Fibular dimelia-diplopodia syndrome

Orpha code: 1757OMIM code:

Definition

A very rare, genetic, congenital limb malformation syndrome characterized by duplication of the fibula associated with pre-axial mirror polydactyly of the foot, that may occur as an isolated malformation or be assoicated with other anomalies, including ulnar dimelia, facial abnormalities and sacrococcygeal teratoma.

Disease data
Classification

Malformation syndrome

Synonyms
Leg duplication-mirror foot syndrome
Zdwojenie nogi - lustrzane odbicie stopy
ORPHA code
1757
OMIM code
-
ICD10 code
Q74.8
ICD11 code
-

No additional description.

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