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The length of the CAG repeat in the androgen receptor gene affects the risk and progression of prostate cancer, BPH, infertility, and undermasculinized genitalia.

Recognizing oral symptoms can help diagnose and treat blood and nutritional diseases early.

There's no significant link between the D19S884 marker at the insulin receptor gene and polycystic ovary syndrome.

Kennedy's disease leads to muscle weakness without a cure, but exercise and managing symptoms may help patients live a normal lifespan.

Low-potency steroids can cause serious side effects in people with skin conditions like Netherton syndrome.

Cells from a skin condition can create new hair follicles and similar growths in mice, and a specific treatment can reduce these effects.

Marie Antoinette syndrome causes sudden hair whitening, but its exact cause is unknown.

Nonclassic congenital adrenal hyperplasia is a genetic disorder causing hormone imbalances, affecting fertility and requiring personalized treatment.

Testing for CAG repeat polymorphism in the androgen receptor gene is not currently recommended for managing hypogonadism.

With careful management, people with congenital adrenal hyperplasia can have successful pregnancies and become parents.

Rapamycin treatment helps with mitochondrial disease by reducing PKC levels.

The Androgen Receptor could be a target for treating diseases like cancer, but more research is needed to confirm the effectiveness of potential treatments.

Genetic mutation and carcinogen treatment are both needed for skin cancer to develop in these specific mice.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

Mutation in hairless gene may increase hair loss risk.

Chemical exposure may contribute to the rise in atopic diseases and needs more research.

Certain gene variations might help protect against insulin resistance and glucose intolerance in people with Polycystic Ovary Syndrome.

Progranulin overexpression leads to shorter, thinner hair and increased cell death in mouse hair follicles.

Certain proteins involved in DNA modification may affect the genetic changes in systemic lupus erythematosus and could indicate the disease's activity.

A woman with acne and baldness was found to have a rare ovarian condition but successfully had a child through fertility treatment.

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.

Mutation in hairless gene may increase hair loss risk.

A three-year-old girl has hair loss despite treatment with selenium sulfide shampoo and anti-fungal medication.

A 12-year-old girl in Saudi Arabia with Focal dermal hypoplasia showed skin and dental symptoms, highlighting the condition's variability and the need for personalized treatment.

An 8-year-old girl has a rare genetic disorder causing complete, irreversible hair loss and skin bumps.

Two sisters have rare hair disorders causing short, fragile, kinky hair.

Not having enough or having too much of the protein Grainyhead-like 3 leads to various developmental problems.

Men with early hair loss may have a higher risk of enlarged prostate and possibly prostate cancer due to shared hormonal factors.

The 2004 hair research meeting presented new findings on hair cell differentiation, genetic factors in hair loss, hair pigmentation, and potential targeted therapies.

Mice treatments didn't grow hair, a patient treatment may affect immune response, and people with hair loss often feel anxious or depressed.