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

The man has a genetic skin condition called pachyonychia congenita.

Pseudopelade is a rare inherited hair loss condition with a genetic cause.

A Chinese family had a child with a specific gene mutation causing vitamin D-resistant rickets, but the child improved with calcium and low-dose calcitriol.

The conclusion is that there might be a link between certain types of baldness and prostate cancer, which could be due to shared hormonal pathways.

A new type of hereditary hair loss in a Chinese family is linked to chromosome 2p25.1–2p23.2.

Mutations in the PADI3 gene are linked to a higher risk of scarring hair loss in women of African descent.

The boy's genetic diagnosis of ectodermal dysplasia helped improve management and counseling for him and his sister.

Male gender and family history predict alopecia areata recurrence.

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

Genetic factors and diet significantly increase the risk of male pattern baldness.

Men with male pattern baldness may have a slightly higher risk of prostate cancer.

Low-penetration genes might help personalize colorectal cancer prevention.

Oxidative stress increases in early hair loss, and family history plays a role; antioxidants may help future treatments.

Clouston syndrome is inherited in an autosomal dominant pattern and caused by a specific gene mutation, with no current treatment available.

A specific gene mutation in Japanese people can cause varying degrees of hair thinning in adulthood.

Early hair loss may predict heart disease.

A certain mutation in the fetal alpha 5-reductase gene is linked to a higher risk of late miscarriage.

The C-allele and CC-genotype in the PTPN22 gene lower the risk of alopecia areata.

A rare genetic mutation in the EGFR gene caused severe skin issues and other health problems in a Slovakian girl, who is now 4 years old and receiving care.

Genetics likely cause premature graying hair, not vitamin levels.

Diagonal earlobe and preauricular creases may indicate higher coronary artery disease risk in men.

Men with baldness are more prone to skin cancers on the scalp due to sun exposure, not testosterone.

PDCD4 protein levels, affected by genetics and breastfeeding, may predict breast cancer treatment response.

A six-year-old boy with excessive hair growth and other symptoms may have a genetic link on chromosome 17q, requiring regular medical follow-ups.

Men with melanoma have a higher risk of later being diagnosed with prostate cancer.

Certain genetic variations in the RAB5B gene are linked to a higher risk of polycystic ovary syndrome in Chinese Han women.

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

Excess maternal androgens can cause heart problems in offspring.