Search

everythinglearnresearchcommunity

for

Search:↓

A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

The document says that understanding the causes of PCOS is important for treatment, especially in distinguishing the syndrome from just having cystic ovaries, and that losing weight is key for obese women with PCOS.

The document concludes that the exact way alcohol causes harm to fetal development is unknown, but it significantly affects nutrient transport to the fetus and a safe level of alcohol during pregnancy is not determined.

Notch/CSL signaling controls hair follicle differentiation through Wnt5a and FoxN1.

AE can have varied symptoms and genetic causes, but zinc therapy helps.

Acute telogen effluvium can be resolved by addressing causes, but chronic telogen effluvium is harder to treat.

Activating β-catenin in different skin stem cells causes various types of hair growth and skin tumors.

A genetic mutation in the EDA gene causes hypohidrotic ectodermal dysplasia in cats.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

Scientists found a gene in mice that causes early hearing loss.

Men's hair loss is caused by hormones and genes, and can be treated with medication and surgery, while graying is due to aging and has no prevention except dyeing.

Hair turning darker can be a sign of skin cancer.

Stress in hair follicle stem cells causes inflammation in a chronic skin condition through a specific immune response pathway.

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

Cyproterone acetate treatment is safe and causes mild feminization, which increases with added estrogen.

AGA in children needs careful diagnosis due to low androgen levels and possible other causes.

Pulse steroid therapy for alopecia areata shows a 43% complete response rate but has a high relapse rate, especially in children.

COVID-19-related hair loss may have unique features compared to hair loss from other causes.

The Rotterdam Study aims to understand disease causes in the elderly and has found new risk factors and genetic influences on various conditions.

A child's hair loss after Kawasaki disease may help understand the disease's autoimmune causes.

Hair shedding is an active process that could be targeted to treat hair loss.

Up to half of women by age 50 experience significant hair loss, with various types and treatments available.

Erectile dysfunction is increasingly common in men under 40, with many physical and psychological causes, and various treatment options available.

Activating autophagy in dogs with certain diseases improves their skin and hair.

Fibrodysplasia ossificans progressiva is a rare genetic disorder that causes extra bone growth and symptoms of premature aging.

The two-factor model fits better for Chinese patients' understanding of illness causes than the original four-factor model.

Most women with hirsutism have normal hormone levels and can be treated with cosmetic methods; obesity and PCOS are common causes, and treatments depend on the underlying issue.

Researchers found a specific immune receptor in patients that causes severe skin reactions to a drug.

Polycystic ovary syndrome and iron overload share similar symptoms and can be potentially treated with blood removal, diet changes, and probiotics.

Androgenetic alopecia, or hair loss, is caused by a mix of genetics, hormones, and environment, where testosterone affects hair growth and causes hair to become smaller and grow for a shorter time.