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The NUDT15 gene variant causes severe side effects from azathioprine in some Indian patients.

Combining topical delgocitinib with a 308-nm excimer laser can effectively treat severe alopecia areata and vitiligo.

Oral zinc therapy is effective for treating acrodermatitis enteropathica.

A young woman with a rare skin cancer was diagnosed late because her symptoms were unusual for the disease.

CD8+ T cells are involved in alopecia areata and may cause disease relapse.

2-deoxy D-glucose does not help with hair regrowth in alopecia areata.

A child with a rare vitamin D-resistant condition improved with treatment.

A man had bad reactions to a hair loss treatment called DNCB.

A genetic variant in the GJB6 gene likely caused the Labrador's paw pad condition.

A rare gene mutation causes skin fragility and itching without affecting hair or nails.

The Dfl mutation in mice causes poor sebaceous gland function and complete hair loss.

DDR-II hair follicle cells don't respond to 1, 25-dihydroxyvitamin D3, aiding diagnosis.

Skin lesions in Carney Complex are caused by a gene change in some skin cells that leads to increased pigmentation and may lead to tumors.

A woman's hyperandrogenism was caused by a genetic mutation leading to non-classic adrenogenital syndrome.

Some skin conditions are associated with other serious diseases, and office microscopy may miss many fungal infections.

A girl with Denys-Drash syndrome was misdiagnosed due to biotin affecting her hormone test results.

Age-related immune changes significantly affect disease development in other systems.

COVID-19 infection rates were low in patients with immune diseases, regardless of their treatment type.

Biotin deficiency in patients on total parenteral nutrition can cause serious symptoms but can be treated with biotin supplements.

Removing certain hair follicle stem cells worsens skin reactions to allergens.

Certain immune-related proteins are higher in people with alopecia and their healthy relatives, hinting at a genetic link.

Expanding CD4+ Tregs can stop hair loss in alopecia areata.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

Genetic variants in specific genes cause central centrifugal cicatricial alopecia.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

Malondialdehyde-modified DNA may trigger an immune response in alopecia areata patients.

A specific gene mutation causes sparse, brittle hair in a family.

Steroid treatment greatly improved the symptoms of a boy with a rare disorder called Satoyoshi syndrome.

CD90 is abundantly present on stem-like cells in dog hair follicles.

GAPO syndrome causes growth issues, hair loss, missing teeth, and vision problems.