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Researchers found four genes that could help diagnose severe alopecia areata early.

Camellia japonica extract may improve scalp health and promote hair growth.

Wound healing can help prevent hair loss from chemotherapy in young rats by increasing interleukin-1β signaling.

Cronkhite-Canada syndrome can cause multiple gastrointestinal polyps and various physical symptoms.

AB+ blood group is more common in alopecia areata patients.

The Wnt signaling pathway is not a major factor in the development of keratoacanthoma, a type of skin tumor.

Hair loss from Alopecia Areata is caused by both genes and environment, with several treatments available but challenges in cost and relapse remain.

Endocrine diseases in children often cause skin changes like dryness, redness, acne, hair loss, and more.

A family was found with both Trichorhinophalangeal syndrome and Loose Anagen Syndrome, suggesting a genetic connection.

Oral tofacitinib may be an effective and tolerable treatment for some people with severe alopecia areata.

Understanding skin structure and development helps diagnose and treat skin disorders.

A 27-year-old with APS-1 showed improvement in symptoms after treatment.

Ayurvedic herbs can help manage Polycystic Ovarian Syndrome (PCOS).

Non-invasive methods can effectively diagnose and manage alopecia areata.

New research has found 14 genes linked to the risk of developing alopecia areata, improving understanding and treatment options.

Six genetic conditions are often linked to complete scalp hair loss in children.

The report shows a young man with Hutchinson-Gilford Progeria Syndrome had typical and additional eye problems related to the disease.

A young woman had a rare, usually non-cancerous tumor on her face that was initially mistaken for a different condition.

Diphenylcyclopropenone is more effective and has fewer side effects than dinitrochlorobenzene for treating alopecia areata.

Alopecia Areata has no cure, treatments are limited, and the condition often recurs, but new therapies like JAK inhibitors show promise.

A one-year-old child with a genetic condition had symptoms improved by treating zinc deficiency.

Patients with one autoimmune disease should be checked for other autoimmune disorders.

Adjusting the medication tacrolimus resolved a boy's red nail beds after a stem cell transplant.

The conclusion is that the nuclear lamina and LINC complex in skin cells respond to mechanical signals, affecting gene expression and cell differentiation, which is important for skin health and can impact skin diseases.

The nucleus is key in controlling skin growth and repair by coordinating signals, gene regulators, and epigenetic changes.

The document explains various skin conditions and their treatments.

The book explains the science of tissue repair and regeneration, its medical uses, challenges, and ethical concerns.

The document concludes that Syndromes of Severe Insulin Resistance are rare disorders with limited treatment options.

Experts discussed treatments for skin conditions in children, emphasizing hydration, cautious medication use, and early intervention for infections.

Educating patients on phototrichogram increased satisfaction in androgenetic alopecia treatment.