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Certain gene variations increase the risk of alopecia areata in Koreans.

This text talks about how to treat hair loss in women. It suggests different options and stresses the importance of support.

The document concludes that parathyroid diseases have a range of clinical features and outcomes, with some conditions being treatable and others having a high risk of mortality.

Cantu syndrome, which causes excessive hair growth and skin issues, is due to a mutation in the ABCC9 gene, and understanding this could help develop new treatments for hair diseases.

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

The document concludes that various childhood hair and nail disorders exist, some may improve on their own, and advances in genetics and immunology could enhance treatment and counseling.

COVID-19 may worsen with androgens; anti-androgen drugs could help.

Researchers found a new genetic mutation causing a rare hair loss condition in the first Japanese child studied.

The document reports three sisters with Woodhouse-Sakati syndrome showing typical symptoms and unusual gynecological anomalies.

Topical cetirizine 1% promotes hair growth in male androgenetic alopecia patients.

Recognizing congenital triangular alopecia is crucial to avoid unnecessary treatments.

An 11-year-old girl with a rare skin disorder also had cornea issues and dry eye, needing careful management.

The document concludes that a thorough history, physical exam, and specific tests are crucial for diagnosing and managing hair loss effectively.

A woman had 13 non-cancerous cysts on her scalp successfully removed in one surgery.

Oral zinc therapy is effective for treating acrodermatitis enteropathica.

Male pattern baldness is often genetic and linked to a hormone, with treatments like finasteride and minoxidil being effective for some men.

Using cetirizine on the skin and taking vitamin D can help increase hair growth in children with hair loss from ectodermal dysplasia.

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

Using minoxidil and tretinoin on the skin, along with oral vitamin D, improved hair thickness and density in two girls with woolly hair.

A man's baldness improved possibly due to a medication that blocks male hormones.

Ayurvedic treatment helped reduce PCOS symptoms in a 19-year-old girl.

Baldness may lower the risk of testicular cancer.

Hutchinson-Gilford Progeria Syndrome is a rare genetic disorder caused by a specific gene mutation, characterized by aging symptoms and managed by monitoring heart health and using low-dose aspirin.

Acne is a common skin condition linked to diet, hormones, and genetics, and early treatment can prevent scarring.

Finasteride 1mg daily effectively increases hair growth and slows hair loss in men with male pattern baldness over two years.

Red and infrared light therapy improves hair growth in balding patients.

Early detection and multidisciplinary treatment are crucial for managing Papillon-Lefévre syndrome.

Hair loss is linked to heart disease and metabolic syndrome, and while current treatments vary in effectiveness, more research is needed for better solutions.

A teenager's hair with alternating white and dark bands, known as Pili annulati, is a genetic condition that is usually harmless and often considered attractive.