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A rare skin condition was confirmed to be associated with a specific virus in a young girl.

Recent progress has been made in understanding inherited hair and nail disorders.

Sex hormones like estrogen and testosterone may affect COVID-19 severity differently in men and women, potentially influencing prevention and treatment strategies.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

Cronkhite-Canada syndrome is a rare, non-inherited condition causing various symptoms like polyps, hair loss, and weight loss.

People with the same genetic mutation for Woodhouse-Sakati syndrome can have different symptoms.

Different types of persistent hair loss after chemotherapy respond differently to treatments.

New regenerative treatments for hair loss show promise but need more research for confirmation.

Rituximab may be an effective treatment for Cronkhite-Canada syndrome with kidney disease.

Dermoscopy and trichoscopy are useful for diagnosing skin signs in Dermatomyositis.

Early treatment of Lupus Erythematosus Alopecia can prevent permanent hair loss, and various medications are effective.

Congenital triangular alopecia is a hair loss condition present from birth or early childhood with no effective treatment needed.

People with Epidermolysis bullosa have many health problems including poor oral health, which is often neglected due to other medical issues.

Early hormones shape sex-specific differences in rat glands.

Treatment with methotrexate and prednisolone led to complete hair regrowth and no relapse for 2 years.

Tofacitinib helped a woman regrow her hair without relapses after other treatments failed.

Using animal names for skin conditions helps with learning and memory.

A man with total hair loss developed blackhead-like spots on his scalp, possibly because no hair was present to help drain oils.

New treatments for alopecia areata show promise, but standardized guidelines are needed.

A 5-year-old boy was diagnosed with congenital triangular alopecia, a type of hair loss without skin changes, usually starting between ages 2-5, with no specific treatment.

People with Down syndrome are more likely to experience hair loss, and using dermoscopy can help diagnose it.

Fibroblasts are crucial for tissue repair and inflammation, and understanding them can help treat fibrotic diseases.

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

Cantú syndrome is caused by mutations in the ABCC9 gene.

Hair follicles are normally protected from the immune system, but when this protection fails, it can cause hair loss in alopecia areata.

Mutations in the RBPJ gene cause Adams-Oliver Syndrome.

Chemotherapy damages hair follicles, causing hair loss and other cellular changes.

The conclusion is that genetic testing is important for diagnosing and treating various genetic hair disorders.

Scalp cooling can help prevent hair loss from chemotherapy, but treatment should be tailored to the individual and more research is needed.

Trichoscopy can help diagnose and monitor the progression of dissecting cellulitis.