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Carriers of a specific gene mutation have subtle skin changes without visible symptoms.

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

A gene mutation in mice causes permanent hair loss and skin issues.

CARASIL can cause different symptoms even with the same genetic mutation.

A rare genetic mutation causes Woodhouse-Sakati syndrome symptoms.

Ptprq has multiple forms that change during inner ear development.

CD8A and FOXD2-AS1 may be key for diagnosing and treating alopecia areata.

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

Mutations in the DSG4 gene cause a severe form of brittle hair and skin issues.

The MLPH gene is not linked to seasonal hair loss in Rhodesian Ridgeback dogs.

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

A gene called HDAC9 might be a new factor in male-pattern baldness.

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

A mutation in the IKZF1 gene causes immune system overactivity, linked to autoimmune diseases like lupus.

Black hairy tongue can be an early sign of graft-versus-host disease after stem cell transplants.

A genetic defect in an Appenzeller Mountain Dog caused skin issues, improved with ketoconazole, showing the importance of advanced genetic testing.

A mutation in the hairless gene speeds up severe itchy skin in mice on a special diet.

The new antibody, TYHF-1, specifically targets certain hair-related structures.

The human type II 5α-reductase gene, linked to certain male health conditions, has a specific structure and low similarity to other related genes.

Genetic testing can diagnose hair loss linked to DSG4 gene variants.

NKG2D+CD4+ T cells are higher in alopecia areata patients and may be involved in the disease.

A new gene mutation causes vitamin D resistance and hair loss in two unrelated girls.

A new patch can deliver stable antibodies over time for potential HIV treatment.

Farudodstat can prevent hair follicle immune damage linked to alopecia areata.

Genomic profiling for myeloid cancers can find important inherited mutations, but it's challenging when these mutations aren't related to the patient's symptoms.

A specific gene mutation causes hair loss and potential eye issues, even if vision seems normal.

Selective breeding can enhance immunity in dairy cattle.

A new genetic mutation in the hairless gene causes a rare hair loss disorder.

ULBP3 could be a marker for diagnosing alopecia areata incognita and may be linked to its cause and development.

Crash dieting can cause hair loss due to severe calorie restriction.