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CD80CD86 deficiency causes hair loss by disrupting regulatory T cells.

Male pattern baldness might have evolved to help protect against prostate cancer by increasing UV radiation on the scalp.

The document reports three sisters with Woodhouse-Sakati syndrome showing typical symptoms and unusual gynecological anomalies.

Rapamycin may help treat Leigh syndrome by targeting protein kinase C.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

Two cases of a rare skin condition were successfully treated with laser therapy, offering a non-surgical treatment option.

The document concludes that early and personalized treatment for PCOS in adolescents is crucial to manage symptoms and prevent long-term health issues.

The document concludes that early diagnosis and a comprehensive treatment plan are crucial for managing hair loss in children, with a focus on both medical and psychological support.

Untreated congenital adrenal hyperplasia can lead to complications like stroke and needs glucocorticoid treatment.

Diagnosing and managing PCOS in teens is hard, but early diagnosis and lifestyle changes are key, and more research is needed for long-term health.

The book provides updated knowledge on hair disorders and new treatments for hair loss.

Diagnose and manage hair issues in women by checking medical conditions and using personalized treatments.

Ellis van Creveld syndrome, a rare genetic disorder, can cause unexpected abnormalities in various body organs, requiring thorough patient evaluations.

An 8-year-old girl had a rare, benign skin tumor on her forehead.

Using cetirizine on the skin and taking vitamin D can help increase hair growth in children with hair loss from ectodermal dysplasia.

Twins had rare skin cysts likely due to genetics.

Ethinylestradiol/chlormadinone acetate may be an effective and well-tolerated treatment for skin conditions caused by excess androgens.

Minoxidil might cause blood vessel-related skin lesions when applied to the scalp.

A rare combination of halo nevi, nonsegmental vitiligo, and early gray hair can occur together.

Getting ethical approval for research with children is important but can be complex and time-consuming, sometimes leading to the exclusion of certain age groups.

The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.

Eight people with severe hair loss grew their hair back naturally.

Hair loss was found in 37.4% of surveyed rural high-school students in Eskisehir, Turkey, affecting their quality of life, especially in general health and mental well-being.

Minoxidil treatment increased hair density in a young Asian girl with short anagen syndrome, but didn't improve hair length or thickness.

A man with a birthmark on his scalp developed hair loss that improved with treatment, but the link between the birthmark and hair loss was unclear.

Treatments for autoimmune hair loss have limited success and often relapse, and emotional support is crucial for those affected.

Green tea extract may help reduce excessive hair growth.

Endoscopy-assisted surgery for craniosynostosis showed excellent outcomes with minimal complications and most patients went home the day after surgery.

Late diagnosis of congenital adrenal hyperplasia can greatly affect physical development, gender identity, and sexual health.

A rare skin disorder affecting the face was found in a 28-year-old Saudi man.