Fibular aplasia, tibial campomelia, and oligosyndactyly syndrome
Alternate names[edit | edit source]
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[edit | edit source]
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[edit source]
Fibular aplasia, tibial campomelia, and oligosyndactyly syndrome is a rare disease.
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