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Association of Piebaldism, Multiple Café-au-lait Macules, and Intertriginous Freckling: Clinical Evidence for a Common Pathway between KIT and SPRED1

Piebaldism is a rare genodermatosis caused by KIT mutations. We report the case of a 5-year-old boy who had the white forelock and leukoderma of piebaldism, yet the diagnosis was complicated by the presence of many café-au-lait macules and axillary and inguinal freckling. Patients with similar cutan...

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Bibliografiske detaljer
Main Authors: Chiu, Yvonne E., Dugan, Stefanie, Basel, Donald, Siegel, Dawn H.
Format: Artigo
Sprog:Inglês
Udgivet: 2012
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3967413/
https://ncbi.nlm.nih.gov/pubmed/23016555
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1525-1470.2012.01858.x
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