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Journal of the National Black Association for Speech-Language and Hearing
Journal of the National Black Association for Speech-Language and Hearing Volume 13, Number 1 Spring 2018 Journal of the National Black Association for Speech-Language and Hearing Volume 13, Number 1 Spring 2018 Table of Contents To navigate through this document, use the scroll bar in the right-hand column and observe the page indicator at the bottom of the screen. Cover Page ................................................................................................................................................... 1 Table of Contents ........................................................................................................................................ 2 About the Editors ........................................................................................................................................ 4 About the Journal ....................................................................................................................................... 5 Guidelines to Authors ................................................................................................................................. 5 Manuscript Submissions ............................................................................................................................ 6 Copyrights and Permissions ...................................................................................................................... 7 Sponsoring Organization .......................................................................................................................... -
The Primary Care Pediatrician and the Care of Children with Cleft Lip And/Or Cleft Palate Charlotte W
CLINICAL REPORT Guidance for the Clinician in Rendering Pediatric Care The Primary Care Pediatrician Charlotte W. Lewis, MD, MPH, FAAP, a Lisa S. Jacob, DDS, MS, b Christoph U. andLehmann, MD, the FAAP, FACMI, Care c SECTION ON ORALof HEALTH Children With Cleft Lip and/or Cleft Palate Orofacial clefts, specifically cleft lip and/or cleft palate (CL/P), are among the abstract most common congenital anomalies. CL/P vary in their location and severity and comprise 3 overarching groups: cleft lip (CL), cleft lip with cleft palate (CLP), and cleft palate alone (CP). CL/P may be associated with one of many syndromes that could further complicate a child’s needs. Care of patients aDivision of General Pediatrics and Hospital Medicine, Department of with CL/P spans prenatal diagnosis into adulthood. The appropriate timing Pediatrics, University of Washington School of Medicine and Seattle Children’s Hospital, Seattle, Washington; bGeorgetown Pediatric and order of specific cleft-related care are important factors for optimizing Dentistry and Orthodontics, Georgetown, Texas; and Departments of cBiomedical Informatics and Pediatrics, Vanderbilt University Medical outcomes; however, care should be individualized to meet the specific needs Center, Nashville, Tennessee of each patient and family. Children with CL/P should receive their specialty All three authors participated extensively in developing, researching, cleft-related care from a multidisciplinary cleft or craniofacial team with and writing the manuscript and revising it based on reviewers’ comments; Dr Lehmann made additional revisions after review by the sufficient patient and surgical volume to promote successful outcomes. board of directors. The primary care pediatrician at the child’s medical home has an essential This document is copyrighted and is property of the American role in making a timely diagnosis and referral; providing ongoing health Academy of Pediatrics and its Board of Directors. -
