vitalwiki

Diaphragmatic defect-limb deficiency-skull defect syndrome

ORPHA:2141· ICD-10 Q87.8

Definition

A rare genetic multiple congenital anomalies/dysmorphic syndrome characterized by diaphragmatic hernia, lung hypoplasia, ossification defect of the skull, and severe limb hypoplasia. Other clinical features may include, syndactyly, clinodactyly, extra spleen, absence of the femur or pelvic bone, partial intestinal malrotation, omphalocele and testicular atrophy.

Prevalence
<1 / 1 000 000
Inheritance
Unknown
Age of onset
Antenatal