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Hirschsprung disease-type D brachydactyly syndrome

ORPHA:2150· ICD-10 Q43.1

Definition

Hirschsprung disease-type D brachydactyly syndrome is characterized by Hirschsprung disease and absence or hypoplasia of the nails and distal phalanges of the thumbs and great toes (type D brachydactyly). It has been described in four males from one family (two brothers and two maternal uncles). Transmission appears to be X-linked recessive but autosomal dominant inheritance with incomplete penetrance in females can not be ruled out.

Prevalence
<1 / 1 000 000
Age of onset
Neonatal