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AGA, a common hair loss, is caused by genetics, hormones, age, and environmental factors.

Six genetic conditions are often linked to complete scalp hair loss in children.

Stem cell niches are crucial for regulating stem cell behavior and tissue health, and their decline can impact aging and cancer.

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

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

AGA more common in men, Koreans have lower rates and unique patterns.

The document concludes that more research is needed to better understand and treat primary cicatricial alopecias, and suggests a possible reclassification based on molecular pathways.

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

Alopecia areata is a genetic and immune-related hair loss condition that is often associated with other autoimmune diseases and does not typically cause permanent damage to hair follicles.

New treatments for Alopecia Areata show promise but need to be more effective and affordable.

New genetic locations explain much of hair color variation in Europeans.

New methods have greatly improved our understanding of stem cell behavior and roles in the body.

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

Kennedy's disease leads to muscle weakness and sensory issues, has no cure but manageable symptoms, and future treatments look promising.

Hair loss gene found on chromosome 3q26.

The cause of Frontal Fibrosing Alopecia is unclear, diagnosis involves clinical evaluation and various treatments exist, but their effectiveness is uncertain.

Genetic differences between young and old Tan sheep explain why their fleece changes from curly to straight as they age.

DNA variants can predict male pattern baldness, with higher risk scores increasing baldness likelihood.

The research suggests that the global distribution of PCOS is likely due to historical human migration and that genes affecting PCOS may have different impacts on males and females.

Hair diversity is influenced by complex genetics and environmental factors, requiring more research for practical solutions.

Genes play a significant role in male-pattern baldness, and understanding them could lead to new treatments and insights into related health issues.

Certain genetic markers, especially the MICA gene, are linked to alopecia areata.

Female pattern hair loss has unclear causes, possibly involving genetics, hormones, and environment, and needs better treatments.

Gene therapy has potential as a future treatment for Hutchinson-Gilford progeria syndrome.

Men's hair loss is caused by hormones and genes, and can be treated with medication and surgery, while graying is due to aging and has no prevention except dyeing.

Mice are useful for researching human hair loss and testing treatments, despite some differences between species.

Some congenital hair disorders improve in childhood or with treatments like minoxidil and retinoids, while others like Netherton syndrome and trichothiodystrophy have a poor prognosis.

Brothers of women with PCOS tend to have higher levels of a hormone called DHEAS, indicating a possible genetic link.

The study found that Central Centrifugal Cicatricial Alopecia mainly affects middle-aged African descent women, is linked to certain hair care practices and genetics, and often goes undiagnosed for years.

Methotrexate effectively treated a 2-year-old's generalized pustular psoriasis without side effects.