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Four genetic risk spots found for hair loss, with WNT signaling involved and a link to curly hair.

New genes and pathways are important for testosterone production and male sexual development.

Dermatoscopy is a useful tool for diagnosing hair disorders and can help choose samples for more detailed analysis.

The document concludes that careful evaluation is key to diagnose and treat women with hair loss, with tests for thyroid, iron, and hormones as needed.

The article explains the genetic causes and symptoms of various hair disorders and highlights the need for more research to find treatments.

Men with enlarged prostates often have more severe baldness.

Regenerative pharmacology, which combines drugs with regenerative medicine, shows promise for repairing damaged body parts and needs more interdisciplinary research.

The LRRK2-G2019S mutation in Parkinson's disease has a lifetime penetrance of 25-35%, and finasteride may help reduce symptoms in adult male Tourette syndrome patients.

Finasteride reduces Tourette syndrome symptoms, but results may be limited due to potential biases.

To diagnose Polycystic Ovarian Syndrome, two out of three signs—irregular periods, high male hormone levels, or cysts on the ovaries—are needed.

Female pattern hair loss has unclear causes, possibly involving genetics, hormones, and environment, and needs better treatments.

Genetic mutations can cause hair growth disorders by affecting key genes and signaling pathways.

Early and personalized treatment for hair loss in young people is crucial to prevent permanent damage and should include psychological support.

Finasteride may help reduce symptoms in male Tourette syndrome patients.

Using steroids can increase the risk of heart problems.

Adrenal disorders can cause lasting brain and behavior issues in children.

Accurate clinical, histological, and genetic methods are key for understanding and treating hair disorders.

Ectodermal dysplasia causes various symptoms and early treatment is important for eye, dental, and skin issues.

Losing eyelashes or eyebrows can be a sign of many different health problems and needs a careful approach to treat effectively.

Mice are useful for researching human hair loss and testing treatments, despite some differences between species.

Androgens like testosterone are important hormones for both men and women, made differently in each sex and affecting the body by regulating genes and quick interactions with cell components.

Some congenital hair disorders improve in childhood or with treatments like minoxidil and retinoids, while others like Netherton syndrome and trichothiodystrophy have a poor prognosis.

The document describes a woman with familial Parkinson's disease due to a genetic mutation, showing severe symptoms and poor response to treatment, and suggests finasteride may help reduce symptoms in Tourette syndrome.

The document concludes that early diagnosis and treatment are crucial for children with hair loss to prevent permanent damage, although not all conditions can be effectively treated.

Most hair loss in children is caused by a few common conditions, and it's important to diagnose these properly and support the child's mental health.

Acne is significantly influenced by genetics, and understanding its genetic basis could lead to better, targeted treatments.

Light microscopy is useful for diagnosing different hair disorders.

Diabetes often causes various skin problems and complications.

The meeting focused on understanding, diagnosing, and finding treatments for irreversible hair loss diseases.

Bimatoprost can cause longer, thicker, darker eyelashes and eyebrows.