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This encyclopedic work describes the phenotype spectrum, epidemiology, mode of inheritance, and pathogenesis of nearly 700 genetic syndromes. Uniquely comprehensive, it depicts the clinical features of all known genetic disorders affecting the head and neck and contains over 2300 illustrations. The authors make a clear distinction between doubtful and authentic cases, and bibliographies accompany each syndrome to encourage further research. This is a reorganized, completely rewritten and greatly expanded version of the second edition. It will be an invaluable guide for all clinicians dealing with patients who have head and neck syndromes.
This text serves as a comprehensive clinical reference for the identification, classification, and understanding of nearly 700 genetic syndromes affecting the head and neck. The authors, L. Stefan Levin, M. Michael Cohen Jr., and Robert J. Gorlin, leverage their extensive expertise in medical genetics to provide a systematic framework for diagnosing complex phenotypic presentations. By synthesizing epidemiological data, inheritance patterns, and pathogenesis, the work establishes a rigorous standard for clinical evaluation and differential diagnosis in the field of craniofacial genetics.
What You Will Find
Clinicians and geneticists regard this volume as a foundational reference for the diagnosis of complex craniofacial disorders. The text is noted for its high density of clinical information and its systematic approach to distinguishing between authentic and questionable diagnostic cases.
Page Count:
1008
Publication Date:
1990-06-28
Publisher:
Oxford University Press
ISBN-10:
0195045181
ISBN-13:
9780195045185
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