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[Acrocephalosyndactylia--Vogt syndrome]
Psychiatrie, Neurologie, Und Medizinische Psychologie
|June 1, 1985
Summary
This study describes a rare Vogt syndrome case, a combination of Apert and Crouzon syndromes, with associated dysraphia syndrome. The findings highlight complex genetic and potential environmental factors in craniofacial malformations.
Area of Science:
- Medical Genetics
- Developmental Biology
- Clinical Dysmorphology
Background:
- Vogt syndrome is a rare condition combining Apert syndrome and Crouzon syndrome.
- Craniofacial malformations present significant challenges in diagnosis and management.
- Understanding the etiology of complex syndromes is crucial for genetic counseling and treatment.