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Finasteride may cause lasting sexual and mental health issues, and genetic screening could help prevent them.

Certain genetic variants are linked to frontal fibrosing alopecia in Spanish patients.

Certain immune system genes are linked to a higher risk of psoriasis and psoriatic arthritis, while others may offer protection.

Transplant success has improved with better immunosuppressive drugs and donor matching.

Minoxidil can cause deadly skin reaction; monitor patients closely.

A 33-year-old woman with PCOS and metabolic syndrome was unusually diagnosed with a bone condition called DISH, suggesting a possible link between these conditions.

Individualized treatment and psychological support are crucial for alopecia.

Tacrolimus causes fewer acute rejections than cyclosporin A in kidney transplants but doesn't necessarily improve kidney function after one year; cardiovascular risks and side effects vary between the two drugs.

The severity of symptoms in nonclassical congenital adrenal hyperplasia is not determined by CYP21A2 gene variations.

3D culture helps maintain hair growth cells better than 2D culture and identifies key genes for potential hair loss treatments.

The authors suggest that 5-α-reductase inhibitors, like dutasteride, are effective in treating frontal fibrosing alopecia and should be the first-line treatment, with other options for severe cases. They also recommend further research on Janus kinase inhibitors.

In Singapore, most skin reactions to drugs were in females and Chinese, often caused by painkillers, antibiotics, and some other drugs, with serious cases linked to genetics.

Thyroid diseases may contribute to autoimmune skin diseases, and more research is needed on their relationship.

Congenital Adrenal Hyperplasia is a genetic disorder with two forms, causing symptoms like early puberty and severe acne, but can be identified through screening and treated with glucocorticoids.

Chronic kidney disease can cause skin problems that affect patient quality of life, and treating these conditions can improve outcomes.

Siblings with signs of virilization should be tested for non-classical congenital adrenal hyperplasia, which does not affect adult height but may impact fertility and well-being if untreated.

Hair follicles are normally protected from the immune system, but when this protection fails, it can cause hair loss in alopecia areata.

Personalized medicine in dermatology uses molecular biomarkers to improve diagnosis and treatment but needs further advancements for practical use.

The index to ring finger ratio may indicate disease severity in female ankylosing spondylitis patients, but not in males.

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

Botulinum toxin type A significantly reduces scalp psoriasis severity compared to placebo.

Hashimoto thyroiditis is an autoimmune disease that can lead to an underactive thyroid and is treated with medication and sometimes diet changes or surgery.

Immune cells in Hidradenitis suppurativa become more inflammatory and may be important for treatment targets.

Familial frontal fibrosing alopecia is rare, mostly affects women, and often occurs between sisters or mother-daughter pairs.

Amniotic allograft may be more effective than platelet-rich plasma for midface aging treatment.

People with advanced chronic kidney disease often have skin problems, which can be treated with various medications and procedures to improve their quality of life.

COVID-19 vaccination does not significantly increase the risk of developing alopecia areata.

Antibiotics often cause skin reactions, making them a major health concern.

A young child with complete hair loss improved significantly with a combination of hair growth treatments and laser therapy.

The report concludes that PCOS is mainly a condition of excess male hormones and its definition may change as new information is discovered.