Leopard syndrome.
case_report · Level V
Where this comes from
- Record sourced from PubMed, PMID 10551509.
- No licence information is recorded for this record.
- Because redistribution is not established, this page shows the abstract only. Follow the links below for the full text.
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.
Medical subject headings
- Abnormalities, Multiple
- Deafness
- Hypertelorism
- Lentigo