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A child has a rare hair and skin disorder due to specific gene variants, suggesting broader genetic testing is needed.

Vitamin D receptor gene changes don't affect alopecia areata risk.

The study concluded that genetic mutations affect human hair diseases and identified key genes and pathways involved in hair growth and cycling.

A young boy's uncombable hair is due to a rare genetic condition that usually improves over time.

A new genetic mutation in mice causes permanent hair loss and skin wrinkling.

Most genetic mutations causing hypohidrotic ectodermal dysplasia in Russian patients are found in the EDA gene.

Certain genes may be linked to autoimmune conditions in people with alopecia areata.

The VDR gene polymorphism does not affect BDNF levels in autoimmune thyroiditis and hypothyroidism patients.

A genetic variant in the KRT25 gene causes tightly curled hair.

The visfatin GT genotype may increase the risk of Alopecia Areata.

No significant link between CAG repeat numbers and female pattern hair loss in Han Chinese population.

Genetic differences may influence male pattern hair loss in Russians.

A 195 bp duplication in the HOXC10 gene causes crests in domestic chickens.

A specific DNA pattern in Malassezia restricta may be linked to hair loss in men.

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

A specific gene region can control targeted and responsive gene expression in mice, useful for skin disorder treatments.

A deletion in the CDH3 gene causes a rare disorder with short hair and vision loss.

BMP receptor IA is essential for proper hair cell differentiation in mice.

BKN-1 antibody targets specific keratin in basal cell epithelioma and normal skin basal cells.

The hepatitis B vaccine did not cause hair loss in the tested mice.

No link found between new male baldness genes and female hair loss.

BTNL2 helps protect hair follicles from immune attacks.

Hair follicle cells resist turning into skin cells.

Mutations in the POC1A gene can cause a unique form of extreme insulin resistance and short stature.

Rare genetic variants in 125 genes are linked to male-pattern hair loss.

A genetic defect causes males in some Mediterranean populations to be born with ambiguous genitalia and develop male traits at puberty.

Human hair keratins were cataloged, showing their roles in hair differentiation stages.

"D-CHRAMPS syndrome" is a newly identified condition with multiple severe symptoms.

Most people have similar hair protein patterns, but a rare variant was found in two women.