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Scientists found a new gene in a bacterium that can modify an immunosuppressant drug, potentially helping to treat hair loss.

Patients with certain FoxN1 gene mutations have severe immune issues but normal skin and hair.

Tiger tail banding and hair abnormalities are reliable indicators for diagnosing trichothiodystrophy.

Gene knockout mice developed scars similar to human hypertrophic scars, useful for studying scar progression.

A specific group of early-stage melanocytes is reduced in vitiligo-affected skin, which may explain treatment resistance.

A deficiency in the TTC7A gene causes immune problems, gut issues, and hair loss.

New mutations in hair keratin genes cause the rare hair disorder monilethrix.

Notch signaling is crucial for specifying niche cells in Drosophila testis.

A new genetic change in the keratin 10 gene caused a skin condition called ichthyosis hystrix in a father and his daughter.

Cronkhite-Canada syndrome is a rare disorder needing early recognition and treatment with immunosuppressive therapies and nutritional support to manage symptoms and prevent complications.

Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

A 9-year-old girl has a rare hair disorder causing beaded, sparse hair.

Keratin gene regulation is similar across mammals, affecting hair follicle differentiation.

Activating β-catenin and inactivating PTEN cause follicular tumors, not papillomas, similar to those in Cowden’s Disease.

Clascoterone is a promising topical treatment for hair loss and acne with fewer side effects.

South African sheep breeds have diverse genes affecting traits like coat color, horn development, and wool quality.

Genetic testing can identify causes of rare hair loss disorders in children, but no treatments exist.

The IRF2BP2 gene affects sheep fleece quality by influencing fiber traits.

Skin cells might help spread prion diseases like Creutzfeldt-Jakob disease.

New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

A boy with a rare form of early puberty caused by a new gene mutation responded well to treatment aimed at reducing testosterone and preserving adult height.

New genetic mutations causing hair loss were found in a Chinese family.

Different mutations in the 5 alpha-reductase-2 gene were found in affected individuals in the Dominican Republic, suggesting no common ancestry.

THAP1 gene changes do not affect DYT1 dystonia; finasteride may help reduce tics and OCD in Tourette syndrome.

K6 gene expression can be controlled and manipulated in mice for studying skin disorders.

Hairless mice have longer hair follicles and abnormal structures during the catagen phase.

Clascoterone and minocycline are effective acne treatments with quick results and fewer side effects.

A baby had a unique skin condition with a pale patch and surrounding dark hairs, not linked to other health issues.

The study created a mouse model to mimic degenerative diseases for testing tissue repair and new therapies.