Soonerstart Automatic Qualifying Syndromes and Conditions 001
SoonerStart Automatic Qualifying Syndromes and Conditions 001 Abetalipoproteinemia 272.5 002 Acanthocytosis (see Abetalipoproteinemia) 272.5 003 Accutane, Fetal Effects of (see Fetal Retinoid Syndrome) 760.79 004 Acidemia, 2-Oxoglutaric 276.2 005 Acidemia, Glutaric I 277.8 006 Acidemia, Isovaleric 277.8 007 Acidemia, Methylmalonic 277.8 008 Acidemia, Propionic 277.8 009 Aciduria, 3-Methylglutaconic Type II 277.8 010 Aciduria, Argininosuccinic 270.6 011 Acoustic-Cervico-Oculo Syndrome (see Cervico-Oculo-Acoustic Syndrome) 759.89 012 Acrocephalopolysyndactyly Type II 759.89 013 Acrocephalosyndactyly Type I 755.55 014 Acrodysostosis 759.89 015 Acrofacial Dysostosis, Nager Type 756.0 016 Adams-Oliver Syndrome (see Limb and Scalp Defects, Adams-Oliver Type) 759.89 017 Adrenoleukodystrophy, Neonatal (see Cerebro-Hepato-Renal Syndrome) 759.89 018 Aglossia Congenita (see Hypoglossia-Hypodactylia) 759.89 019 Albinism, Ocular (includes Autosomal Recessive Type) 759.89 020 Albinism, Oculocutaneous, Brown Type (Type IV) 759.89 021 Albinism, Oculocutaneous, Tyrosinase Negative (Type IA) 759.89 022 Albinism, Oculocutaneous, Tyrosinase Positive (Type II) 759.89 023 Albinism, Oculocutaneous, Yellow Mutant (Type IB) 759.89 024 Albinism-Black Locks-Deafness 759.89 025 Albright Hereditary Osteodystrophy (see Parathyroid Hormone Resistance) 759.89 026 Alexander Disease 759.89 027 Alopecia - Mental Retardation 759.89 028 Alpers Disease 759.89 029 Alpha 1,4 - Glucosidase Deficiency (see Glycogenosis, Type IIA) 271.0 030 Alpha-L-Fucosidase Deficiency (see Fucosidosis) -
Neonatal Orthopaedics
NEONATAL ORTHOPAEDICS NEONATAL ORTHOPAEDICS Second Edition N De Mazumder MBBS MS Ex-Professor and Head Department of Orthopaedics Ramakrishna Mission Seva Pratishthan Vivekananda Institute of Medical Sciences Kolkata, West Bengal, India Visiting Surgeon Department of Orthopaedics Chittaranjan Sishu Sadan Kolkata, West Bengal, India Ex-President West Bengal Orthopaedic Association (A Chapter of Indian Orthopaedic Association) Kolkata, West Bengal, India Consultant Orthopaedic Surgeon Park Children’s Centre Kolkata, West Bengal, India Foreword AK Das ® JAYPEE BROTHERS MEDICAL PUBLISHERS (P) LTD. New Delhi • London • Philadelphia • Panama (021)66485438 66485457 www.ketabpezeshki.com ® Jaypee Brothers Medical Publishers (P) Ltd. Headquarters Jaypee Brothers Medical Publishers (P) Ltd. 4838/24, Ansari Road, Daryaganj New Delhi 110 002, India Phone: +91-11-43574357 Fax: +91-11-43574314 Email: [email protected] Overseas Offices J.P. Medical Ltd. Jaypee-Highlights Medical Publishers Inc. Jaypee Brothers Medical Publishers Ltd. 83, Victoria Street, London City of Knowledge, Bld. 237, Clayton The Bourse SW1H 0HW (UK) Panama City, Panama 111, South Independence Mall East Phone: +44-2031708910 Phone: +507-301-0496 Suite 835, Philadelphia, PA 19106, USA Fax: +02-03-0086180 Fax: +507-301-0499 Phone: +267-519-9789 Email: [email protected] Email: [email protected] Email: [email protected] Jaypee Brothers Medical Publishers (P) Ltd. Jaypee Brothers Medical Publishers (P) Ltd. 17/1-B, Babar Road, Block-B, Shaymali Shorakhute, Kathmandu Mohammadpur, Dhaka-1207 Nepal Bangladesh Phone: +00977-9841528578 Mobile: +08801912003485 Email: [email protected] Email: [email protected] Website: www.jaypeebrothers.com Website: www.jaypeedigital.com © 2013, Jaypee Brothers Medical Publishers All rights reserved. No part of this book may be reproduced in any form or by any means without the prior permission of the publisher. -
Genetic Causes.Pdf
