WebSummary. Monilethrix is a rare condition caused by a defect in the hair shaft resulting in hair which appears dry, dull, and brittle, and which breaks spontaneously or with mild trauma. The severity and course may vary from person to person. Members of the medical team for Monilethrix may include: Primary care … Rare diseases are not rare. About 30 million people in the U.S. are affected by a rare … WebDescription of the case of monilethrix in 3 years old child. Description of the case of monilethrix in 3 years old child. Tetiana V . Svyatenko. 2016, Global Dermatology. See Full PDF Download PDF.
Monilethrix: a rare hereditary condition - PubMed
WebMay 27, 2016 · Monilethrix is an autosomal dominant genodermatosis characterized by hair fragility, keratosis pilaris, and pathognomonic beading of the hair shaft. Hair fragility may lead to hair breakage and the appearance of generalized hair loss. The gene for autosome-dominant monilethrix has been mapped to the epithelial keratin gene cluster on 12q13, 2 WebMay 20, 2024 · Description of hair loss; Medical and family history; PHYSICAL EXAMINATION. Scalp and hair examination - Visual inspection - Trichoscopy - Hair pull … philips customer service canada
A Variable Monilethrix Phenotype Associated With a
WebFeb 11, 2024 · Monilethrix is a rare hereditary hair loss disorder characterized by hair fragility and beaded hair shaft alterations, and it could be an autosomal dominant or autosomal recessive trait. We reported three cases of AR form of monilethrix and identified four novel variants in the DSG4 gene, including a large deletion mutation, could provide ... WebDescription. Monilethrix is a rare genodermatosis characterized by a hair shaft dysplasia resulting in hypotrichosis. Genes related to Monilethrix. DSG4 KRT81 KRT83 KRT86 View recommended genes panels. Clinical Features Top most frequent phenotypes and symptoms related to Monilethrix Webfrom monilethrix during his childhood but did not mention the presence of monilethrix in previous gen-erations. The father had a normal physical appearance and normal scalp hair. JS had keratosis pilaris, which is a common fea-ture of this condition. His hair was brittle and broke easily. Improvement has been seen during the sum- philips customer service australia