Search

everythinglearnresearchcommunity

for

Search:↓

Human skin has multiple layers and functions, with key roles in protection, temperature control, and appearance.

Men with early balding should be checked for metabolic syndrome, as there's a link between the two.

Alopecia in animals can be hereditary, congenital, or acquired, with treatments and outcomes varying widely.

UK medical students lack dermatology education, liver biopsy patients with risk factors show more fibrosis, and certain fungi resist drugs due to melanin; genetics may influence female hair loss.

The document suggests a bacteria plays a significant role in acne rosacea and that white hair can regain color after transplant, meriting more research on reversing grey hair.

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.

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

Cats with abnormal hair had DSG4 gene changes causing hair problems.

Alopecia in patients with epidermolysis bullosa varies in severity and is often caused by skin blistering or trauma.

An 87-year-old woman was diagnosed with type 3 autoimmune polyendocrine syndrome and had multiple autoimmune issues.

Low-dose acitretin helps nail psoriasis, stem cells may treat scarring alopecia, Chinese men have lower baldness rates, lateral foldplasty is good for ingrown toenails, hair diameter helps diagnose female baldness, childhood trauma linked to alopecia areata, certain hair-weaving leads to scalp conditions in African American women, and new methods for hair research and understanding hair and sweat gland development were introduced.

Nagashima-type palmoplantar keratosis in Asians is caused by a SERPINB7 gene mutation.

Mice with extra human KLK14 had hair and skin problems, including weaker cell bonds and inflammation, linked to Netherton syndrome.

Middle Eastern patients with epidermolysis bullosa show specific genetic mutations linked to different types of the disease.

Autoimmune polyglandular syndrome can cause temporary brain issues that may improve on their own.

Oral retinoic acid effectively treated collodion baby, with hair loss as the main side effect.

Netherton syndrome can cause severe and chronic vulvovaginal symptoms that may improve with continuous oral contraceptives.

Tofacitinib helps regrow hair in severe alopecia patients, but more research is needed.

Baricitinib reduces inflammation and improves cell health in premature aging cells.

Cyclosporine-A can cause excessive hair growth, which usually stops after discontinuing the drug.

FGF5 gene mutations cause unusually long eyelashes by affecting hair growth regulation.

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

Knocking out certain genes in mice helps understand skin and hair growth problems.

Matriptase is highly active in hair follicles and sebaceous glands, especially during hair growth phases.

Sudden, unusual hair loss may indicate serious underlying health issues.

A woman with lupus had muscle weakness due to kidney issues and was successfully treated with medication.

In India, most patients with type 1 autoimmune polyglandular failure show symptoms in a specific order, starting with parathyroid gland issues, then yeast infections, and finally adrenal gland failure.

Netherton's syndrome is linked to high IgE levels and unique skin and hair symptoms, and may improve with ammonium lactate lotion and allergy management.

A boy's skin fragility and sparse hair were caused by a genetic mutation affecting skin cell adhesion.