Premium
Dyschromatosis Universalis Hereditaria: Report of a case and Review of the Literature
Author(s) -
Al Hawsawi Khalid,
Al Aboud Khalid,
Ramesh V.,
Al Aboud Daifullah
Publication year - 2002
Publication title -
pediatric dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.542
H-Index - 73
eISSN - 1525-1470
pISSN - 0736-8046
DOI - 10.1046/j.1525-1470.2002.00225.x
Subject(s) - medicine , girl , dermatology , alopecia universalis , pediatrics , genetics , hair loss , biology
We describe dyschromatosis universalis in a 19‐month‐old Saudi Arabian girl. She had no associated defects and none of the other family members were affected. Similar cases reported from countries other than the Far East, where the disease was first described, are discussed.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom