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The Russell–Silver Syndrome: A Case Report and Brief Review of the Literature
Author(s) -
Perkins CPT Robert M.,
HoangXuan Maj Tuan A.
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.1525-1470.2002.00230.x
Subject(s) - medicine , dermatology , craniofacial , psychiatry
The Russell–Silver syndrome's phenotypic features consist of musculoskeletal abnormalities, genitourinary malformations, craniofacial dysmorphy and cutaneous dyschromia, which is usually reported as café au lait spots. We present the first instances of a large, unilateral, achromic patch as an additional cutaneous manifestation of the Russell–Silver syndrome.