Search

everythinglearnresearchcommunity

for

Search:↓

Researchers found potential urine markers for polycystic ovary syndrome, including testosterone-glucuronide and 11α-hydroxyprogesterone, which may help diagnose the condition.

Epidermolytic ichthyosis can be inherited in a semidominant way with mild symptoms in carriers.

Scientists found a new gene in a bacterium that can modify an immunosuppressant drug, potentially helping to treat hair loss.

LSD1 is essential for healthy skin development and creating the skin's protective barrier.

Bolandiol, a synthetic steroid, builds muscle and bone without greatly affecting sex glands, and works differently from other hormones.

Loss of COL17A1 causes hair follicle stem cells to age and leads to hair loss.

DHEA treatment helps grow pubic hair and boosts mood in girls with adrenal issues.

People with hypohidrotic ectodermal dysplasia are more likely to experience long-term fatigue and hair loss after COVID-19.

A woman's masculine symptoms were caused by a rare tumor in her left ovary, which was found using a special blood test.

Zinc supplements improved the girl's skin and hair condition.

People with PCNT mutations often develop severe insulin resistance and early-onset diabetes during childhood or adolescence.

Two new gene mutations cause a rare hair disorder.

About 50% of 46, XY DSD cases lack a genetic diagnosis, but advanced sequencing methods improve detection.

A boy's early puberty caused by a testicular tumor returned to normal after surgery.

Idiopathic hirsutism is the most common cause, followed by PCOS, and insulin resistance should be checked in patients with acanthosis nigricans.

A 6-year-old boy developed excessive hair growth after taking diazoxide for low blood sugar.

A bull with a gene mutation was asymptomatic, synthetic retinoids cause hair loss, and new therapeutic targets were identified for skin diseases.

Tofacitinib helps improve skin conditions in people with Down syndrome, especially alopecia areata.

Genetic mutations cause various hair diseases, and whole genome sequencing may reveal more about these conditions.

Hormones might affect the skin condition hidradenitis suppurativa, but their exact role is unclear.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

Dihydrotestosterone has a reduced effect on muscle-building in people with testicular feminization syndrome, especially after their gonads are removed.

Patients with a specific genetic variant have more severe alopecia areata and higher recurrence rates.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

Early diagnosis and aggressive treatment are essential for managing Vogt-Koyanagi-Harada syndrome effectively.

A WNT10A gene mutation leads to ectodermal dysplasia by disrupting cell growth and differentiation.

Scientists found new, better-working inhibitors for a hormone-related enzyme.

Deleting the scd1 gene in mice prevents obesity by disrupting skin lipids and improving heat regulation.