Autosomal Dominant Monilethrix With Incomplete Penetrance Due to a Novel KRT86 Mutation in a Chinese Family
April 2024
in “
Anais Brasileiros de Dermatologia
”
Research cited in this study
5 / 5 resultsresearch Autosomal Recessive Monilethrix: Novel Variants of the DSG4 Gene in Three Chinese Families
New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.
research A Novel Monilethrix Mutation in Coil 2A of KRT86 Causing Autosomal Dominant Monilethrix with Incomplete Penetrance
A new mutation in the KRT86 gene causes a hair disorder with variable expression.
research Congenital Hair Loss Disorders: Rare, But Not Too Rare
Some hair loss disorders are caused by genetic mutations affecting hair growth.
research De Novo Mutations in Monilethrix
Specific keratin gene mutations can cause monilethrix.