Search

everythinglearnresearchcommunity

for

Search:↓

A 19-year-old male with delayed puberty was successfully treated for a condition that prevents normal hormone production.

Androgenetic alopecia, or hair loss, is caused by genetic factors and hormones, with different mechanisms in men and women, and can be linked to insulin resistance and polycystic ovary syndrome.

Men's sensitivity to male hormones might affect how severe COVID-19 gets for them.

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

Skin varies in thickness, color, and features due to complex genetic and cellular processes.

Female mice with disrupted 5α-reductase 1 had significant metabolic issues, including stress response problems, insulin resistance, liver fat buildup, and obesity.

Certain genes influence immunoglobulin levels in Chinese Holstein cows, which can improve calf health.

Most patients with alopecia areata in China have patchy hair loss, with total hair loss being less common, and the condition often starts around age 35 and can negatively affect quality of life, especially in more severe cases.

Alopecia areata has different forms and can significantly affect quality of life, especially in more severe cases.

The study concluded that patients with total hair loss and recurring hair loss had an earlier onset, longer-lasting condition, and a greater negative impact on their quality of life, with allergic conditions linked to more severe hair loss.

Turning white fat into brown-like fat could help fight obesity and type 2 diabetes.

Scientists turned mouse stem cells into skin cells that can grow into skin layers and structures.

Acne is a chronic disease linked to various systemic conditions and has significant psychological and social effects.

Certain mouse strains develop a skin condition similar to a human hair loss disease due to genetic defects.

Mutations in the hairless gene in mice affect its expression and lead to a range of developmental issues in multiple tissues.

Certain gene variants may contribute to high androgen levels in women with polycystic ovary syndrome.

Hair loss treatments work better with lifestyle changes.

Boys with less severe EDA mutations in XLHED have milder symptoms and better sweat and hair production.

Woodhouse-Sakati syndrome often causes sexual development issues, hair loss, learning disabilities, deafness, muscle contractions, limb pain, and diabetes.

Toxic Epidermal Necrolysis is a rare, serious skin condition that can affect anyone, is more common in women, and may be linked to genetics, with a 20% mortality rate mainly due to sepsis.

The document concludes that Rabson-Mendenhall syndrome requires novel treatments for insulin resistance and emphasizes the importance of dental care in affected patients.

Lupus treatment requires a combination of drugs and therapies, with research needed for new options.

A certain gene variant may increase the risk of polycystic ovary syndrome in Chinese women.

Testosterone therapy improved physical and social health in a male with 49,XXXXY syndrome.

Polycystic Ovary Syndrome (PCOS) symptoms vary globally, with bloating, high cholesterol, and glucose levels being common; the current diagnostic criteria may need refining.

Woodhouse-Sakati syndrome shows varied symptoms, including hair loss and diabetes, and is common in Qatar due to a specific genetic variant.

Pili torti is a rare condition where hair is twisted and breaks easily, often linked to genetic disorders or other health issues.

Specialized techniques are needed for hair restoration in individuals with curly Afrocentric hair due to unique challenges.

Removing anthrax toxin receptor 1 in pigs prevents Senecavirus A infection and causes a rare disease similar to GAPO syndrome.

Albumin and prednisone improved symptoms in a woman with Cronkhite-Canada syndrome, revealing potential genetic causes.