Grant syndrome

Orpha code: 2097OMIM code: 138930

Definition

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
Classification

Malformation syndrome

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

No additional description.

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