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

Alopecia areata is an autoimmune disease causing patchy hair loss, often with other autoimmune disorders, but its exact causes are unknown.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

The study found genetic differences related to hair development that may explain hair loss in a patient with Trichorhinophalangeal syndrome type I.

Certain natural and synthetic compounds may help treat inflammatory skin diseases by targeting a specific signaling pathway.

Acne is a common skin condition linked to diet, hormones, and genetics, and early treatment can prevent scarring.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

CYLD mutations cause a variety of skin tumors with symptoms starting around age 16, and treatments are currently limited.

There are many treatments for permanent hair loss disorders, but their effectiveness varies and there's no clear best option.

The document concludes that different types of permanent hair loss conditions are related and early treatment is key to preventing further damage.

Researchers found a new early sign of Frontal Fibrosing Alopecia that could help avoid misdiagnosis.

Melanocytes produce melanin; their defects cause vitiligo and hair graying, with treatments available for vitiligo.

New treatments and early diagnosis methods for permanent hair loss due to scar tissue are important for managing its psychological effects.

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.

Bald thigh syndrome in sighthounds is caused by structural defects in hair shafts due to downregulated genes and proteins.

Lack of cystatin M/E causes thin hair and dry skin.

Frontal Fibrosing Alopecia is a type of hair loss affecting mostly older women, with no agreed best treatment.

The document reports unique growth lines in a child after Stevens-Johnson syndrome, skin reaction from parsnips and sun in a girl, and itchy skin with xanthomas in a boy with Alagille syndrome.

Nerves are crucial for the regeneration of various body parts in many animals.

Afro-textured hair is more fragile and prone to certain scalp conditions, requiring careful treatment and more research for effective management.

Cannabinoids like CBD and THC may help treat non-cancer skin diseases, but more research is needed.

The UD-PrOZA program successfully diagnosed 18% of adult patients with rare diseases, often using genetic testing.

Hair gets thinner, grayer, and changes texture with age due to genetics, environment, and cellular changes, affecting the growth cycle.

Genetic mutations can cause hair growth disorders by affecting key genes and signaling pathways.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

We need better treatments for hair loss, and while test-tube methods are helpful, they can't fully replace animal tests for evaluating new hair growth treatments.

Hair growth serums A and C can affect hair growth genes and pathways, suggesting potential for personalized hair loss treatments.

Certain fungi protect skin health, but changes can allow harmful fungi to cause serious infections, needing more research for treatment and control.

Gastric bypass surgery improved a woman's hormonal disorder without the need for medication.

Asia has made significant progress in tissue engineering and regenerative medicine, but wider clinical use requires more development.