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Grant syndrome
rareGrant 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.
- Identifiers
- MONDO:0007683 OMIM:138930Orphanet:2097
- Part of
- Hereditary disease
- Also known as
- persistent wormian bones, blue sclerae, mandibular hypoplasia, shallow glenoid fossae and campomelia
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