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Melatonin may help with nerve pain, a hepatitis C drug is effective but has side effects, a treatment for mouth sores works but can cause blood issues, ear reconstruction with an implant is safe, HIV transmission from mother to child in Taiwan is now 0% with treatment, certain blood problems are more common in people with a tongue condition, a gene and being overweight are linked to hair loss in some women, a new technique could reduce radiation for lung nodule patients, a hepatitis treatment may lower cancer recurrence after a procedure, and adding extra screening improves tuberculosis detection in patients with lung infections.

The document suggests treating individuals with nonclassic congenital adrenal hyperplasia who show symptoms, especially those related to excess male hormones.

Nonclassic adrenal hyperplasia is a genetic condition that can cause early puberty and fertility problems, treated with specific steroids.

Hair follicle hyperplasia is common in both benign and malignant skin lymphoproliferative disorders, with a proposed new term "pseudolymphomatous adnexitis."

People who carry the 21-Hydroxylase Deficiency gene are not more likely to have excessive male hormone levels.

A person with a specific gene mutation had extra teeth, unique jaw and hair features not seen before in this condition.

A man with hypoparathyroidism had other health issues that led to a diagnosis of a rare autoimmune disorder, APS-1.

The prolactin gene polymorphism doesn't affect cashmere quality in these goats.

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.

Different types of androgens bind differently to two receptors, AR1 and AR2, in Atlantic croaker's brain and ovarian tissues, suggesting these receptors may control different androgen actions in fish.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

Low TRPS1 expression in skin and hair cells is linked to hair problems in Trichorhinophalangeal syndrome.

Selective breeding caused the unique curly hair in Mangalitza pigs.

Different hair loss types need accurate diagnosis for proper treatment.

AMH levels can't reliably tell the difference between LOCAH and all types of PCOS in women with excessive hair growth.

Genetic differences within ethnic groups may affect prostate cancer treatment effectiveness.

Certain genetic changes in the KAP22-1 gene are linked to better wool quality in Egyptian sheep.

Hair loss is linked to heart disease and metabolic syndrome, and while current treatments vary in effectiveness, more research is needed for better solutions.

The study found that a specific genetic variation in the TNFα gene is significantly linked to Alopecia Areata in the Jordanian Arab population.

Common variants in the Trichohyalin gene are linked to straight hair in Europeans.

Imaging helps detect adrenal gland issues and monitor treatment in congenital adrenal hyperplasia, and can identify tumors affecting fertility.

New models predict male pattern baldness better than old ones but still need improvement.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

The document discussed hair loss causes and treatments but didn't give a final summary.

The C-allele and CC-genotype in the PTPN22 gene lower the risk of alopecia areata.

Tioconazole cream is highly effective and easy to use for treating sheep dermatophytosis.

A certain mutation in the fetal alpha 5-reductase gene is linked to a higher risk of late miscarriage.

The document concludes that non-binary individuals need compassionate support and recognition in healthcare, without being pathologized.

Niosomes are a promising, stable, and cost-effective drug delivery system with potential for improved targeting and safety.

Beard hair follicles have more androgen receptors than non-balding scalp hair follicles.