| Literature DB >> 21165217 |
Jong Hoon Won1, Min Jung Lee, Joon Soo Park, Hyun Chung, Jin Kyung Kim, Jeong Su Shim.
Abstract
Lowe syndrome is a rare genetic disease that appears to cause various clinical symptoms involving the eye, nervous system, and kidney. While a mutation of the OCRL1 gene is known to be responsible for this syndrome, the exact pathophysiology remains unclear. Various multi-organ symptoms are characteristic of Lowe syndrome, but skin lesions have rarely been described. Recently, mechanisms for the association of Lowe syndrome and skin lesions have been proposed. We report this case of Lowe syndrome involving multiple epidermal cysts on the scalp in a 6-year-old male child.Entities:
Keywords: Epidermal cyst; Lowe syndrome
Year: 2010 PMID: 21165217 PMCID: PMC2991724 DOI: 10.5021/ad.2010.22.4.444
Source DB: PubMed Journal: Ann Dermatol ISSN: 1013-9087 Impact factor: 1.444