9780769300191

Syndrome Identification for Speech-Language Pathology An Illustrated Pocketguide

by
  • ISBN13:

    9780769300191

  • ISBN10:

    0769300197

  • Edition: 1st
  • Format: Paperback
  • Copyright: 1999-11-19
  • Publisher: Cengage Learning

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Supplemental Materials

What is included with this book?

Summary

This book provides a synopsis of the important communicative impairments associated with 160 multiple anomaly syndromes likely to be encountered by speech-language pathologists. It describes the types of speech, voice, resonance, language, and cognitive disorders associated with each syndrome and provides up-to-date information about the etiology of each of the disorders. Summarized for each entry are a listing of the anomalies associated with the syndromes, the natural history of the disorder, and the treatment prognosis, which allows proper choices of treatment plans, and differential diagnosis. This handy pocket reference is liberally illustrated with examples of the many syndromes described.

Author Biography

Robert I. Shprintzen, Ph.D., is Director of Communication Disorders Unit and Professor of Otolaryngology and Communication Science, State University of New York Health Sciences Center at Syracuse. He also directs the Center for Genetic Communication Disorders and the Center for Diagnosis, Treatment, and Study of Velo-Cardio-Facial Syndrome.

Table of Contents

Preface ix
Acknowledgments xii
How to Use This PocketGuide xiii
Syndromes With Speech, Language and Cognitive Impairments
Aarskog Syndrome
1(3)
Aase-Smith Syndrome
4(2)
Abruzzo-Erickson Syndrome
6(2)
Achondroplasia
8(3)
Acrocallosal Syndrome
11(3)
Acrodysostosis
14(2)
AEC Syndrome
16(2)
Aicardi Syndrome
18(2)
Alagille Syndrome
20(3)
Albers-Schonberg Syndrome
23(2)
Angelman Syndrome
25(3)
Antley-Bixler Syndrome
28(3)
Apert Syndrome
31(4)
Ascher Syndrome
35(2)
Ataxia-telangiectasia Syndrome
37(3)
Baller-Gerold Syndrome
40(3)
Bamatter Syndrome
43(2)
Bannayan-Zonana Syndrome
45(3)
Bardet-Biedl Syndrome, Type 1
48(2)
Bardet-Biedl Syndrome, Type 2
50(2)
Bardet-Biedl Syndrome, Type 3
52(2)
Bardet-Biedl Syndrome, Type 4
54(2)
Basal Cell Nevus Syndrome
56(2)
Beckwith-Wiedemann Syndrome
58(4)
Bencze Syndrome
62(2)
Berardinelli Syndrome
64(3)
Binder Syndrome
67(2)
Blepharonasofacial Syndrome
69(2)
Bloom Syndrome
71(2)
BOF Syndrome
73(2)
BOR Syndrome
75(3)
Borjeson-Forssman-Lehmann Syndrome
78(2)
Brachial Plexus Neuropathy
80(2)
C Syndrome
82(2)
Campomelic Dysplasia
84(2)
Cardiofaciocutaneous Syndrome
86(2)
Carpenter Syndrome
88(3)
Cartilage-Hair Hypoplasia
91(2)
Cat Eye Syndrome
93(3)
Catel-Manzke Syndrome
96(2)
Cerebocostomandibular Syndrome
98(3)
Cerebrooculofacioskeletal Syndrome
101(2)
CHARGE Association
103(3)
Christian Syndrome
106(3)
Cleidocranial Dysplasia
109(3)
Clouston Syndrome
112(2)
Cockayne Syndrome
114(2)
Cockayne Syndrome, Type II
116(2)
Cockayne Syndrome, Type III
118(2)
Coffin-Lowry Syndrome
120(2)
Coffin-Siris Syndrome
122(2)
Cohen Syndrome
124(2)
Cowden Syndrome
126(2)
Craniodiaphyseal Dysplasia
128(3)
Craniofrontonasal Syndrome
131(2)
Craniometaphyseal Dysplasia
133(2)
Cri-du-Chat Syndrome
135(2)
Crouzon Syndrome
137(3)
Cryptophthalmos Syndrome
140(2)
