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

Botulinum toxin type A helps treat hair loss by stopping cell death in hair follicles through a process involving certain non-coding RNAs and a protein called Bax.

Cationic and nonionic surfactants provide better color intensity and resistance for semi-permanent hair dye than anionic surfactants.

Laser treatment for hair loss works equally well on different skin types, but more research is needed for very dark skin.

A woman's hair grew back after treatment for a rare hair loss caused by proton therapy.

There is no cure for myotonic dystrophy type 1, so treatment focuses on managing symptoms and complications.

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.

Testosterone and dihydrotestosterone treatments can help with penile growth in males with 5α-reductase type 2 deficiency, with dihydrotestosterone being more effective in infancy.

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.

Two siblings with a rare type of rickets and hair loss had low vitamin D levels, which is not typical for their condition.

Autoimmune Polyendocrine Syndromes involve specific combinations of autoimmune diseases.

KIF18B is important for correctly positioning cell division machinery in skin cells, affecting hair follicle development.

A man with a fungal scalp infection got better after treatment with griseofulvin, cetirizine, and ketoconazole shampoo.

Innate lymphoid cells type 1 may contribute to alopecia areata.

Innate lymphoid cells type 1 may contribute to alopecia areata by damaging hair follicles.

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

Patients with one autoimmune disease should be checked for other autoimmune disorders.

WNT10B is linked to cancer development and affects survival and disease progression in various cancers.

Blocking 11β-HSD1 reduces stress hormone damage in hair growth cells.

A boy with Oculodentodigital syndrome had a unique GJA1 gene mutation causing his symptoms.

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

Laminin-511 is involved in psoriasis development and can be regulated by cannabinoid receptor type 1.

A patient with a rare chromosome condition also had a rare type of hair loss.

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.

Botulinum toxin type A reduces itch and inflammation from histamine and may help treat certain skin conditions and hair loss.

The document's conclusion cannot be provided because the document is not available or cannot be read.

MK-386 reduces sebum DHT levels.

Eating less calories, focusing on complex carbs, and reducing fats can help manage type II diabetes.

Compound 4 is a promising treatment for hair loss with low toxicity.