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A specific gene variation increases the risk of high uric acid and cholesterol in young Mexican males.

Two specific hair keratin genes are active during hair growth and decline as hair transitions to rest.

miR-22 helps skin cancer grow and spread by activating specific cell signals.

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

Longer GGN repeats in the androgen receptor gene are linked to polycystic ovary syndrome.

A new mutation in the STING protein causes a disease with lupus-like symptoms and responds well to a specific inhibitor treatment.

The NIPAL4 mutation c.527C>A is common in Romanian patients with autosomal recessive congenital ichthyosis.

CCCA in women of African ancestry may be caused by PADI3 gene mutations and intense hair grooming.

A gene mutation causes early keratinocyte maturation leading to hair loss in Olmsted syndrome.

A 2-year-old boy with a rare brain malformation may have Gomez–López-Hernández syndrome.

CLEC4D gene variants may increase the risk of alopecia areata in Jordanians.

A specific gene mutation causes woolly hair and hair loss.

A new therapy for a skin blistering condition has not been developed yet.

A new AIRE gene mutation causes rare autoimmune symptoms in a Lebanese boy.

MNC-QQ cell therapy improved hair growth and quality of life in men with androgenic alopecia without adverse effects.

TRPV3 gene mutations cause Olmsted syndrome symptoms, but severity varies.

Overexpressing Dsg3 in mice skin causes excessive cell growth and abnormal skin development.

Certain genetic variations are linked to hair loss in Mexican men.

Specific RNA patterns are linked to alopecia areata.

Certain genetic variants reduce enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

Genetic screening for NUDT15 polymorphisms is crucial for patients taking azathioprine, especially in Asians.

A variant in the ADAM17 gene causes hair loss by increasing protein degradation through TRIM47.

The length of the CAG repeat in the androgen receptor gene affects the risk and progression of prostate cancer, BPH, infertility, and undermasculinized genitalia.

A 21-month-old boy has a rare genetic disorder causing sparse hair due to an LSS gene mutation.

Cupric chloride treatment corrected abnormal Purkinje cell development in brindled mice.

Certain HSD3B1 gene types are linked to worse prostate cancer outcomes and affect treatment response and other health conditions.

A rare gene mutation causes skin fragility and itching without affecting hair or nails.

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.