De Barsy Syndrome
142(2)
de Lange Syndrome
144(4)
Diastrophic Dysplasia
148(2)
Distal Arthrogryposis
150(2)
Down Syndrome
152(4)
Dubowitz Syndrome
156(3)
Dysautonomia
159(2)
Dyskeratosis Congenita
161(2)
Dysosteosclerosis
163(2)
EEC Syndrome
165(3)
Ellis-van Creveld Syndrome
168(2)
Escobar Syndrome
170(3)
Fabry Syndrome
173(2)
Facio-cardio-renal Syndrome
175(2)
Facioscapulohumeral Muscular Dystrophy
177(2)
Femoral Hypoplasia Unusual Facies Syndrome
179(3)
Fetal Alcohol Syndrome
182(4)
FG Syndrome
186(3)
Filiform Adhesions and Cleft Lip-Palate
189(2)
Freeman-Sheldon Syndrome
191(3)
Frontometaphyseal Dysplasia
194(3)
GAPO Syndrome
197(2)
Golabi-Rosen Syndrome
199(3)
Goldberg-Shprintzen Syndrome
202(2)
Goltz Syndrome
204(3)
Hajdu-Cheney Syndrome
207(3)
Hallerman-Streiff Syndrome
210(3)
Hecht Syndrome
213(2)
Hemihypertrophy
215(2)
Herrmann Syndrome
217(2)
HMC Syndrome
219(2)
Holoprosencephaly
221(4)
Homocystinuria
225(2)
Hunter Syndrome
227(3)
Hurler Syndrome
230(3)
Hypochondroplasia
233(2)
Hypohidrotic Ectodermal Dysplasia
235(3)
Jackson-Weiss Syndrome
238(2)
Johanson-Blizzard Syndrome
240(2)
Johnson-McMillin Syndrome
242(2)
Kallmann Syndrome
244(2)
Kartagener Syndrome
246(2)
Kearns-Sayre Syndrome
248(2)
Keutel Syndrome
250(2)
Klippel-Trenaunay-Weber Syndrome
252(2)
Kniest Syndrome
254(3)
Laband Syndrome
257(3)
Langer-Giedion Syndrome
260(2)
Larsen Syndrome
262(2)
Laurence-Moon Syndrome
264(2)
Lenz Syndrome
266(3)
Lenz-Majewski Syndrome
269(2)
Lesch-Nyhan Syndrome
271(2)
Lowe Syndrome
273(2)
Maffucci Syndrome
275(2)
Mannosidosis
277(3)
Marden-Walker Syndrome
280(3)
Marfan Syndrome
283(2)
Marinesco-Sjogren Syndrome
285(2)
Maroteaux-Lamy Syndrome
287(2)
Marshall Syndrome
289(2)
Marshall-Smith Syndrome
291(2)
Mohr Syndrome
293(3)
Morquio Syndrome
296(2)
Multiple Lentigines Syndrome
298(2)
Nager Syndrome
300(3)
Neurofibromatosis, Type I
303(3)
Niikawa-Kuroki Syndrome
306(3)
Noonan Syndrome
309(4)
Oculo-Auriculo-Vertebral Dysplasia (or Spectrum)
313(5)
Oculocerebrocutaneous Syndrome
318(2)
Oculo-Dento-Digital Syndrome
320(2)
Oculopharyngeal Muscular Dystrophy
322(2)
Opitz Syndrome
324(3)
Oral-Facial-Digital Syndrome
327(3)
Otopalatodigital Syndrome Type 1
330(3)
Otopalatodigital Syndrome Type 2
333(3)
Pena-Shokeir Syndrome
336(3)
Pfeiffer Syndrome
339(3)
Pontobulbar Palsy With Sensorineural Hearing Loss
342(2)
Popliteal Ptergium Syndrome
344(2)
Prader-Willi Syndrome
346(3)
Proteus Syndrome
349(3)
Pycnodysostosis
352(2)
Rapp-Hodgkin Syndrome
354(3)
Robinow Syndrome
357(3)
Rubinstein-Taybi Syndrome
360(4)
Saethre-Chotzen Syndrome
364(2)
Sanfilippo Syndrome
366(3)
Seitelberger Syndrome
369(2)
Setleis Syndrome
371(2)
Short Syndrome
373(3)
Shprintzen-Goldberg Syndrome
376(4)
Smith-Lemli-Optiz Syndrome
380(3)
Sotos Syndrome
383(2)
Spondyloepiphyseal Dysplasia Congenita
385(3)
Steinert Syndrome
388(4)
Strickler Syndrome
392(4)
Sturge-Weber Syndrome
396(2)
Treacher Collins Syndrome
398(4)
Turner Syndrome
402(3)
Van Buchem Syndrome
405(3)
van der Woude Syndrome
408(3)
Velo-Cardio-Facial Syndrome (VCFS)
411(6)
Weaver Syndrome
417(3)
Wildervanck Syndrome
420(3)
Williams Syndrome
423(3)
Wolf-Hirschhorn Syndrome
426(2)
X-Linked Mental Retardation
428(3)
Index 431

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