Linear and whorled naevoid hypermelanosis: a case with systemic involvement and trisomy 18 mosaicism.
case_report · Level V
Where this comes from
- Record sourced from PubMed, PMID 11952553.
- 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
We describe a 20-year-old woman with trisomy 18 mosaicism, who presented with skeletal anomalies, epilepsy, mental retardation, and linear and whorled naevoid hypermelanosis.
Medical subject headings
- Bone Diseases, Developmental
- Chromosomes, Human, Pair 18
- Pigmentation Disorders
- Trisomy