Waardenburg syndrome [electronic resource] /
Series: Genetic syndromes and communication disorders seriesPublication details: San Diego : Plural Pub., 2007.Description: 1 online resource (xiv, 136 pages) : illustrations (chiefly color)Content type:- text
- computer
- online resource
- 9781597567626
- 1597567620
- 2006 J-493
- WV 270
- digitized HathiTrust Digital Library committed to preserve
Item type | Home library | Class number | URL | Status | Date due | Barcode | |
---|---|---|---|---|---|---|---|
Electronic book | Stenhouse Library | Link to resource | Available |
Includes bibliographical references and index.
Waardenburg syndrome types 1 and 3 -- Waardenburg syndrome types 2 and 4 -- Differential diagnosis of Waardenburg syndrome -- Audiologic assessment and treatment of Waardenburg syndrome / Kathleen Hutchinson -- Counseling families with Waardenburg syndrome-related hearing loss -- Treatment issues for patients with Waardenburg syndrome.
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Master and use copy. Digital master created according to Benchmark for Faithful Digital Reproductions of Monographs and Serials, Version 1. Digital Library Federation, December 2002. MiAaHDL
http://purl.oclc.org/DLF/benchrepro0212
digitized HathiTrust Digital Library committed to preserve pda MiAaHDL
Print version record.
From the Publisher: Waardenburg syndrome often goes undetected and undiagnosed as many healthcare professionals are unaware of this syndrome. This text represents the first publication dedicated entirely to Waardenburg syndrome and is an essential resource for identification, diagnosis, and treatment. It introduces basic genetic concepts, explains the four types of Waardenburg syndrome, and provides practical guidance in recognizing individuals with the syndrome, including color photographs that highlight diagnostic features and incidence of the syndrome in families, testing for hearing, and counseling patients and parents. It then provides a comprehensive plan of action for treating patients, and encourages readers to understand when and how to appropriately refer patients to the craniofacial team for genetic assessment. Resource materials for both clinicians and clients are also included.
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