Splenogonadal fusion-limb defects-micrognathia syndrome

Orpha code: 2063OMIM code: 183300

Definicja

A rare dysostosis syndrome characterized by abnormal fusion of the spleen with the gonad (or more rarely with remnants of the mesonephros), limb abnormalities (consisting of amelia or severe reduction defects leading to upper and/or lower rudimentary limbs) and orofacial abnormalities such as cleft palate, bifid uvula, microglossia and mandibular hypoplasia. It could also be associated with other malformations such as cryptorchidism, anal stenosis/atresia, hypoplastic lungs and cardiac malformations.

Disease data
Klasyfikacja

Malformation syndrome

Synonimy
SGFLD syndrome
Kod ORPHA
2063
Kod OMIM
183300
Kod ICD10
Q87.8
Kod ICD11
-

No additional description.

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