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A certain genetic variation is linked to a higher risk of polycystic ovarian syndrome.

A genetic variant in the androgen receptor gene increases heart disease risk in women but not in men.

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

A woman's unique dementia was misdiagnosed, a genetic mutation increases Parkinson's risk with age, and finasteride may help with Tourette syndrome.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

Cyproterone acetate may cause liver cancer at high doses, but is considered safe at recommended doses for approved uses.

A Saudi individual initially identified as a girl had a genetic disorder affecting gender development.

Higher levels of miR-203 may contribute to hair loss in alopecia areata.

Androgens like testosterone affect skin health and can lead to conditions such as acne and hair loss, with various treatments available.

Alopecia Areata is an autoimmune condition causing hair loss with no cure and treatments that often don't work well.

Half of people with Alopecia Areata may see hair regrowth within a year without treatment, but recovery is unpredictable.

Hair loss and aging are caused by the breakdown of a key protein in hair stem cells.

The document concludes that the 5 alpha-reductase enzymes are important in steroid metabolism and related to various human diseases, with inhibitors used to treat conditions like male pattern baldness and prostate issues.

Male pattern baldness involves genetics, hormones, and needs better treatments.

Guidelines for diagnosing common hair loss include detailed history, clinical examination, and various diagnostic techniques.

GABRA2 gene variations impact alcohol response, and hair loss medication finasteride reduces some effects.

Targeting androgen receptors could be a promising way to treat skin disorders with fewer side effects.

Male hormones and their receptors play a key role in hair loss and skin health, with potential new treatments being explored.

5α‐reductase isozymes are crucial for prostate development and health, and targeting them can help prevent and treat prostate issues.

The document concludes that early diagnosis and treatment of Congenital Adrenal Hyperplasia are crucial for preventing serious health issues and improving patient outcomes.

Cholesterol sulfate buildup due to a genetic mutation disrupts the skin barrier, leading to the scaling skin seen in X-linked ichthyosis.

COVID-19 can cause various skin lesions, which may result from the virus and immune response, and are not directly linked to illness severity.

A new gene, JMJD1C, may affect testosterone levels in men.

Wnt signaling is crucial for skin and hair development and its disruption can cause skin tumors.

Natural 5AR inhibitors effectively improve mild to moderate hair loss in men.

Plant extracts effectively reduce hair loss and increase growth, offering a safe alternative treatment.

Polycystic Ovary Syndrome is linked to higher risk of hypertension and heart disease.

A49T gene variant linked to higher prostate cancer risk, lower hormone levels, and slightly reduced balding risk.

Nonclassic adrenal hyperplasia is a genetic condition that can cause early puberty and fertility problems, treated with specific steroids.

Impaired androgen production in 46,XY DSDs causes ambiguous genitalia and requires long-term care.