Acrofacial dysostosis, Weyers type
ORPHA:952· ICD-10 Q75.4
Definition
A rare ectodermal dysplasia syndrome with bone abnormalities characterized by onychodystrophy; anomalies of the lower jaw, oral vestibule and dentition; post-axialpolydactyly; moderately restricted growth with short limbs; and normal intelligence. Although it closely resembles Ellis-van Creveld syndrome, an allelic disorder and another type of ciliopathy, WAD is usually a milder disease without the presence of heart abnormalities and is inherited in an autosomal dominant manner.
- Prevalence
- Unknown
- Inheritance
- Autosomal dominant
- Age of onset
- Neonatal