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Marie-Unna Hereditary Hypotrichosis is a rare genetic condition causing sparse hair growth, requiring specific recognition for proper care.

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

The document concludes that periocular hair disorders have various causes and treatments, and proper evaluation by specialists is important for management and prognosis.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

Puberty often causes skin issues like acne and excessive sweating, and treatments require patience as results may vary.

Smoking is linked to more hair loss and premature graying compared to nonsmokers.

Minoxidil and finasteride effectively treat hair loss.

Finasteride may effectively treat hair loss in Klinefelter Syndrome patients.

Mutations in the PADI3 gene are linked to a higher risk of scarring hair loss in women of African descent.

The document concludes that treatments like oral anti-androgens, minoxidil, and topical spironolactone can be effective for hair loss in men and women.

Macrophages are more involved in Lichen planopilaris than in Frontal fibrosing alopecia.

Hair, teeth, and mammary glands develop similarly at first but use different genes later.

Cooling the scalp may prevent hair loss from chemotherapy, hair often grows back after treatment, and nail issues usually improve after stopping the drug.

Eating disorders can cause various hair problems, and while hair loss in these disorders is linked to metabolic syndrome, treatment focuses on specific medications and lifestyle changes for the syndrome.

Thyroid diseases may contribute to autoimmune skin diseases, and more research is needed on their relationship.

Dynamic, light touch is sensed through a common mechanism involving Piezo2 channels in sensory axons.

Plant extracts in shampoo improved hair thickness and density in men with hair loss.

Premature graying of hair is often linked with other health issues, but treatment with biotin, zinc, and calcium pantothenate is not very effective.

Homeopathic treatments can effectively manage hair loss and improve well-being.

Skin problems can be caused or worsened by physical forces and pressure on the skin.

A thorough history and examination are crucial for diagnosing skin diseases, which affect up to a third of people. This includes details about skin lesions, medication, general health, lifestyle, family, and contacts, as well as examining the rash, hair, nails, and mucous membranes. Changes in hair and nails can also indicate other medical and skin disorders.

Hair loss is common in autoimmune diseases and can be an early sign of the condition, often requiring prompt treatment to prevent permanent damage.

Pigs without the Hairless gene showed skin and thymus changes, useful for studying human hair disorders.

New hair follicle-targeting treatments show promise for hair disorders but need more research on safety and effectiveness.

Reducing Tyrosinase prevents mature color pigment cells from forming in mouse hair.

The genes KRT25 and SP6 affect curly hair in horses, with KRT25 also causing hair loss. If both genes are mutated, the horse gets curly hair and hair loss. KRT25 can hide the effect of SP6.

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

Understanding how melanocyte stem cells work could lead to new treatments for hair graying and skin pigmentation disorders.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

The cause of Frontal Fibrosing Alopecia is unclear, diagnosis involves clinical evaluation and various treatments exist, but their effectiveness is uncertain.