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The review shows that skin symptoms like chronic fungal infections, hair loss, and skin depigmentation are key for early detection and management of APECED.

AIRE-deficient rats developed severe autoimmune disease similar to APECED, useful for testing treatments.

Ichthyosis with confetti is a genetic skin disorder with consistent ectodermal malformations and various KRT10 gene mutations.

Neonatal hair can help determine drug exposure during pregnancy.

Human sweat glands have a type of stem cell that can grow well and turn into different cell types.

Platelet-rich plasma (PRP) is a simple, cost-effective treatment that promotes hair growth and reduces hair loss, with high patient satisfaction.

Cronkhite-Canada Syndrome often leads to death within 6-18 months.

The conclusion is that skin and hair patterns are formed by a mix of cell activities, molecular signals, and environmental factors.

Monilethrix Syndrome causes fragile, beaded hair that breaks easily and needs early diagnosis for better care.

A new mutation in the K6b gene caused a girl's late-appearing nail condition.

The article concludes that studying how skin forms is key to understanding skin diseases and improving regenerative medicine.

Hair loss in Cronkhite-Canada syndrome may be due to an autoimmune response.

Removing Mediator 1 causes teeth cells to turn into hair cells.

A Laotian man with unusual skin changes and multiple growths in his gut was diagnosed with Cronkhite-Canada Syndrome and improved with nutritional and immune-based treatments.

An 11-year-old child with total hair loss may have a genetic autoimmune disease, and the outlook for hair regrowth is not good.

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

Albumin and prednisone improved symptoms in a woman with Cronkhite-Canada syndrome, revealing potential genetic causes.

Cronkhite-Canada syndrome is rare, has a poor prognosis, and requires early diagnosis and ongoing treatment.

Prednisone treatment helped a woman with Cronkhite-Canada syndrome recover from hair loss and digestive issues.

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

Stem cells in hair follicles can become various cell types, including neurons.

Skin biopsy is crucial for diagnosing unknown baldness causes.

Blocking a specific protein signal can make hair grow on mouse nipples.

GFP transgenic mice help study cell origins in skin grafts.

Alopecia areata causes varying hair loss patterns, affecting hair, nails, and possibly glands, with treatment outcomes depending on disease duration and extent.

Most orthodontic patients with missing teeth also have hair disorders.

The skin is vital for protection, temperature control, fluid balance, immunity, and sensing, with damage affecting daily life and mental health.

ATP-dependent chromatin remodeling is crucial for skin development and stem cell function.

Scientists turned rat thymus cells into stem cells that can help repair skin and hair.

Msx2 and Foxn1 are both crucial for hair growth and health.