1 September 2015 Genetic causes of childhood apraxia of speech: Case‐based introduction to DNA, inheritance, and clinical management Beate Peter, Ph.D., CCC‐SLP Assistant Professor Dpt. of Speech & Hearing Science Arizona State University Adjunct Assistant Professor AG Dpt. of Communication Sciences & Disorders ATAGCT Saint Louis University T TAGCT Affiliate Assistant Professor Dpt. of Speech & Hearing Sciences University of Washington 1 Disclosure Statement Disclosure Statement Dr. Peter is co‐editor of a textbook on speech development and disorders (B. Peter & A. MacLeod, Eds., 2013), for which she may receive royalty payments. If she shares information about her ongoing research study, this may result in referrals of potential research participants. She has no financial interest or related personal interest of bias in any organization whose products or services are described, reviewed, evaluated or compared in the presentation. 2 Agenda Topic Concepts Why we should care about genetics. Case 1: A sporadic case of CAS who is missing a • Cell, nucleus, chromosomes, genes gene. Introduction to the language of genetics • From genes to proteins • CAS can result when a piece of DNA is deleted or duplicated Case 2: A multigenerational family with CAS • How the FOXP2 gene was discovered and why research in genetics of speech and language disorders is challenging • Pathways from genes to proteins to brain/muscle to speech disorder Case 3: One family's quest for answers • Interprofessional teams, genetic counselors, medical geneticists, research institutes • Early signs of CAS, parent education, early intervention • What about genetic testing? Q&A 3 “Genetic Causes of CAS: Case-Based Introduction to DNA, Inheritance and Clinical Management,” Presented by: Beate Peter, PhD, CCC-SLP, September 29, 2015, Sponsored by: CASANA 2 Why should you care about genetics? 4 If you are a parent of a child with childhood apraxia of speech … 5 When she was in preschool, He doesn’t have any friends. -
2019-08-03 Competition Schedule Nottwil 2019 V4.5.Xlsx
Competition Schedule Date Day Session Event Event Name Station Start 04.08.2019 Sunday 6 09:00 Women's Javelin F11-13, U20 Final 12 04.08.2019 Sunday 6 09:01 Women's Club Throw F31/32/51, U17 non-medal 11 04.08.2019 Sunday 6 09:01 Men's Club Throw F31/32/51, U20 non-medal 11 04.08.2019 Sunday 6 09:01 Women's Club Throw F31/32/51, U20 non-medal 11 04.08.2019 Sunday 6 09:25 Men's 800 m T35-38, U17 non-medal T 04.08.2019 Sunday 6 09:25 Men's 800 m T35-38, U20 non-medal T 04.08.2019 Sunday 6 09:36 Women's 800 m T35-38, U17 non-medal T 04.08.2019 Sunday 6 09:36 Women's 800 m T35-38, U20 Final T 04.08.2019 Sunday 6 09:47 Men's Shot Put F40-41, U20 Final 13 04.08.2019 Sunday 6 10:10 Men's Javelin F42-46/61-64, U20 Final 12 04.08.2019 Sunday 6 10:11 Women's 200 m T33-34, U17 non-medal T 04.08.2019 Sunday 6 10:11 Women's 200 m T33-34, U20 non-medal T 04.08.2019 Sunday 6 10:21 Men's 200 m T33-34, U20 Final T 04.08.2019 Sunday 6 10:21 Men's 200 m T33-34, U17 non-medal T 04.08.2019 Sunday 6 10:31 Women's Shot Put F40-41, U17 non-medal 13 04.08.2019 Sunday 6 10:31 Women's Shot Put F40-41, U20 Final 13 04.08.2019 Sunday 6 11:00 Women's Shot Put F32-34, U20 Victory Ceremony 30 04.08.2019 Sunday 6 11:04 Women's Javelin F11-13, U20 Victory Ceremony 30 04.08.2019 Sunday 6 11:10 Women's Shot Put F42-46/61-64, U17 Final 13 04.08.2019 Sunday 6 11:15 Men's Javelin F42-46/61-64, U17 Final 12 04.08.2019 Sunday 6 11:16 Women's 800 m T35-38, U20 Victory Ceremony 30 04.08.2019 Sunday 6 11:20 Men's Shot Put F40-41, U20 Victory Ceremony 30 04.08.2019 Sunday 6 11:30 -
Para Athletics Classification Are You, Or Do You Know Someone Who May Be, Interested in Para Athletics?
