Učitavanje...
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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| Glavni autori: | , , , |
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| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
2012
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| Teme: | |
| Online pristup: | 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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