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Farudodstat may effectively treat alopecia areata by protecting hair follicles without harmful effects.

Mutations in the hairless protein gene cause hair loss.

Adding dutasteride to therapy may improve treatment for advanced salivary duct cancer.

Rabbits lacking the Hoxc13 gene show similar hair and skin issues to humans with ECTD-9, making them good for research on this condition.

The study found key factors in the cause of hidradenitis suppurativa, its link to other diseases, and identified existing drugs that could potentially treat it.

A 6-year-old girl had a rare allergic reaction to a hair regrowth treatment.

Children with classic congenital adrenal hyperplasia have thicker heart fat and are at higher risk for heart problems and early atherosclerosis.

HSD3B1 gene variant and being overweight linked to hair loss in women with polycystic ovary syndrome.

Finasteride helped treat a 28-year-old's facial skin condition.

A man with kidney tumors and lung cysts was diagnosed with Birt–Hogg–Dubé syndrome and treated successfully, with genetic testing confirming the diagnosis.

A new genetic variant of Woodhouse-Sakati syndrome was found in two adult sisters in Russia.

Squaric acid dibutylester effectively treats alopecia areata.

High DHEA-S levels may cause hair loss in young men.

Dihydrotestosterone (DHT) is crucial for conditions like male-pattern baldness and acne, and measuring a byproduct, androstanediol glucuronide, is a better way to assess DHT's effects than DHT blood levels.

No strong link between testosterone or DHEAS levels and acne or hair loss in females.

High-stress mothers had lower hair cortisol than low-stress mothers, and daughters' cortisol was linked to their stress response.

Hair diameter diversity helps assess hair loss, but its standard measure varies by individual and ethnicity.

HGF combined with ADA is highly accurate for diagnosing tuberculous pleural effusion, especially in younger females.

HASHA is a safe and effective option for chin augmentation.

Squaric acid dibutylester promotes hair growth by activating immune cells, especially macrophages.

A 4-year-old girl had a rare hair disorder affecting only part of her scalp.

Researchers found a new mutation causing total hair loss from birth.

Vitamin D receptor and hairless protein are essential for hair growth.

rwSALT accurately measures hair regrowth in alopecia areata using scalp photos.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

Interface dermatitis is the most common skin change in drug-induced hypersensitivity syndrome.

Intense pulsed light with radiofrequency showed mixed results in improving quality of life for hidradenitis suppurativa patients, with no clinical improvements.

Three siblings with a rare genetic condition had abnormal sexual development and chose different gender identities, needing surgery and therapy.

Uncombable hair syndrome causes frizzy hair and can affect the nervous system, eyes, and ears, often co-occurring with other hair, skin, nail, and teeth conditions, and is linked to three specific gene mutations.