PARA ATHLETICS CLASSIFICATION ARE YOU, OR DO YOU KNOW SOMEONE WHO MAY BE, INTERESTED IN PARA ATHLETICS? Classification determines who is eligible to compete in a Para sport and then groups the eligible athletes into sport classes according to their activity limitation in a certain sport or event. Athletes are classified as “T” (Track and Jump) or “F” (Field) based on which event they are competing in, followed by a number that represents impairment type and level of impairment. For example, T12. First Letter Represents: First Number Represents: Second Number Represents: T/F TRACK OR FIELD 1-6 IMPAIRMENT TYPE 1-8 DESCRIPTION OF IMPAIRMENT Typically T identifies a track 1 = Visual Impairment The number 1 through 8 specifies event and F for a field event. 2 = Intellectual Impairment the description of the impairment as There are certain exceptions 3 = Co-ordination Impairment per the classification rules (i.e. Long Jump is a T event) 4 = Upper Limb Deficiencies; Lower Limb Deficiencies without the use of prosthetic; short stature 5 = Impaired muscle power or range of movement 6 = Limb deficiencies with the use of prosthetic PHYSICAL IMPAIRMENT SHORT STATURE F40 F41 IMPAIRED MUSCLE POWER AND/OR PASSIVE RANGE OF MOVEMENT T/F51 T/F52 T/F53 T/F54 F55 F56 F57 Athletes who compete seated LIMB DEFICIENCY T/F42 T/F43 T/F44 T/F62 T/F63 T/F64 T/F45 T/F46 T/47 Lower limb deficiency without Lower limb deficiency with Upper limb deficiency the use of a prosthetic the use of a prosthetic with or without the use of a prosthetic ATHLETES WITH ATHETOSIS, ATAXIA AND/OR -
Differential Diagnosis of Oromandibular Limb Hypogenesis Syndromes Ole Junga,B, Ralf Smeetsb, Henning Hankenb, Reinhard E
Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2016 Jun; 160(2):310-315. A patient with Charlie M Syndrome: Differential diagnosis of Oromandibular Limb Hypogenesis Syndromes Ole Junga,b, Ralf Smeetsb, Henning Hankenb, Reinhard E. Friedrichb, Max Heilandb, Amir Tagnihaa, Brian Labowa Aim. In order to provide adequate treatment to a patient with a subtype of Oromandibular Limb Hypogenesis Syndromes (OLHS), this study aimed to review and to analyze the current literature and treatment options of OLHS. Methods. Literature review in PubMed and Sciencedirect. Due to the small number of results, all available references were analyzed precisely. Results. Cases of OLHS are formerly rare and often incomplete. There are various classifications available, which, however, often seem confusing and are of little practical relevance. Furthermore, we present a complete case report of a patient with Charlie M syndrome, a type IV (Chicarilli)/ V (Hall) OLHS malformation. We also describe embryologic pathogenesis and differential diagnoses. Conclusion. As a result of our literature review, we recommend an adjusted classification for OLHS. Key words: Oromandibular Limb Hypogenesis Syndromes (OLHS), Charlie M Syndrome, Oromandibular and limb hypogenesis malformations (OLHM) Received: August 1, 2015; Accepted with revision: April 8, 2016; Available online: April 27, 2016 http://dx.doi.org/10.5507/bp.2016.020 aDepartment of Plastic and Oral Surgery, Children´s Hospital Boston, Harvard Medical School, Boston, USA bDepartment of Oral and Maxillofacial Surgery, University Medical Center Hamburg, Hamburg, Germany Corresponding author: Ole Jung, e-mail: [email protected] INTRODUCTION CASE REPORT Oromandibular Limb Hypogenesis Syndromes A twenty-three-year-old male with severe oroman- (OLHS) describe a group of heterogeneous malforma- dibular and limb deformities presented for mandibular tions of the face and body. -
N35.12 Postinfective Urethral Stricture, NEC, Female N35.811 Other
