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A genetic test can identify people at risk of male pattern baldness early, allowing for quicker treatment.

Segmental Vitiligo is a stable, early-onset form of vitiligo that responds well to early treatment and is ideal for repigmentation studies.

Hair loss can be an early sign of prostate enlargement.

The guideline suggests using specific criteria to diagnose PCOS, recommends various treatments for its symptoms, and advises screening for related health issues.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

Multiple eye conditions were studied, highlighting the importance of various imaging methods for diagnosis, the vision side effects of drugs tamoxifen and Propecia, and the usefulness of optical coherence tomography for diagnosing and monitoring macular and retinal diseases.

The enzyme RDH12 plays a role in vision and retinal disease, with mutations leading to early onset visual loss and blindness, but the exact disease mechanism is unclear and there are no treatments yet.

A man with myotonic dystrophy type 1 had 28 skin cancers, suggesting a link between the disease and skin cancer, emphasizing the need for sun protection and regular skin checks.

Hair loss in men treated best with early medication or transplant, new treatments researched.

New hair loss treatments may include topical medications, injections, and improved transplant methods.

There may be a link between hair loss and heart disease in women, but more research is needed.

Clomipramine may significantly reduce hair-pulling in Trichotillomania, but more research is needed on treatments and early onset cases.

Recent selection on immune response genes was identified across seven ethnicities.

Three siblings with a genetic form of rickets showed different symptoms of the disease.

Low selenium levels can extend lifespan but worsen health issues.

The document discusses various challenging skin conditions and their treatments.

A gene mutation in mice causes increased mast cells and disorganized hair follicles in their skin.

A new peptide, FOL-005, may help treat excessive hair growth by reducing a hair growth promoter, FGF7.

Some skin conditions may indicate metabolic syndrome, which could help with early detection and management of related health issues.

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

Two mouse mutations cause similar hair loss despite different skin changes.

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

Younger transgender women have surgery earlier, are mostly attracted to men, and show more preoperative depression that improves after surgery compared to older transgender women.

A certain genetic variation in the IL1A gene may lower the risk of a hair loss condition in Chinese people.

Preventing cancer involves lifestyle changes, vaccinations, early screening, and understanding cancer's molecular basis.

Minoxidil and finasteride are effective for treating hair loss, with dutasteride showing potential but with side effects.

Ferulic acid helps stabilize vitamins C and E for better skin protection from the sun, certain compounds may promote hair growth, atopic dermatitis patients have lower skin defense molecules, older men are more likely to get a type of skin cancer, and a substance called relaxin may prevent age-related skin thickening.

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

No link found between new male baldness genes and female hair loss.

People with hair loss have higher risk of high blood sugar and diabetes, and lower levels of a specific hormone.