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Ritlecitinib is being tested for safety and effectiveness in young children with severe alopecia areata.

Targeting the TNFRSF1B gene may help treat hair loss.

A new gene mutation causes vitamin D-resistant rickets and hair loss in two siblings.

KRT14 gene variants cause dermatopathia pigmentosa reticularis, affecting nails, teeth, and hair.

Brg1 is crucial for hair growth and skin repair by maintaining stem cells and promoting regeneration.

Early diagnosis of Trichorhinophalangeal syndrome type 1 is crucial for treatment and was achieved through clinical examination and family history.

A new mutation in the ST14 gene was found in a patient with ARIH syndrome, showing milder symptoms and no tooth issues.

A specific gene mutation causes complete hair loss in an Irish Traveller family.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

A family got a fungal infection from a boy who had contact with rabbits, but they all recovered with treatment.

The gene for Clouston syndrome in a large Indian family is located in the 13q11-q12.1 region.

Ritlecitinib was generally well tolerated in children with alopecia areata.

Haplogroup X found in Altaian population supports Amerindian origin.

Loss of Rap1 protein speeds up heart aging in mice.

AtZP1 protein stops root hair growth in plants by blocking certain genes.

A mutation in the KRT86 gene causes hair fragility in a Turkish family.

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.

Clinicians should consider individual factors and communicate risks and benefits when prescribing ritlecitinib for adolescent alopecia areata.

A variant in the KRT31 gene causes a rare hereditary hair disorder called monilethrix.

A specific gene change is linked to severe hair loss.

Rapp-Hodgkin syndrome, AEC, and EEC are different expressions of the same genetic disorder caused by TP63 gene mutations.

Relatives of lupus patients show signs of immune system activity but not full-blown lupus.

Consider DRIF and perform skin biopsies for persistent papular rashes.

APS-1 in Italy shows diverse AIRE mutations and various autoimmune issues.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

Too much AKR1C3 enzyme causes resistance to finasteride by increasing testosterone.

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

Three siblings with a genetic form of rickets showed different symptoms of the disease.