N35.12 Postinfective urethral stricture, NEC, female N35.811 Other urethral stricture, male, meatal N35.812 Other urethral bulbous stricture, male N35.813 Other membranous urethral stricture, male N35.814 Other anterior urethral stricture, male, anterior N35.816 Other urethral stricture, male, overlapping sites N35.819 Other urethral stricture, male, unspecified site N35.82 Other urethral stricture, female N35.911 Unspecified urethral stricture, male, meatal N35.912 Unspecified bulbous urethral stricture, male N35.913 Unspecified membranous urethral stricture, male N35.914 Unspecified anterior urethral stricture, male N35.916 Unspecified urethral stricture, male, overlapping sites N35.919 Unspecified urethral stricture, male, unspecified site N35.92 Unspecified urethral stricture, female N36.0 Urethral fistula N36.1 Urethral diverticulum N36.2 Urethral caruncle N36.41 Hypermobility of urethra N36.42 Intrinsic sphincter deficiency (ISD) N36.43 Combined hypermobility of urethra and intrns sphincter defic N36.44 Muscular disorders of urethra N36.5 Urethral false passage N36.8 Other specified disorders of urethra N36.9 Urethral disorder, unspecified N37 Urethral disorders in diseases classified elsewhere N39.0 Urinary tract infection, site not specified N39.3 Stress incontinence (female) (male) N39.41 Urge incontinence N39.42 Incontinence without sensory awareness N39.43 Post-void dribbling N39.44 Nocturnal enuresis N39.45 Continuous leakage N39.46 Mixed incontinence N39.490 Overflow incontinence N39.491 Coital incontinence N39.492 Postural -
Case Report Treatment of Geographic Tongue
Scholars Journal of Dental Sciences (SJDS) ISSN 2394-496X (Online) Sch. J. Dent. Sci., 2015; 2(7):409-413 ISSN 2394-4951 (Print) ©Scholars Academic and Scientific Publisher (An International Publisher for Academic and Scientific Resources) www.saspublisher.com Case Report Treatment of Geographic Tongue Superimposing Fissured Tongue: A literature review with case report Jalaleddin H Hamissi1, Mahsa EsFehani2, Zahra Hamissi3 1Associate Professor in periodontics and Dental Caries Prevention Research Center, Qazvin University Medical Sciences, Qazvin, Iran. 2Assistant Professor, Department of Oral Medicine & Diagnosis, college dentistry, Qazvin University Medical Sciences, Qazvin, Iran. 3Dental Student, College of Dentistry, Shahied Behesti University of Medical Sciences, Teheran, Iran *Corresponding author Dr Jalaleddin H Hamissi Email: [email protected] ; [email protected] Abstract: Tongue is a most sensitive part of the oral cavity. It is responsible for many functions in the mouth like swallowing, speech, mastication, speaking and breathing. Geographic tongue (Benign migratory glossitis, erythema migrans) is an asymptomatic inflammatory disorder of tongue with controversial etiology. This disease is characterized by erythematous areas showing raised greyish or white circinate lines or bands with irregular pattern on the dorsal surface of the tongue and depapillation. The objective in presenting the case report and literature review is to discuss the clinical presentation, associated causative factors and management strategies of geographic tongue. Keywords: Asymptomatic; Characteristics; Fissured tongue; Geographic tongue; Migratory INTRODUCTION in approximately three percent (3%) majority of female Geographic tongue is an asymptomatic population [9]. On other aspects of oral mucosa, such as inflammatory condition of the dorsum of tongue on commissure of lip, floor of mouth, cheek etc., which occasionally extending towards the lateral borders. -
Research on Child Mental Issues in the Field of Prevention 1. Mental
