Monilethrix

Monilethrix
Classification and external resources
Specialty
ICD-10	Q84.1 (ILDS Q84.140)
ICD-9-CM	757.4
OMIM	158000
DiseasesDB	29592
eMedicine	derm/763
Patient UK	Monilethrix

Monilethrix (also referred to as beaded hair) is a rare autosomal dominant hair disease that results in short, fragile, broken hair that appears beaded. It comes from the Latin word for necklace (monile) and the Greek word for hair (thrix).

Characteristics

The presentation may be of alopecia (baldness). Individuals vary in severity of symptoms. Nail deformities may also be present as well as hair follicle keratosis and follicular hyperkeratosis.

Cause and Genetics

Monilethrix has an autosomal dominant pattern of inheritance.

Monilethrix is caused by mutations affecting the genes KRTHB1 (KRT81), KRTHB3 (KRT83), or KRTHB6 (KRT86) which code for type II hair cortex keratins. The disorder is inherited in an autosomal dominant manner. This means that the defective gene(s) responsible for the disorder is located on an autosome, and only one copy of the gene is sufficient to cause the disorder, when inherited from a parent who has the disorder.

Diagnosis

Monilethrix may be diagnosed with trichoscopy

See also

• List of cutaneous conditions
• List of conditions caused by problems with junctional proteins
• List of cutaneous conditions caused by mutations in keratins