Microcornea-glaucoma-absent frontal sinuses syndrome

Orpha code: 2536OMIM code: 156700

Definicja

A rare developmental defect during embryogenesis syndrome characterized by the association of microcornea, glaucoma and frontal sinus hypoplasia. Thick palmar skin and torus palatinus have also been reported. There have been no further descriptions in the literature since 1995.

Disease data
Klasyfikacja

Malformation syndrome

Kod ORPHA
2536
Kod OMIM
156700
Kod ICD10
Q15.8
Kod ICD11
-

No additional description.

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