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Basonuclin 2 is vital for the development of facial bones, hair follicles, and male germ cells in adult mice, and its absence can lead to dwarfism and abnormal follicles.

Buffalo flies and Stephanofilaria nematodes cause severe skin lesions in beef cattle, and treatment should target both.

Hormones during puberty increase certain receptors in the brain, and this change is influenced by estrogen levels.

Spironolactone helps reduce fluid in the eye in Central Serous Chorioretinopathy, but doesn't improve vision and recurrence is common.

5α-Reductase inhibitors may increase depression risk but not dementia or suicide.

K6hf is a unique protein found only in a specific layer of hair follicles.

The 190-kbp domain contains all human type I hair keratin genes, showing their organization and evolution.

LY191704 is a compound that effectively blocks a specific enzyme involved in hormone conversion and could help treat enlarged prostate and hair loss.

Finasteride effectively treats male pattern hair loss with a 1 mg daily dose.

Keratin 17 is modified by RSK1 in response to growth and stress, affecting skin growth and stress response.

MK-386 and finasteride together effectively reduce DHT levels, potentially treating acne and male pattern baldness.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

Finasteride, when given in high oral doses to pregnant monkeys, caused genital abnormalities in male fetuses, but not in female fetuses or those exposed to intravenous finasteride.

Finasteride effectively treats male hair loss, improving growth and density.

A fragment of human type XVII collagen shows great potential for skin health and wound healing.

A mutation in the KRT82 gene is significantly associated with Alopecia Areata.

People with myotonic dystrophy type 1 have a higher chance of getting skin tumors, including melanoma.

A man with myotonic dystrophy type 1 had 28 skin cancers, suggesting a link between the disease and skin cancer, emphasizing the need for sun protection and regular skin checks.

Metformin for PCOS can rarely cause side effects like joint pain and behavior changes.

A rare genetic disease causes rickets and often hair loss in young children, which can improve with specific treatments.

A woman with a rare hormone resistance condition also had missing teeth and hair loss, which might be new symptoms of her genetic disorder.

A child with a rare vitamin D-resistant condition improved with treatment.

A 21-year-old male with a rare genetic disorder experienced sudden hair loss and high DHEAS levels, likely due to a condition similar to PCOS, usually seen in women.

A girl with a rare genetic disorder had a unique bone condition, highlighting the need for careful diagnosis and suggesting the disorder might be more common than thought.

A rare endocrine disorder, APS 1, was diagnosed in a 26-year-old man in Bangladesh.

A 28-year-old man with type 1 diabetes had skin and hair issues due to zinc deficiency.

Autoimmune Polyendocrine Syndromes involve specific combinations of endocrine and non-endocrine autoimmune diseases.

Type 3 Innate Lymphoid Cells help maintain skin health and balance, and are involved in skin diseases and healing.

A child with a rare type of rickets showed some improvement with high doses of vitamin D, but such conditions often respond poorly to treatment.

Rothmund-Thomson syndrome type 2 can cause chronic, poorly healing wounds.