Research on child mental issues in the field of prevention Helmut Remschmidt* 1. Mental disorders / Classification, developmental aspects 2. Epidemiology and time trends 3. Types and goals of preventive interventions: risk factors and protective factors 4. Prevention programs * Prof. Helmut Remschmidt, MD, PhD, Dept. Child and Adolescent Psychiatry and Psychotherapy, Philipps-University, D-35033 Marburg (Germany) email: [email protected] A Concept of Disease/Disorder "A psychopathological disorder can be described as a state of involuntarily disturbed functions characterized by a more or less clearly defined begin, course and end preventing a child or an adolescent from taking an active part in his age-appropriate life and developmental tasks" (Remschmidt, 1988) Multiaxial System According to ICD-10 Axis 1: Clinical psychiatric syndromes Axis 2: Specific disorders of psychological development Axis 3: Intellectual level Axis 4: Medical conditions Axis 5: Associated abnormal psychosocial situations Axis 6: Global assessment of psychosocial disability Potential Relationship Between Psychopathology and Developmental Tasks (Garber, 1984) Psychopathological Developmental tasks disorder Separation anxiety Object permanence, attachment Depression Differentiation of self, self esteem, social comparison Suicide Concept of death, time perspective (future) Conduct disorder, Moral development Undersocialized Aggressive Perspective-taking, empathy Impulsivity Delay of gratification Oppositional disorder Autonomy, individuation Schizoid disorder Peer relation, friendship patterns Natural History of Tics and Associated Behaviors A Critique of Existing Classifications From a Developmental Perspective (Graham & Skuse, 1992) 1. Exclusion of causal processes 2. Disregard of the longitudinal course (example: Gilles de la Tourette-syndrome) 3. Insufficient consideration of age at onset (phases of life) 4. Insufficient judgement of developmental appropriateness of possibly abnormal behaviour (e.g. -
Therapy for Speech Sound Disorders.Pdf
2018 Fall Conference Salem, Oregon Friday, October 12, 2018 Therapy for Speech Sound Disorders: What Works and Why NSOME Don't Work Presented by: Gregory L. Lof, PhD, CCC-SLP, FASHA Educational Consultant Professor Emeritus MGH Institute of Health Professions, Boston, MA Theory and Evidence Against the Use of Nonspeech Oral Motor Exercises (NSOME) to Change Speech Sound Productions in Children Gregory L. Lof, PhD, CCC-SLP, FASHA October, 2018 Nonspeech Oral Motor Movements Defined • NSOMs are motor acts performed by various parts of the speech musculature to accomplish specific movement or postural goals that are not sufficient in themselves to have phonetic identity (Kent, 2015). Nonspeech Oral Motor Exercises (NSOME) Defined • Any technique that does not require the child to produce a speech sound but is used to influence the development of speaking abilities (Lof & Watson, 2008). • A collection of nonspeech methods and procedures that claim to influence tongue, lip, and jaw resting postures, increase strength, improve muscle tone, facilitate range of motion, and develop muscle control (Ruscello, 2008). • Oral-motor exercises (OMEs) are nonspeech activities that involve sensory stimulation to or actions of the lips, jaw, tongue, soft palate, larynx, and respiratory muscles which are intended to influence the physiologic underpinnings of the oropharyngeal mechanism and thus improve its functions. They include active muscle exercise, muscle stretching, passive exercise, and sensory stimulation (McCauley, Strand, Lof, et al., 2009). Do SLPs use NSOME? What Kind? • 85% of SLPs in the USA use NSOME to change speech sound productions (Lof & Watson, 2008); 85% of Canadian SLPs use NSOME (Hodge et al., 2005); 79% in Kentucky (Cima et al., 2009); 81% in South Carolina (Lemmon et al., 2010); 46% in Minnesota (Louma & Collins, 2012); 91% in India (Thomas & Kaipa, 2015); 49% in Australia (Rumbach, Rose, & Cheah, 2018).