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Melatonin may help with nerve pain, a hepatitis C drug is effective but has side effects, a treatment for mouth sores works but can cause blood issues, ear reconstruction with an implant is safe, HIV transmission from mother to child in Taiwan is now 0% with treatment, certain blood problems are more common in people with a tongue condition, a gene and being overweight are linked to hair loss in some women, a new technique could reduce radiation for lung nodule patients, a hepatitis treatment may lower cancer recurrence after a procedure, and adding extra screening improves tuberculosis detection in patients with lung infections.

Gene variations may increase oxidative stress in male pattern baldness.

SRD5A2 gene variations affect PTSD symptoms differently in males and females.

A unique gene mutation causes vitamin D-resistant rickets without causing hair loss.

New gene discoveries have improved diagnosis and treatment for skin and hair disorders, but more research is needed to fully understand them.

Genetic mutations linked to ectodermal dysplasias and hair loss were identified in Pakistani families.

A rare genetic variant linked to skin cysts was found in blood DNA, suggesting its role in cyst formation.

Alopecia areata involves specific immune cells, offering potential treatment targets.

A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

Machine learning improves DNA predictions for eye and hair color, but challenges remain for skin tone and facial features.

A gene mutation in Lama3 is linked to a common type of hair loss.

Rare genetic variants contribute to male pattern hair loss, but there's no link to severe COVID-19.

Certain immune cells are linked to non-scarring hair loss, suggesting potential for immune-targeted treatments.

Monilethrix is linked to a gene cluster on chromosome 12.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

A specific gene mutation causes vitamin D-resistant rickets and hair loss.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

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

Certain RNAs may help diagnose alopecia areata by affecting keratin genes.

Hidradenitis suppurativa may be more severe in people with Mediterranean fever gene mutations.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

Alopecia areata is a common autoimmune disease affecting hair follicles, with unclear causes and a need for better treatments.

Lgr5 and the vitamin D receptor are key in controlling skin inflammation and tumor risk in mice.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

The HtrA1L364P mutation causes brain dysfunction and blood vessel damage.

New LSS gene variants help understand congenital hypotrichosis 14 better.

Certain gene variations might be linked to severe acne in women but not in men.

The gene for Marie Unna hereditary hypotrichosis is located on chromosome 8p21, near the hairless gene.

The PML protein helps prevent skin cancer in mice.

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