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A man with Woolly Hair Syndrome had very curly, fragile hair, and doctors used a special scalp examination to diagnose him without invasive tests.

Researchers found 617 genes that behave differently in cashmere goat hair follicles, which could help understand hair growth.

The document concludes that systemic therapy is becoming more important in treating head and neck cancer, with new treatments showing promise.

Menopause often leads to lower sexual desire and discomfort during sex, but treatment should be personalized and only if it bothers the woman.

A boy with GAPO syndrome had hair loss similar to male pattern baldness without hormone issues, possibly due to skin or blood vessel problems.

Women with hair loss have higher heart disease risk and unhealthy cholesterol levels.

Pica disorder in central Iraq is mainly found in females and is linked to low iron levels; treatment with iron improves most patients.

Hormonal imbalances are a key cause of missed menstrual periods in women.

Cedrus libani has potential medicinal uses but needs more safety studies.

Antibiotics often cause skin reactions, making them a major health concern.

Tacrolimus causes fewer acute rejections than cyclosporin A in kidney transplants but doesn't necessarily improve kidney function after one year; cardiovascular risks and side effects vary between the two drugs.

Eating well and avoiding synthetic hair products are key for healthy hair.

Women's hair gets thinner and grayer as they age, with treatments available for hair loss and graying.

Aging scalp skin contributes to hair aging and loss, and more research is needed to develop better hair loss treatments.

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.

The study found that a specific genetic variation in the TNFα gene is significantly linked to Alopecia Areata in the Jordanian Arab population.

Rare genetic variants in five specific genes are linked to male-pattern hair loss but only account for a small part of the risk.

The conclusion is that genetic differences affect how the cochlea heals after hair cell loss, which may challenge the creation of hearing loss treatments.

Certain genetic variations in the RAB5B gene are linked to a higher risk of polycystic ovary syndrome in Chinese Han women.

Certain genetic markers can indicate higher or lower risk for systemic lupus erythematosus.

Light-based treatment, Photobiomodulation, shows promise for non-invasive skin therapy with few side effects.

Beard cells, unlike scalp cells, produce growth factors in response to testosterone, which may explain differences in hair growth.

Polycystic Ovary Syndrome (PCOS) is common in women with conditions like anovulation, hirsutism, hair loss, and type 2 diabetes, and it can lead to health risks like heart disease, obesity, insulin resistance, and depression. Non-Classic Congenital Adrenal Hyperplasia (NC-CAH) is also discussed.

The document concludes that stopping shaving or removing affected hair can alleviate Pseudofolliculitis barbae (PFB).

The document concludes that clinicians should be aware of common hair and scalp disorders in women of African descent and that more research is needed to develop effective treatments.

Genetic variants can affect valproic acid's effectiveness, side effects, and levels in epilepsy treatment.

Some women with PCOS have rare genetic variants linked to the condition.

Early hair loss in men could be a sign of non-cancerous prostate enlargement, and treating hair loss early might help prevent prostate issues later.

Fibrodysplasia ossificans progressiva is a rare genetic disorder that causes extra bone growth and symptoms of premature aging.

Personalized treatments for hair loss are becoming more effective by using genetic information.