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5-alpha-reductase inhibitors may help stabilize or slow down hair loss in some frontal fibrosing alopecia patients, but more research is needed to confirm their effectiveness and safety.

High CRP levels could indicate vitamin D deficiency in people with alopecia areata.

Long-haul COVID can cause lasting symptoms affecting many body systems and may be linked to ongoing inflammation and immune system issues.

Proxalutamide improved recovery, lowered death rates, and reduced hospital stay for COVID-19 patients.

Testosterone undecanoate safely and effectively increased penis size in male children with 5-alpha-reductase deficiency.

Low SULT activity in hair follicles leads to better response to oral minoxidil for hair loss.

Topical ceramide treatment partially improves the skin condition in Jack Russell Terriers with a genetic skin disorder.

Efficient delivery systems are needed for the clinical use of CRISPR-Cas9 gene editing.

The environment around the time of conception can change the VTRNA2-1 gene in a way that lasts for years and may affect disease risk.

Cannabinoids may help treat various skin conditions.

New treatments are needed for PCOS that target its genetic, hormonal, and metabolic causes.

LPA3 signaling in the uterus is crucial for placental formation and fetal development.

Prostasin has two roles in skin: one for normal skin development without needing activation, and another for proper hair growth that requires activation.

A specific gene variant causes severe skin issues and increases infection risk, requiring careful medical monitoring.

Some children in Malaysia with symptoms have either profound or partial biotinidase deficiency, and early testing and treatment are important.

Some skin medications can have harmful interactions with the COVID-19 drug nirmatrelvir-ritonavir, but not with molnupiravir.

Recent findings suggest that genetic factors, immune system issues, and skin cell defects might contribute to the development of hidradenitis suppurativa.

The study found two new mutations in a Chinese patient with severe biotinidase deficiency.

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

Non-classical 21 hydroxylase deficiency is an underdiagnosed cause of female hair loss and polycystic ovarian syndrome.

Recognizing specific skin features helps diagnose and manage lupus erythematosus effectively.

Topical finasteride might be a good alternative for hair loss treatment with fewer side effects, but more research is needed.

The document concludes that understanding hair follicle histology and the hair cycle is crucial for diagnosing alopecia.

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.

Cornification is how skin cells die to form the protective outer layer of skin, hair, and nails.

Vitamin D is important for bones, hair, blood pressure, and breast development.

Biotin and biotinidase are essential to prevent health issues, and deficiencies require lifelong supplementation.

Edar signaling is crucial for proper hair follicle development and function.

Understanding how DHT works is important for diagnosing and treating hormone-related disorders.

Dutasteride treatment in men with mild to moderate COVID-19 reduced viral shedding, inflammation, and recovery time without serious side effects.