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Mutations in the WNT10A gene can cause skin, hair, teeth, and other disorders, and may also affect other areas like kidney and cancer, with potential for targeted treatments.

Certain HSD3B1 gene types are linked to worse prostate cancer outcomes and affect treatment response and other health conditions.

Hedychium spicatum has medicinal properties but needs more research for scientific validation and use.

Acanthosis nigricans is a skin condition that may indicate a higher risk for insulin resistance and type 2 diabetes, and more research is needed to understand and treat it.

The conclusion is that better understanding and more research are needed to effectively manage follicular and scarring disorders in skin of color, with an emphasis on patient education and cultural awareness.

Oral zinc sulphate reduces dark hair color in mice.

The document concludes that early diagnosis and treatment are crucial for children with hair loss to prevent permanent damage, although not all conditions can be effectively treated.

Finasteride and minoxidil are effective FDA-approved treatments for androgenetic alopecia.

Most hair loss in children is caused by a few common conditions, and it's important to diagnose these properly and support the child's mental health.

Acne is significantly influenced by genetics, and understanding its genetic basis could lead to better, targeted treatments.

Recent genetic insights show that low-renin hypertension includes a range from essential hypertension to secondary or familial forms, affecting diagnosis and treatment.

Certain genetic variations are linked to increased androgen levels in PCOS, but more research is needed to understand these connections fully.

Alopecia areata is an autoimmune hair loss condition treated with corticosteroids, and histologic confirmation is the best diagnosis method.

Hair disorders are caused by a complex mix of biology, genetics, hormones, and environmental factors, affecting hair growth and leading to conditions like alopecia.

The document concludes that accurate diagnosis and treatment of scalp itch require differentiating between various conditions using a proposed five-step evaluation process.

At least 87% of Indian men experience hair loss, with type II being most common and severity increasing with age.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

Most hair loss can be diagnosed with patient history and physical exam, and a few common types make up most cases.

Changes in keratin affect skin health and can lead to skin disorders like blistering diseases and psoriasis.

Patients with GATA2 deficiency show early skin symptoms that help diagnose the condition.

Hair loss involves immune responses, inflammation, and disrupted signaling pathways.

Daughters of women with PCOS generally experience normal puberty but may have more body hair and different body fat distribution.

The document concludes that primary scarring alopecias cause permanent hair loss, have unpredictable outcomes, and lack definitive treatments, requiring personalized care.

Stump-tailed macaque best for researching hair loss causes and treatments.

AIRE-deficient rats developed severe autoimmune disease similar to APECED, useful for testing treatments.

The protein Par3 is crucial for healthy skin, affecting the skin barrier, cell differentiation, and stem cell maintenance.

Premature hair graying in young Turkish adults is more likely if they have stress, a family history of graying, drink alcohol, have chronic diseases, are older, or are taller.

Hair loss risk is influenced by multiple genes.

Male pattern baldness affects 38.52% of Asian men in Bangkok, increasing with age and influenced by genes and environment.

The document concludes that certain mutations may contribute to the inflammation in hidradenitis suppurativa and suggests that targeting TNFα could be a treatment strategy.