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People living with HIV in Turkey often have skin conditions, which are more common in advanced HIV stages and may help in diagnosing the infection.

A genetic mutation in the LIPH gene causes a rare hair disorder with sparse, curly hair.

Early-onset hair loss is linked to Parkinson's disease and decreased fertility.

Skin cells can naturally limit the growth of cancerous changes by balancing cell renewal and differentiation.

Blocking certain pathways with kinase inhibitors may help treat cutaneous lupus erythematosus.

PRDX5 enzyme may contribute to alopecia areata by affecting oxidative stress and autoimmunity.

The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

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

The first Japanese case of a genetic hair disorder caused by specific mutations in the LIPH gene was identified.

The balance between cell renewal and differentiation controls the growth of cancerous cells in mouse skin.

A genetic hair protein variant is more common in Japanese people and is inherited.

A specific gene mutation causes a rare hair loss condition in a Chinese patient.

Researchers found a new genetic mutation causing a rare hair loss condition in the first Japanese child studied.

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

RSPO1 mutations in certain patients lead to skin cells that don't develop properly and are more likely to become invasive, increasing the risk of skin cancer.

A woman's long-term scalp issues were diagnosed as a rare skin disorder called cutaneous Langerhans cell histiocytosis.

High lactate dehydrogenase activity is not necessary for the growth of squamous cell carcinoma.

A rare gene variant causes hair and nail issues in a family.

Mutations in the PADI3 gene may cause central centrifugal cicatricial alopecia in women of African ancestry.

A specific gene variant is linked to severe insulin resistance and hormone imbalance in a teenage girl.

Seven new genetic risk areas for prostate cancer were found.

The ND1 gene of the Asian black bear Sichuan subspecies is similar to other bear species.

The research linked PLCD1 gene variants to the development of trichilemmal cysts.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

A new mutation in the HJV gene was found in a young woman with juvenile hemochromatosis, causing unusual symptoms like secondary hypothyroidism.

The study suggests that analyzing DNA can help treat hair loss, but more research is needed.

Mutations in the PADI3 gene are linked to a higher risk of scarring hair loss in women of African descent.

A certain gene variant may increase the risk of polycystic ovary syndrome in Chinese women.

Sweet syndrome can be the only sign of hairy cell leukemia relapse.