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Early baldness in men may indicate risks for obesity, metabolic syndrome, insulin resistance, and heart disease, similar to women with PCOS. Alopecia areata is often linked with autoimmune diseases and mental health issues. Certain hair disorders are due to genetic issues, and chemotherapy can cause hair loss through specific biological pathways. Iron deficiency's link to hair loss is still disputed.

Early balding, especially frontal, increases prostate cancer risk; more research needed.

Early hair loss in men could be a sign of non-cancerous prostate enlargement, and treating hair loss early might help prevent prostate issues later.

Early balding in men might be a male hormonal equivalent of polycystic ovaries syndrome in women.

Early treatment of traction alopecia can reverse hair loss; prevention involves avoiding tight hairstyles.

Focal atrichia helps diagnose female pattern hair loss.

A 4-year-old girl with hair loss was diagnosed with early-onset trichotillomania and improved with behavioral interventions.

SA linked to mitochondrial issues and oxidative stress, while AGA involves disrupted hair growth genes.

Metabolic syndrome can cause serious health issues and should be considered when treating women with severe acne.

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.