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Children's hairlines change shape as they grow, with women often developing a widow's peak and men's hairlines becoming more convex and possibly balding at the temples, influenced by genetics and hormones.

Women with PCOS in Sicily show different levels of metabolic problems depending on their PCOS type, with obesity and abnormal lipid profiles being common.

A patient with Satoyoshi syndrome improved with a treatment combining several medications, including carbamazepine and methotrexate.

The document suggests that there might be an autoimmune link between polycystic ovary syndrome and Graves' disease.

A 10-year-old girl with Fox Fordyce disease improved with treatment, suggesting the disease can occur before puberty and might be underdiagnosed in young girls.

Minoxidil 5% solution significantly improved hair density in a girl with loose anagen hair syndrome over 28 months, with no side effects.

Fox Fordyce disease might be more common in prepubertal girls than thought and can be managed with treatment.

Found different long non-coding RNAs in balding Chinese men, which may help create new treatments.

The document emphasizes the importance of correctly identifying and classifying genetic hair disorders to help diagnose related health conditions.

Hair microscopy is useful for diagnosing hair disorders, but clear definitions are needed for accurate genetic analysis.

Fox Fordyce disease can occur in prepubertal girls and may be underdiagnosed.

Extra virgin olive oil may boost the immune system and help fight infections like COVID-19.

Collecting hair for cortisol analysis is possible in low-income mother-toddler pairs.

Hair gels may cause split ends in children.

Cantu syndrome, which causes excessive hair growth and skin issues, is due to a mutation in the ABCC9 gene, and understanding this could help develop new treatments for hair diseases.

Monkeys with hair loss during pregnancy showed higher stress hormone levels and invested differently in their offspring.

Most hair loss in children is caused by a few common conditions and is easy to diagnose, but rare types require careful evaluation.

A boy with a rare form of early puberty caused by a new gene mutation responded well to treatment aimed at reducing testosterone and preserving adult height.

Relatives of women with PCOS symptoms are more likely to have similar health issues.

The document concludes that various hair and scalp disorders in children have specific treatments and proper diagnosis is essential.

Environmental cues can change the fate and function of epithelial cells, with potential for cell therapy.

Spironolactone may help treat excessive hair growth in girls, but more research is needed.

Treating a boy's scalp infection was challenging because two different colors of the same fungus appeared.

A new mutation linked to partial Androgen Insensitivity Syndrome and prostate cancer was found in a patient unhappy with their female gender assignment.

A teenage girl with a fungal scalp infection got better with antifungal and allergy medication, and special shampoo.

PCOS is a complex condition linked to hormonal imbalance and insulin resistance, with weight loss being important for management.

Diagnosing simple-virilizing congenital adrenal hyperplasia can be difficult and requires thorough testing and expert advice.

Woodhouse-Sakati syndrome can cause writer's cramp and other varied symptoms, highlighting the importance of genetic testing for diagnosis.

Children with cancer had slightly more unusual facial shapes than healthy kids, but not enough to easily tell them apart.

Intense pulsed-light therapy helps mice grow hair by activating a specific growth pathway.