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The update highlights that non-classic congenital adrenal hyperplasia is common in women with excess male hormones, requires specific hormone tests for diagnosis, and has various treatment options depending on age and symptoms.

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

Using 17-hydroxyprogesterone levels to diagnose nonclassic congenital adrenal hyperplasia can result in many incorrect diagnoses.

The study concluded that testing hormone levels after stimulation is not reliable for identifying carriers of 21-hydroxylase deficiency; genetic testing is necessary.

Measuring 17-hydroxyprogesterone in hair can help monitor androgen levels in people with congenital adrenal hyperplasia.

A postmenopausal woman's masculine symptoms improved after surgery for a hormone-producing ovarian tumor.

Women with excessive hair growth or polycystic ovary disease may more often carry a gene variant for 21 hydroxylase deficiency.

Adipose stem cell-derived exosomes may improve hair count and scalp health, potentially outperforming current treatments like minoxidil.

Acne not improved by usual treatments may indicate a genetic disorder.

A woman with a specific mutation causing adrenal gland issues faced fertility problems, but careful hormone therapy helped her manage it successfully.

The technique can potentially treat hair loss by using a matrix to grow new hair from cells.

The study found that certain microRNAs are higher in the cells and lower in the fluid of women with a specific type of polycystic ovary syndrome, and one microRNA could potentially help diagnose the condition.

MicroRNA-21 could help diagnose and treat skin fibrosis.

The patient was diagnosed with anorexia nervosa and severe malnutrition, requiring urgent refeeding and monitoring.

A 21-day-old baby had a skin rash that didn't improve with cream and wasn't caused by a fungus.

The LncRNA AC010789.1 slows down hair loss by promoting hair follicle growth and interacting with miR-21 and the Wnt/β-catenin pathway.

Surgery may help infants with sagittal craniosynostosis develop more typical language processing.

A cluster of sulfur-rich hair protein genes was found on chromosome 17.

The study found that Keratosis Pilaris Atrophicans is a genetic skin condition that starts in childhood, involves inflammation and scarring, and current treatments are only somewhat effective.

FGF21 can help reduce skin inflammation caused by C. acnes.

LC-MS/MS is more reliable than immunoassays for diagnosing 21-hydroxylase deficiency.

The KRTAP21-2 gene affects wool length and quality in sheep.

Enobosarm may effectively treat androgen receptor-positive breast cancer with fewer side effects.

TRM21 helps control flavonoid production and root hair growth in Arabidopsis thaliana.

After chemotherapy for early breast cancer, 33.4% of patients had long-term significant hair loss, with some hair regrowth over time, but treatments for hair loss were largely ineffective.

Hydrocortisone 17-butyrate 21-propionate ointment caused reversible side effects like skin issues, weight gain, and organ changes in dogs.

The KRTAP21-1 gene affects wool yield and can help improve wool production.

A young man's hair loss was the only sign of syphilis, which improved after treatment.

Homeopathic remedies can help manage PCOS symptoms in girls aged 17-21.