Grant syndrome
Alternate names[edit | edit source]
Persistent wormian bones, blue sclerae, mandibular hypoplasia, shallow glenoid fossae and campomelia
Definition[edit | edit source]
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.
NIH genetic and rare disease info[edit source]
Grant syndrome is a rare disease.
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