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Some natural ingredients like onion juice, rosemary oil, and pumpkin seed oil may help with hair growth and reducing hair loss.

The Wnt/β-catenin pathway is important for body functions and diseases, and targeting it may treat conditions like cancer, but with safety challenges.

Familial frontal fibrosing alopecia is rare, mostly affects women, and often occurs between sisters or mother-daughter pairs.

Seborrheic dermatitis may contribute to the development of central centrifugal cicatricial alopecia.

The document concludes that skin and nail changes can indicate various underlying health conditions.

The 3D-SeboSkin model effectively simulates Hidradenitis suppurativa and is useful for future research.

The most common skin problems in Indian children are infections and eczemas.

Drugs targeting the JAK/STAT pathway can improve atopic dermatitis but vary in effectiveness for vitiligo and alopecia areata, with generally mild safety concerns.

Uterine leiomyomas don't significantly change gene expression in the scalp of people with Central Centrifugal Cicatricial Alopecia.

Nilotinib can cause keratosis pilaris, a skin condition.

Certain gene variations in PITX2 are linked to a higher risk of male pattern baldness in Indians.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

A boy and his father with hereditary hypotrichosis simplex were treated for hair loss, but the treatment result is unknown.

Researchers found a new genetic mutation causing a rare hair loss condition in the first Japanese child studied.

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

Different hair and scalp disorders cause hair loss or excess hair growth, with various treatments available depending on the specific condition.

Most hair loss disorders can be accurately diagnosed and treated in an outpatient setting.

Bleaching hair damages protein structure, especially keratin, leading to weakened hair.

Hair microscopy is useful for diagnosing certain hair loss conditions but has limitations and must be interpreted carefully.

Mutant mice help researchers understand hair growth and related genetic factors.

Female pattern hair loss has unclear causes, possibly involving genetics, hormones, and environment, and needs better treatments.

The document concludes that early diagnosis and treatment are crucial for managing rare hair loss disorders and that more research is needed to improve treatment strategies.

Lichen Planopilaris and Frontal Fibrosing Alopecia may help us understand hair follicle stem cell disorders and suggest new treatments.

Children's hair grows in different types from before birth through puberty, with growth rates and characteristics varying by age, sex, and race.

The document concludes that an experimental drug may help wound healing in Epidermolysis Bullosa, links Hydroa vacciniforme to EBV, discusses diagnosing hair loss disorders, finds many children with eczema have allergies, reviews the safety of a skin medication in children, notes side effects of a Duchenne's treatment, and identifies a marker for pediatric mastocytosis.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

Oral minoxidil shows promise in treating monilethrix-related hair loss.