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A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

Chronic graft-versus-host disease in the skin shows strong Th1 immune response and unique barrier issues.

LSD1 is essential for healthy skin development and creating the skin's protective barrier.

A faulty KLHL24 gene leads to hair loss by damaging hair follicle stem cells.

Mutations in the LIPH gene cause woolly hair in a child.

Minoxidil solution applied twice daily improved hair growth in patients with Woolly Hair/Hypotrichosis due to LIPH gene issues, with mild side effects.

The DLQI is a key tool for measuring quality of life in dermatology.

Discoid lupus patients often have other health issues like systemic lupus, hypertension, depression, and hypothyroidism.

Cadd4 effectively reduces cholesterol levels without side effects.

Mutations in the DSG4 gene cause specific hair and scalp issues.

Patients with hidradenitis suppurativa have higher levels of cell-free DNA in their blood.

Some drugs may cause hair loss in women.

Dermoscopy helps diagnose and monitor treatment for hair loss from scarring conditions like discoid lupus and lichen planopilaris.

High homocysteine levels in lupus may increase inflammation and cardiovascular risk.

Intense pulsed light with radiofrequency showed mixed results in improving quality of life for hidradenitis suppurativa patients, with no clinical improvements.

A girl had two rare hair conditions that helped understand their overlap.

Hairline-lowering surgery effectively reduces a high hairline with immediate, noticeable results.

Hyperaesthetic leucotrichia in horses causes painful, recurring skin lesions and hair color changes, especially in Arabian and American paint horses.

Discoid Lupus Erythematosus often causes scarring hair loss, is influenced by genetics and environment, and requires early treatment to prevent worsening.

The laser therapy device effectively increased hair growth in people with androgenetic alopecia.

High-content screening is useful for finding new treatments for rare diseases and has led to FDA-approved drugs.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

Lack of Vitamin D receptor changes skin structure and increases certain immune cells in the skin.

A woman with lupus and Kikuchi-Fujimoto disease improved with treatment.

The RHD4 gene is crucial for consistent root hair growth in Arabidopsis thaliana.

IL-18 levels are higher in hidradenitis suppurativa patients and may indicate disease severity.

A genetic duplication on chromosome 5 was linked to a woman's unique combination of medical conditions.

The enzyme DHHC13 is essential for healthy hair and skin, and its deficiency leads to hair loss and skin problems.

Psoriasis, acne, and hair loss are linked to unhealthy cholesterol levels, increasing heart disease risk.