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Genes related to keratin, skin cell differentiation, and immune functions are key in hedgehog skin and spine development.

The study found that certain genes are important for hedgehog skin appendage development and immunity, with spines possibly evolving for protection and infection resistance.

Basonuclin 2 is vital for the development of facial bones, hair follicles, and male germ cells in adult mice, and its absence can lead to dwarfism and abnormal follicles.

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

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

Different ectodermal organs like hair and feathers regenerate differently, with specific stem cells and signals involved in their growth and response to the environment.

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

A patient with Cronkhite-Canada Syndrome developed colon cancer that spread to the liver, showing the need for regular cancer checks in such patients.

Topical drugs and near-infrared light therapy show potential for treating alopecia.

Diagnosing alopecia areata is challenging and requires careful examination and various tests to distinguish it from other hair loss types.

There is no standard treatment for the rare Cronkhite–Canada syndrome, which can be fatal and lead to cancer.

Foxn1 gene regulation is crucial for thymus development but not for hair growth.

Sodium hypochlorite can effectively prevent and remove Staphylococcus aureus biofilms in atopic dermatitis at high enough concentrations.

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.

Mice without certain skin proteins had abnormal skin and hair development.

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

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

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

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

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

New treatments for immune disorders caused by FOXN1 deficiency are promising.

A patient with Cronkhite-Canada syndrome improved with nutritional support and steroids, but early diagnosis is key due to high mortality.

Ruxolitinib significantly improves multiple autoimmune conditions in APS-1 patients.

A rare genetic mutation found in an Indian family can be detected through prenatal screening.

A 78-year-old man with Cronkhite-Canada syndrome improved significantly after treatment and remains symptom-free.

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

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

Follistatin helps hair growth and cycling, while activin prevents it.

Researchers found a way to create cells from stem cells that act like human cells important for hair growth and could be used for hair regeneration treatments.

Gene network oscillations inside hair stem cells are key for hair growth regulation and could help treat hair loss.