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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.

Up to 50% of scalp hair can be lost before it appears thin, and treatment is only needed for hair loss caused by diseases or deficiencies.

Two siblings were found to have a genetic condition causing progressive hair loss and woolly hair, which may often be misdiagnosed.

Taking vitamins, minerals, and amino acids can improve hair strength and quality in people with Monilethrix.

Light microscopy is useful for diagnosing different hair disorders.

Scarring alopecias are complex hair loss disorders that require early treatment to prevent permanent hair loss.

Genetic variants in PDE6H and LPAR6 cause vision impairment and hair loss in two Pakistani brothers.

Hair thinning causes stem cell loss through a process involving Piezo1, calcium, and TNF-α.

Genetic testing is crucial for diagnosing congenital atrichia, a rare condition causing irreversible hair loss.

Understanding hair growth involves complex factors, and more research is needed to improve treatments for hair loss conditions.

Alopecia areata, a type of hair loss, is likely an autoimmune disease with a genetic link, but its exact cause is still unknown.

New treatments like low-level laser therapy, platelet-rich plasma therapy, and micro needling show positive results for hair regrowth in people with genetic hair loss.

Alopecia areata causes patchy hair loss and has no cure, but treatments like corticosteroids and minoxidil can help.

Children's hair loss can have various causes, including infections, autoimmune issues, physical stress, nutritional problems, and genetic factors.

Certain immune molecules and stress affect hair loss, and while genes play a role, more research is needed to fully understand and treat it.

A specific gene mutation causes varying hair loss severity in a Pakistani family.

Monilethrix causes fragile, patchy hair loss.

A 12-year-old girl was diagnosed with monilethrix, a genetic condition causing fragile, beaded hair that breaks easily, with no effective treatment available.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

The guide helps doctors diagnose hair problems by suggesting a thorough patient history, physical exams, and various diagnostic tools.

Alopecia Areata is an autoimmune condition causing hair loss with no cure and treatments that often don't work well.

New treatments for hair loss from alopecia areata may include targeting immune cells, using stem cells, balancing gut bacteria, applying fatty acids, and using JAK inhibitors.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

Alopecia areata can be triggered by specific immune cells without genetic or environmental factors.

Alopecia areata is caused by the immune system attacking hair follicles.

CCCA is a common hair loss condition in African American women, often inherited and influenced by hairstyling, with unique scalp features detectable by special tools.

Alopecia areata is caused by immune system issues, and JAK inhibitors might help treat it.

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.

New research has found 14 genes linked to the risk of developing alopecia areata, improving understanding and treatment options.