Type 2 segmental acanthosis nigricans: A historical case explained by a new concept

Archives of Dermatology

Volumn 144, Issue 12, 2008, Pages 1637-

  Happle, Rudolf ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

FIBROBLAST GROWTH FACTOR RECEPTOR 3;

ACANTHOSIS NIGRICANS; ADOLESCENT; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CASE REPORT; CLINICAL FEATURE; GENE MUTATION; GENODERMATOSIS; HETEROZYGOSITY LOSS; HUMAN; MALE; NEUROFIBROMATOSIS; NEVUS; PRIORITY JOURNAL; SKIN BIOPSY; SKIN DEFECT;

ABDOMEN; ACANTHOSIS NIGRICANS; ADOLESCENT; FUNCTIONAL LATERALITY; GROIN; HISTORY, 20TH CENTURY; HUMANS; LOSS OF HETEROZYGOSITY; MALE; RECEPTOR, FIBROBLAST GROWTH FACTOR, TYPE 3;

EID: 58049221002     PISSN: 0003987X     EISSN: 15383652     Source Type: Journal    
DOI: 10.1001/archderm.144.12.1637     Document Type: Article

References (6)

1. Curth HO. Benign type of acanthosis nigricans: etiology. Arch Dermatol. 1936;34:353-366.
2. Curth HO, Aschner BM. Genetic studies on acanthosis nigricans. Arch Dermatol. 1959;79(1):55-66.
3. Curth HO. Unilateral epidermal naevus resembling acanthosis nigricans. Br J Dermatol. 1979;95(4):433-436.
4. Happle R. Loss of heterozygosity in human skin. J Am Acad Dermatol. 1999;41(2, pt 1):143-161.
5. Berk DR, Spector EB, Bayliss SJ. Familial acanthosis nigricans due to K650T FGFR3 mutation. Arch Dermatol. 2007;143(9):1153-1156.
6. Ersoy-Evans S, Sahin S, Mancini AJ, et al. The acanthosis nigricans form of epidermal nevus. J Am Acad Dermatol. 2006;55(4):696-698.