualitative method with a case study approach. The unit of development. Because at that time the initial or basic analysis is language development delay. There were six growth will affect and determine the child's development in speakers in this study consisting of four primary speakers. -
HIE and Speech Delays/Language Disorders
HIE and Speech Delays/Language Disorders Jump To: Speech delays and language disorders associated with HIE When should a child get speech-language therapy? What causes speech delays and language disorders? Therapy for speech delays and language disorders What happens during speech language therapy? Additional benefits of speech-language therapy Why is speech-language therapy important? About HIE Help Center Brain injury due to hypoxic-ischemic encephalopathy (HIE) is rarely confined to a single area of the brain. Because oxygen deprivation affects the connections in the brain on a global level, it is often possible that children with HIE will have multiple interrelated delays in development. Children with HIE can sometimes have delays in developing speech and language. These delays can sometimes be mitigated, while in other more severe circumstances, children may remain non-verbal and require the use of alternative or augmentative communication (AAC) technologies to potentially assist them in communicating their thoughts, needs, and desires. HIE and Speech Delays/Language Disorders | 1 HIE and Speech Delays/Language Disorders Developing a method for communicating helps these children interact with others, develop relationships, learn, work, and socialize. Speech and language are clearly highly interrelated, but they are not interchangeable (1). Speech refers to the physical act of expressing words and sounds, and encompasses the act of the muscles in the lips, tongue, vocal tract, and jaw that make recognizable sounds. Language, on the other hand, refers to communicating in a systematic and meaningful way. Because language is related to intelligence, disorders in language acquisition and expression are generally considered more serious than speech disorders.