Monilethrix. Observation of rare hair dysplasia in two siblings. Clinical and Dermoscopic Report

Authors

  • Enrique Úraga P. Centro Dermatológico Dr Uraga
  • Verónica Úraga Centro Dermatológico Dr Uraga
  • Belén Estrella Centro Dermatológico Dr Uraga
  • Jessica López Centro Dermatológico Dr Uraga
  • Andrea Aguilar Centro Dermatológico Dr Uraga

DOI:

https://doi.org/10.63787/4220224859

Keywords:

Monilethrix, Trichoscopy, case report

Abstract

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.

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