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

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

Human adrenals and gonads have a unique enzyme for steroid hormone production.

A new genetic mutation was found causing hair and eye issues in a boy.

A specific gene change in APCDD1 increases the risk of hair loss.

The document concludes that certain mutations may contribute to the inflammation in hidradenitis suppurativa and suggests that targeting TNFα could be a treatment strategy.

The androgen receptor gene doesn't affect women with recurrent spontaneous abortions, but having a mutant genotype might protect against it.

Certain gene variations and different levels of BDNF and CRH hormones are linked to vitiligo.

Certain genetic variants are linked to frontal fibrosing alopecia in Spanish patients.

Certain gene variations increase male hair loss risk, influenced by hormone levels.

The hr gene is linked to hair loss in Valle del Belice sheep.

Certain genetic markers on chromosome 20 are linked to hair loss in the Han Chinese from Yunnan.

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

A new DSG4 gene mutation causes hair defects in a young girl.

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

People who carry the 21-Hydroxylase Deficiency gene are not more likely to have excessive male hormone levels.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

Targeting IL-15 may help treat Alopecia Areata.

HOXC13 is essential for hair and nail development by regulating Foxn1.

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

A mutation in the VDR gene affects hair cycling without needing ligand binding.

The Thr1022Ala variant in the hairless gene is not a disease-causing mutation.

A new mutation in the hHb1 keratin gene is linked to the hair disorder monilethrix.

WNT10A mutations cause varied symptoms in patients with odonto-onycho-dermal dysplasia.

The Tru9I variant in the VDR gene may influence alopecia areata risk and vitamin D levels.

Certain genetic markers may increase or decrease prostate cancer risk.

The HOXC13 gene affects different hair proteins in cashmere goats in varied ways and is controlled by a feedback loop and other factors.

5% topical minoxidil improves hair density and quality in monilethrix patients.

Certain variations of the HDAC9 gene can increase or decrease stroke risk in the Chinese population.

A mutation in the hHb3 gene is linked to the hair disorder monilethrix.