Fibular aplasia, tibial campomelia, and oligosyndactyly syndrome

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Alternate names

FATCO syndrome; Terminal transverse defects of the limbs associated with congenital heart malformations; Hecht-Scott syndrome; Limb deficiency-heart malformation syndrome; Fibular aplasia-tibial campomelia-oligosyndactyly syndrome

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.

NIH genetic and rare disease info

Fibular aplasia, tibial campomelia, and oligosyndactyly syndrome is a rare disease.

Rare and genetic diseases

Rare diseases - Fibular aplasia, tibial campomelia, and oligosyndactyly syndrome

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Contributors: Deepika vegiraju, Prab R. Tumpati, MD