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Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

A Turkish woman has a hair condition caused by a LIPH gene mutation.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

A new genetic variant in the LIPH gene causes hair growth issues in a Chinese patient.

A specific gene mutation causes different hair defects in Indian monilethrix families.

The document concludes that the girl's hairlessness is likely inherited from her parents.

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

Tissue-specific variation in mutant load complicates genetic counseling and prenatal diagnosis.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

Specific keratin gene mutations can cause monilethrix.

The gene for Clouston syndrome in a large Indian family is located in the 13q11-q12.1 region.

Researchers found a new mutation causing total hair loss from birth.

Mutations in the hairless gene cause a rare form of permanent hair loss.

Polycystic ovaries and early male baldness are inherited traits.

Cronkhite-Canada syndrome can cause multiple gastrointestinal polyps and various physical symptoms.

A new genetic mutation linked to Hutchinson-Gilford progeria syndrome was found in China.

Uncombable hair is inherited dominantly with complete penetrance.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

Autoimmune gastritis is a common cause of iron deficiency and should be included in diagnostic guidelines.

Androgenetic alopecia is a long-term, immune-related disorder that starts during puberty due to androgen secretion, and it might be improved with iron tablets, platelet transfusion, and anti-inflammation therapy.

The HSD3B1 variant increases hair loss risk in overweight women with PCOS.

Iron deficiency is common in kidney transplant patients, and while iron treatment helps, it can cause high red blood cell levels.

A father and son in Yemen have a genetic condition causing hair loss and nail problems.

A new genetic mutation causes severe Leydig cell hypoplasia, affecting sexual development.

Isolated patchy heterochromia with pili annulati can occur without other health issues.

Mutations in the LIPH gene cause woolly hair in a child.

A specific gene mutation causes congenital hair loss.