Diprosopus

Orpha code: 1681OMIM code:

Definicja

Diprosopus is a rare, life-threatening developmental defect during embryogenesis, and a subtype of conjoined twins, characterized by partial or complete duplication of the facial structures on a single head, neck, trunk and body. It may be associated with congenital anomalies involving the cardiovascular, gastrointestinal, respiratory and central nervous systems. Cleft lip and palate have been reported in rare cases.

Disease data
Klasyfikacja

Morphological anomaly

Synonimy
Craniofacial duplication
Diprosopia
Kod ORPHA
1681
Kod OMIM
-
Kod ICD10
Q89.4
Kod ICD11
-

No additional description.

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