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Some people have genetic mutations that make them resistant to vitamin D, leading to rickets even with enough vitamin D intake.

Minoxidil, finasteride, and low-level laser light therapy are effective FDA-approved treatments for hair loss.

AGA treatments like minoxidil and LLLLT are safe and effective for gender minority patients.

The AIRE gene variant rs2075876 is linked to a higher risk of alopecia areata in males.

Certain gene variations might help protect against insulin resistance and glucose intolerance in people with Polycystic Ovary Syndrome.

Higher levels of MiR-92a-1-5p and miR-328-3p found in female hair loss patients.

Twins had rare skin cysts likely due to genetics.

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

Men with a certain baldness pattern at age 40-50 may have a higher risk of aggressive prostate cancer.

Genetics, stress, and health issues can cause early hair greying, which affects self-esteem, and there's no cure, only hair dye.

Androgenetic alopecia in men is genetic and linked to health issues like obesity and heart disease, with treatments including minoxidil, finasteride, and hair transplants.

Doctors should consider Netherton syndrome in patients with chronic skin and hair issues to avoid misdiagnosis.

The guidelines suggest using various treatments, including antidepressants and steroids, for alopecia areata and discuss the condition's genetic and immune aspects.

Rare genetic variants in five specific genes are linked to male-pattern hair loss but only account for a small part of the risk.

Alopecia areata is complex, often recurring, and needs personalized treatment, especially with other health issues.

Studying rare genetic disorders can help us understand and treat common diseases better.

The study suggests that a specific gene variation and higher gene activity are linked to increased baldness in Egyptian men.

The Rotterdam Study updated findings on elderly health, focusing on heart disease, genetics, lifestyle effects, and disease understanding.

The Rotterdam Study found risk factors for elderly diseases, links between lifestyle and genetics with health conditions, and aimed to explore new areas like DNA methylation and sensory input effects on brain function.

The secretome from mesenchymal stem cells is a promising treatment that may repair tissue and avoid side effects of stem cell transplantation.

The Rotterdam Study updated its design and objectives in 2012, providing insights into various diseases in the elderly, including skin cancer, bone health, liver disease, neurological and psychiatric conditions, and respiratory issues.

Insulin resistance and obesity are key factors in the development and worsening of polycystic ovary syndrome, and lifestyle changes are important for managing it.

Oral antiandrogens effectively treat female hair loss, with better results in higher hair loss grades.

Early diagnosis and individualized treatment improve outcomes for Congenital Adrenal Hyperplasia.

Alopecia areata is an autoimmune disease causing patchy hair loss, often with other autoimmune disorders, but its exact causes are unknown.

Male hormones affect COVID-19 severity and certain drugs targeting these hormones could help reduce the risk.

Baldness is more common in Chinese men than women, increasing with age, and is influenced by genetics.

Lichen planus pigmentosus causes dark skin patches and is treated by avoiding triggers and using anti-inflammatory medications.

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

The document concludes that early recognition and treatment of PCOS in adolescents is crucial for managing symptoms and long-term health risks.