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PRO-C22 can help diagnose and monitor the severity of hidradenitis suppurativa.

A genetic mutation caused severe rickets and alopecia in an Indian patient, but high-dose calcium and phosphate treatment improved their condition.

Certain gene variations may protect against skin issues and oxidative stress in women with PCOS.

DHT affects hair follicle cells by changing microRNA levels, leading to less cell growth and more cell death.

The mutant HR bmh protein mis-localizes in cells, affecting skin and hair development.

Taking 100 mg of DHEA daily for 16 weeks did not change metabolic and reproductive health significantly but increased certain ovarian markers with minimal side effects.

People with alopecia areata had lower vitamin D levels, but these levels did not relate to how severe their condition was.

Hsc70 protein may influence hair growth by responding to androgens.

Urtica dioica extract may help treat androgenic skin diseases by reducing a specific gene's activity.

A substance called compound-1 could help increase hair growth by maintaining prostaglandin levels in hair follicles.

K6/ODC transgenic mice are effective for quickly identifying cancer-causing chemicals.

Low vitamin D can worsen pediatric alopecia areata.

An over-the-counter vitamin/mineral supplement improved hair loss and blood sugar control in a woman with non-classic 11-hydroxylase deficiency.

The treatment was not recommended due to limited effectiveness and significant side effects.

BDNF, TSH, fT4, anti-TPO, and 25-OH Vitamin D levels predict depression risk in patients with autoimmune thyroiditis and hypothyroidism.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

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

Early detection of specific VDR mutations is crucial for effective treatment and better dental outcomes in children with hereditary vitamin D–resistant rickets.

Finasteride effectively inhibits the enzyme steroid 5 alpha-reductase II.

A rare gene variant causes sexual development issues in siblings, needing personalized treatment.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

The mutant HR bmh protein affects hair follicle formation by failing to repress vitamin D receptor activity.

Lack of vitamin D receptor increases skin tumor risk by boosting hedgehog signaling.

Vitamin D and its receptor are crucial for bone health and can be influenced by certain fats and curcumin.

Vitamin D helps regulate calcium levels in the body.

Routine genetic testing is crucial for early diagnosis and better management of Turner’s syndrome with 21-hydroxylase deficiency.

Vitamin D receptor interacts with certain dietary components to help prevent diseases and regulate hair growth.