SCARF syndrome
| SCARF syndrome | |
|---|---|
| Classification and external resources | |
| OMIM | 312830 |
SCARF syndrome is a rare syndrome characterized by skeletal abnormalities, cutis laxa, craniostenosis, ambiguous genitalia, retardation, and facial abnormalities. It shares some features with Lenz-Majewski hyperostotic dwarfism syndrome.
References
- Koppe R, Kaplan P, Hunter A, MacMurray B (1989). "Ambiguous genitalia associated with skeletal abnormalities, cutis laxa, craniostenosis, psychomotor retardation, and facial abnormalities (SCARF syndrome).". Am J Med Genet. 34 (3): 305–12. doi:10.1002/ajmg.1320340302. PMID 2596519.
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