Grant syndrome

Orpha code: 2097OMIM code: 138930

Definicja

Grant syndrome is a rare osteogenesis imperfecta-like disorder, described in two patients to date, characterized clinically by persistent wormian bones, blue sclera, mandibular hypoplasia, shallow glenoid fossa, and campomelia. There have been no further descriptions in the literature since 1986.

Disease data
Klasyfikacja

Malformation syndrome

Kod ORPHA
2097
Kod OMIM
138930
Kod ICD10
Q87.5
Kod ICD11
LD24.KY

No additional description.

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