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FATCO syndrome

ORPHA:2492· ICD-10 Q87.2

Definition

A rare, genetic, congenital limb malformation syndrome characterized by unilateral or bilateral fibular aplasia/hypoplasia, tibial campomelia, and lower limb oligosyndactyly involving the lateral rays. Upper limb oligosyndactyly and cleft lip/palate may also be associated.

Prevalence
<1 / 1 000 000
Age of onset
Antenatal, Neonatal