Monilethrix. Observation of rare hair dysplasia in two siblings. Clinical and Dermoscopic Report
DOI:
https://doi.org/10.63787/4220224859Keywords:
Monilethrix, Trichoscopy, case reportAbstract
Monilethrix is an autosomal dominant genetic hair dysplasia, rarely recessive. It is considered as a congenital pathology of the hair, having as its main characteristic a very altered hair shaft in its shape. Two cases from our file are presented: two brothers treated in 2009. Their clinical and dermatoscopic features are reviewed.
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Published
2026-07-29
How to Cite
Uraga Pazmino, E., Úraga, V., Estrella, B., López, J., & Aguilar, A. (2026). Monilethrix. Observation of rare hair dysplasia in two siblings. Clinical and Dermoscopic Report. Revista Dermatologica Centro Úraga, 4(2), 48–59. https://doi.org/10.63787/4220224859
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Case Report
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