| Literature DB >> 10551509 |
S Shamsadini, H Abazardi, F Shamsadini.
Abstract
An 18-year-old girl with Leopard syndrome is described. Clinical manifestations include lentigines, ocular hypertelorism, mental and growth retardation, deafmuteness, and several patches of hair loss on her scalp. No family history of skin lentiginosis or any other inherited condition was found.Entities:
Mesh：
Year: 1999 PMID： 10551509 DOI： 10.1016/S0140-6736(99)03794-0
Source DB: PubMed Journal: Lancet ISSN： 0140-6736 Impact factor: 79.321