Синдром Гранта
ORPHA:2097· ICD-10 Q87.5· Grant syndrome
Визначення(English summary)
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.
- Поширеність
- <1 / 1 000 000
- Успадкування
- Unknown
- Вік початку
- Neonatal