research Monilethrix
A 12-year-old girl was diagnosed with monilethrix, a genetic condition causing fragile, beaded hair that breaks easily, with no effective treatment available.
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5 / 84 results research Sequence Data and Chromosomal Localization of Human Type I and Type II Hair Keratin Genes
Human hair keratin genes hHa2 and hHb1 are located on chromosomes 17 and 12.
research A Variable Monilethrix Phenotype Associated With a Novel Mutation, Glu402Lys, in the Helix Termination Motif of the Type II Hair Keratin hHb1
A new mutation, Glu402Lys, in hair keratin is linked to variable symptoms of monilethrix.
research Recurrent Missense Mutations in the Hair Keratin Gene HHb6 in Monilethrix
Mutations in the hHb6 gene cause the hair disorder monilethrix.
research Detection of Type II Hair Keratin Gene in a Family with Monilethrix
A unique gene mutation was found in a family with monilethrix.
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