Search

everythinglearnresearchcommunity

for

Search:↓

Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

T-cell reconstitution after thymus transplantation can cause hair whitening and loss.

Chemical exposure may contribute to the rise in atopic diseases and needs more research.

A man with Woolly Hair Syndrome had very curly, fragile hair, and doctors used a special scalp examination to diagnose him without invasive tests.

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

Finasteride blocks deoxycorticosterone's anticonvulsant effects in infant rats, but indomethacin doesn't.

A patient with Werner syndrome showed a range of aging-like symptoms and metabolic issues, underscoring the need for early detection and treatment.

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.

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.

Bardet-Biedl syndrome may include under-recognized skin problems related to its metabolic disturbances.

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

The conclusion is that dermatologists can improve women's skin health but must overcome cultural and economic barriers to do so.

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.