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A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

DTC hair regrowth solutions are improving hair health and confidence with innovative, personalized approaches.

Suppressing the HGPS mutation may improve symptoms and suggest reversibility.

A 13-year-old boy with a rare genetic condition survived a heart attack and improved with treatment.

A woman with childhood growth hormone deficiency had multiple hormone deficiencies and developed serious lung and kidney problems later in life.

β-catenin helps hair follicle stem cells grow by activating a specific cell pathway.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

The new method is rapid, sensitive, and accurate for evaluating the quality of the medicinal herb Platycladi cacumen.

Hataedock treatment improved skin health and reduced atopic dermatitis symptoms by enhancing the skin barrier and reducing inflammation.

The treatment significantly reduced hair growth and male hormone levels in hirsute women.

Early diagnosis and treatment of NCCAH can improve symptoms and fertility.

PKC ε increases hair follicle stem cell turnover and may raise skin cancer risk.

A gene mutation causes monilethrix in a Chinese family.

Low vitamin C caused bleeding and corkscrew hair, resolved with vitamin C treatment.

CTE can distort results in hair growth trials, so exclude it carefully.

Children with classic congenital adrenal hyperplasia have thicker heart fat and are at higher risk for heart problems and early atherosclerosis.

ECM1-modified stem cells can effectively treat liver cirrhosis.

The man was diagnosed with Cronkhite-Canada syndrome, a rare disorder with GI polyps, skin issues, hair loss, and nail problems.

Removing a methyl group from the ITGAV gene speeds up bone formation in a specific type of bone disease model.

HOXC13 is crucial for regulating hair keratin genes in hair follicles.

DHT may increase the risk of heart disease and death in elderly men.

Genetic testing confirmed a rare disorder causing hair loss and vision problems in a Saudi family, stressing its importance for diagnosis and counseling.

A child with trichothiodystrophy also had autoimmune thyroiditis and anemia, which is a new finding.

The trichohyalin gene is located at chromosomal region 1q21 with other skin-related protein genes.

An infant developed excessive hair growth after a bone marrow transplant and cyclosporine treatment.

Androgenetic alopecia is linked to a higher risk of coronary heart disease due to certain genetic factors and high homocysteine levels.

Trichohyalin is a versatile protein involved in hair and skin structure.

A unique type of complex cyst was found on a man's scrotum.

Mutant CDP/Cux protein causes hair defects and reduced male fertility in mice.