FATCO syndrome

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.

Fibular hypoplasia

Underdevelopment of the fibula.


合計: 2

                       


（表示件数）
PMID (PMCID)
30151452
(6100663)
 OTHER
A Female Newborn Infant with FATCO Syndrome Variant (Fibular Hypoplasia, Tibial Campomelia, Oligosyndactyly) - A Case Report.
Smets G, Vankan Y, Demeyere A.
J Belg Soc Radiol. 2016;100(1):41.
A Female Newborn Infant with FATCO Syndrome Variant (Fibular Hypoplasia, Tibial Campomelia, Oligosyndactyly) - A Case Report.
25386471
 OTHER
FATCO Syndrome Variant - Fibular Hypoplasia, Tibial Campomelia and Oligosyndactyly -- A Case Report.
Goyal N, Kaur R, Gupta M, Bhatty S, Paul R.
J Clin Diagn Res. 2014;8(9):LD01-2.
FATCO Syndrome Variant - Fibular Hypoplasia, Tibial Campomelia and Oligosyndactyly -- A Case Report.