Search

everythinglearnresearchcommunity

for

Search:↓

Loose anagen hair syndrome in children often resolves on its own.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

The document concludes that reactivation of herpesviruses, especially HHV-6, is linked to severe symptoms and complications in drug-induced hypersensitivity syndrome.

Lhx2 is essential for effective Sonic Hedgehog signaling in early retinal development.

Hyperaesthetic leucotrichia in horses causes painful, recurring skin lesions and hair color changes, especially in Arabian and American paint horses.

Two siblings with a genetic mutation had a form of rickets that doesn't respond to vitamin D.

A multidisciplinary approach is crucial for managing Silver-Russell syndrome effectively.

Er:YAG laser therapy effectively treats Hailey-Hailey disease, leading to long-term remission and improved quality of life.

The Foxn1 gene mutation causes hairlessness and immune system issues, and understanding it could lead to hair growth disorder treatments.

Mutant mice help researchers understand hair growth and related genetic factors.

Young Czech women with PCOS have a higher risk of heart problems and should be regularly checked for cholesterol and glucose issues.

Melatonin affects mouse skin and may regulate skin functions.

Testosterone replacement may improve sexual desire and bone health in women with low androgen levels, but more research is needed on its long-term safety.

Current and future treatments for alopecia areata focus on immunosuppression, immunomodulation, and protecting hair follicles.

ROR2 is essential for hair follicle stem cell renewal and maintenance.

Finasteride affects brain processes related to neurotransmission and metabolism, potentially helping with neuropsychiatric conditions.

A man with rare Lichen Planopilaris lost body hair, not scalp hair, and treatment stopped itching but didn't regrow hair.

Researchers found stem cells in dog hair follicles using specific markers.

Spin traps like PBN could protect skin from pollution and sunlight in cosmetics but need more research for safe use.

Herpes gestationis is linked to certain antigens, atopic eczema affects T cell populations and may be eased by breastfeeding, higher doses of anti-androgen treatment can improve androgenic alopecia, topical minoxidil increases hair thickness, long-term methotrexate therapy can cause liver fibrosis in psoriasis patients, and Lichen Sclerosus et Atrophicus patients aren't at higher risk for autoimmune disorders.

A genetic mutation in the CDH3 gene causes hair loss and vision problems in a young Saudi girl.

A genetic variant in the KRT71 gene may cause loose anagen hair and wooly hair, and symptoms might improve with age.

Lichen spinulosus, usually seen in young people, can rarely occur in adults, as shown by a 52-year-old woman with a rough, bumpy rash.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

Laser hair removal effectively reduces hidradenitis suppurativa symptoms with few side effects.

A rare gene variant causes sexual development issues in siblings, needing personalized treatment.

The LMNA mutation affects skin structure even in asymptomatic carriers.

A Chinese family had a child with a specific gene mutation causing vitamin D-resistant rickets, but the child improved with calcium and low-dose calcitriol.

A gene deletion in DSG4 causes sparse hair in some Pakistani families.