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Oral lichen planus is a chronic disease causing mouth discomfort and sometimes needs immunosuppressive treatment.

Androgen treatment with dihydrotestosterone may help maintain height in patients with 5-α-reductase type 2 deficiency, especially before puberty.

Men and women respond differently to drugs for COVID-19, high cholesterol, and diabetes, which suggests a need for personalized treatments.

Congenital Adrenal Hyperplasia is a rare inherited disease causing hormone imbalances, affecting growth, fertility, and heart health, diagnosed through blood tests and treated with medication and lifestyle changes.

Certain genetic markers on chromosome 20 are linked to hair loss in the Han Chinese from Yunnan.

MicroRNAs are crucial in controlling cell signaling, affecting cancer and tissue regeneration.

Black women with CCCA are more likely to have uterine fibroids.

Hair loss gene found on chromosome 3q26.

Two gene variations, rs6493497 and rs7176005, may be linked to female hair loss in Chinese people.

Women with severe acne, hirsutism, and androgenic alopecia often have higher levels of certain androgens, but the specific pattern can't be predicted just by looking at symptoms.

Some drugs can cause rare but potentially deadly skin reactions, and early treatment and avoiding the drug again are key.

Melanocyte stem cells in hair follicles are key for hair color and could help treat greying and pigment disorders.

The document concludes that alopecia areata is an autoimmune disease without a definitive cure, but treatments like corticosteroids are commonly used.

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

Reduced AR gene methylation may cause early pubic hair growth in girls.

Certain gene variants may contribute to high androgen levels in women with polycystic ovary syndrome.

Scientists identified three genes important for processing certain brain chemicals, thyroid hormones, and medications.

Alopecia areata involves immune response and gene changes affecting hair loss.

Certain genetic markers linked to reproductive potential were identified by their impact on a protein's ability to bind to genes.

The NUDT15 gene variant causes severe side effects from azathioprine in some Indian patients.

Researchers identified genes in scalp hair follicles that may affect hair traits and hair loss.

The Wnt signaling pathway is not a major factor in the development of keratoacanthoma, a type of skin tumor.

PCOS has a strong genetic basis, but more research is needed to fully understand it.

Early treatment of PCOS in teens is crucial to prevent long-term health issues like diabetes and heart disease.

Hidradenitis Suppurativa is a chronic skin condition best treated early with surgery for better outcomes and less recurrence.

These specific gene polymorphisms are not linked to Alopecia Areata in Egyptians.

Skin problems are common in lupus, often appearing first, with various types and treatments, and careful monitoring is important for diagnosis and management.

Patients with Systemic Sclerosis have much higher levels of GDF-15, which could help predict organ involvement and guide treatment.

Gene mutations can cause problems in male genital development.

The document summarizes medical findings on topics like heart rhythm treatment, sleep apnea therapy, and various health conditions and treatments.