Synonyms: Fibular aplasia-tibial campomelia-oligosyndactyly syndrome | Hecht-Scott 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.
Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview. Reference: Access aggregated data from Orphanet at Orphadata. Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http://www.orphadata.org. Data version April 2026
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