Speckled acral hypopigmentation in an adolescent
Author:
Affiliation:
1. Dermatology Residency Program; Lehigh Valley Health Network; Allentown PA USA
2. Department of Dermatology; Pennsylvania State University; Hershey PA USA
Publisher
Wiley
Subject
Dermatology,Pediatrics, Perinatology and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/pde.13341/fullpdf
Reference5 articles.
1. Familial speckled acral hypopigmentation: a new variant of reticulate acropigmentation?;Malakar;Indian J Dermatol Venereol Leprol,2005
2. Dyschromatosis symmetrica hereditaria: a retrospective case series and literature review;Peng;Dermatol Sin,2013
3. Dyschromatosis symmetrica hereditaria with long hair on the forearms, hypo/hyperpigmented hair, and dental anomalies: report of a novel ADAR1 mutation;Kantaputra;Am J Med Genet A,2012
4. Dowling-Degos disease with mutations in POFUT1 is clinicopathologically distinct from reticulate acropigmentation of Kitamura;Kono;Br J Dermatol,2015
5. Whole-exome sequencing identified ADAM10 mutations as a cause of reticulate acropigmentation of Kitamura, a clinical entity distinct from Dowling-Degos disease;Kono;Hum Mol Genet,2013
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1. Acral Speckled Hypomelanosis: A Case Report and a Review of Literature;The American Journal of Dermatopathology;2023-04-10
2. Miscellaneous Hypomelanoses and Hypochromia;Atlas of Pigmentary Skin Disorders;2023
3. A rare case of unilateral acral speckled hypopigmentation;International Journal of Dermatology;2021-12-05
4. Acral speckled hypomelanosis;JAAD Case Reports;2019-09
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