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A specific gene variant causes severe skin issues and increases infection risk, requiring careful medical monitoring.

Truncating mutations in the C2orf37 gene cause Woodhouse–Sakati syndrome.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

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

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

Genetic differences affect COVID-19 severity and treatment effectiveness.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

Certain genes and high cholesterol levels increase heart disease risk in Ethiopian patients with high blood pressure.

The N363S gene variant does not cause higher adrenal androgen levels in women with polycystic ovary syndrome.

Two new gene mutations cause a rare hair disorder.

The wavy coat in NCT mice is caused by multiple genes, including a mutation in the Prss53 gene.

The ACE1 gene variant doesn't affect long-COVID symptoms.

CTP-543 is generally safe for treating alopecia areata.

Certain gene variations are linked to better memory in healthy Chinese women.

Genetic differences within ethnic groups may affect prostate cancer treatment effectiveness.

A boy's skin fragility and sparse hair were caused by a genetic mutation affecting skin cell adhesion.

Longer TA repeats in the SRD5A2 gene may increase acne risk in Chinese people.

VPS13C variants are linked to more severe REM sleep disorder and faster progression to Parkinson's disease.

There's no significant link between the D19S884 marker at the insulin receptor gene and polycystic ovary syndrome.

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

Specific gene variants affect wool traits in Chinese Tan sheep.

A new ARID1B gene variation causes Coffin-Siris syndrome 1 and early high myopia in a Chinese family.

The method accurately measures cyproterone acetate in plasma, showing no significant difference between two formulations.

HSD3B1 gene variant and being overweight linked to hair loss in women with polycystic ovary syndrome.

Women with greater androgen sensitivity respond better to finasteride for hair loss.

LIPH mutations in Japan cause varying degrees of hair loss and woolly hair.

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

Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

A new gene mutation linked to a skin condition was found in a Spanish family.