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The TRPV3 gene variant may cause the long-haired suri alpaca coat.

The review shows that skin symptoms like chronic fungal infections, hair loss, and skin depigmentation are key for early detection and management of APECED.

Bioassays help find useful compounds in nature for making medicines, supplements, and cosmetics.

The hair growth serum Trichosera® was effective in increasing hair regrowth and density and reducing hair fall without significant side effects.

ILC1-like cells can independently cause alopecia areata by affecting hair follicles.

The document concludes that managing Dunnigan-Type Familial Partial Lipodystrophy involves treating associated health issues and using medications like metformin and leptin replacement.

The 2015 Hair Research Congress concluded that stem cells, maraviroc, and simvastatin could potentially treat Alopecia Areata, topical minoxidil, finasteride, and steroids could treat Frontal Fibrosing Alopecia, and PTGDR2 antagonists could also treat alopecia. They also found that low-level light therapy could help with hair loss, a robotic device could assist in hair extraction, and nutrition could aid hair growth. They suggested that Alopecia Areata is an inflammatory disorder, not a single disease, indicating a need for personalized treatments.

The UK's EDS National Diagnostic Service found that early diagnosis, lifestyle advice, and regular check-ups are crucial for managing vascular Ehlers-Danlos syndrome. A combination of losartan and bisoprolol can reduce vascular events, improving survival and quality of life.

Low oxygen levels improve the function of hair and skin cells when they are in direct contact.

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

Genetic variations greatly affect individual metabolism and can impact health and disease risk.

Blue light might help treat skin conditions by affecting the skin's bacteria.

Different types of atopic dermatitis were linked to specific genetic and immune changes, suggesting that severe cases might need stronger immune-targeting treatments.

Indian women with PCOS from Delhi and Srinagar show different symptoms, with Delhi women having higher obesity and blood sugar issues, and Srinagar women showing more hair growth and testosterone levels.

The specific skin disease variant p.(Arg2000Trp) in plectin can cause a wide range of symptoms, which should be considered when diagnosing patients.

The study found that in Latin America, ancestry varies by location, influences physical traits, and affects how people perceive their own heritage.

The current methods for diagnosing polycystic ovary syndrome are too vague and may lead to misdiagnosis and problems in research.

Some parents have a mild form of congenital adrenal hyperplasia without symptoms, and they usually don't need treatment.

Caucasian and Asian women with PCOS generally show similar symptoms, except Asian women have less chest hair.

WNT10A mutations cause varied symptoms in patients with odonto-onycho-dermal dysplasia.

Women with PCOS should be screened for heart disease risk and manage their health to prevent it.

DHT's role in hair loss is important, but measuring its level for diagnosis is questionable.

Measuring the distance from the anus to the clitoris may moderately help diagnose polycystic ovary syndrome, especially in certain cases.

PCOS is linked to low-grade chronic inflammation.

Polycystic ovary syndrome affects about 6-10% of women, with varying symptoms and the need for standardized global definitions.

Different hair fiber development might explain why hair loss severity varies in patients with a specific genetic mutation, and treatments that thicken hair could help.

Two specific SNPs in the TRPS1 gene cause excessive hair growth by altering the protein's structure.

Patients with both connective tissue disease and acid reflux are more likely to have certain symptoms and physical signs.

MendelVar is a tool that helps identify important genes by combining GWAS data with Mendelian disease information.

Combining genetic and physical trait analysis improves diagnosis accuracy for monogenic diabetes.