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Scientists successfully grew mini hair follicles using human skin cells, which could help treat baldness.

Disabling the FGF5 gene in sheep leads to longer wool.

Hormones, especially androgens, play a key role in acne, which can be a symptom of systemic diseases like PCOS and may require targeted treatment.

The document concludes that while there are various treatments for Alopecia Areata, there is no cure, and individualized treatment plans are essential due to varying effectiveness.

Genetic testing for cancer risk can lead to early and life-saving treatments in people without symptoms.

CAH is a genetic disorder affecting cortisol production and causing hormonal imbalances, with treatment and diagnosis varying by form and symptoms.

A genetic mutation in the SGK3 gene causes hairlessness in Scottish Deerhounds and may relate to human hair loss.

Pregnancies in a woman with the Donohue mutation were managed with genetic testing, resulting in three healthy infants.

Removing myelin protein zero-like 3 in mice leads to better metabolism and resistance to obesity.

Drug repositioning is becoming more targeted and efficient with new technologies, offering personalized treatment options and growing interest in the field.

Mutation in hairless gene may increase hair loss risk.

Mutation in hairless gene may increase hair loss risk.

Up to 50% of scalp hair can be lost before it appears thin, and treatment is only needed for hair loss caused by diseases or deficiencies.

A thorough initial check-up is essential before sperm banking to ensure the best chance of preserving good quality sperm.

New treatments and diagnostic methods for various animal skin conditions showed promising results.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

New therapies for Birt–Hogg–Dubé syndrome are being developed based on understanding the FLCN gene's role.

Innovative methods are reducing animal testing and improving biomedical research.

LC-MS/MS is more reliable than immunoassays for diagnosing 21-hydroxylase deficiency.

A man with KID syndrome developed a rare cancer in a long-term skin infection.

Male hormones affect COVID-19 severity and certain drugs targeting these hormones could help reduce the risk.

Many people with hair loss had low iron and ferritin levels.

The document concludes that PCOS is a complex disorder caused by both genetic and environmental factors, affecting women's health in various ways, and requires personalized treatment.

Certain genetic variants in the androgen receptor are linked to higher PSA levels, potentially affecting prostate cancer screening outcomes.

A specific gene mutation causes long hair in Angora rabbits.

The document concludes that identifying the cause of amenorrhea is crucial for proper treatment.

Alopecia Areata is linked to a higher risk of several diseases, which vary with age and sex.

People with chronic hives should be tested for thyroid autoimmunity to manage their condition better.

The document concludes that recognizing and properly diagnosing lipodystrophy syndromes is crucial for effective management and treatment.

High-content screening is useful for finding new treatments for rare diseases and has led to FDA-approved drugs.