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Faulty Notch signalling may cause hair follicle changes and inflammation in hidradenitis suppurativa.

Sebaceous gland atrophy and abnormal function may contribute to hair loss in psoriasis.

A 12-year-old boy with a rare genetic condition has progressive hair loss with no effective treatment.

High prolactin levels can cause skin and hair symptoms similar to those caused by hormone imbalances.

Neurosteroids are crucial for stress response, and targeting specific receptors may help treat certain disorders.

A genetic mutation in a specific gene causes a salt-wasting condition in a Pakistani girl and her family.

A specific gene mutation causes hair loss and potential eye issues, even if vision seems normal.

Tiny particles from brain cells help hair grow by targeting a specific hair growth pathway.

Selenium deficiency caused symptoms in a child, which improved with selenium supplements.

Looser dietary restrictions can improve growth and reduce illness in methylmalonic acidemia patients.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

The mutated hairless gene causes hair loss by acting as a new type of corepressor affecting thyroid hormone receptors.

A new genetic disorder caused by an ODC1 mutation can be treated with DFMO.

The mutant HR bmh protein mis-localizes in cells, affecting skin and hair development.

Human scalp hair follicles can produce and respond to several hormones, affecting hair growth and pigmentation.

The treatment increased hair growth and thickness in patients with hair loss.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

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.

A boy with progeria had eye problems and signs of aging like hair loss and skin wrinkling.

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

Women with acromegaly often have irregular periods due to hormone imbalances and growth hormone effects.

The mutation causes hairless mice due to mislocalized and dysfunctional HR protein.

Umbilical cord blood transplantation improved the boy's symptoms despite complications.

Biotin treatment improves symptoms of biotinidase deficiency, but some neurological damage may be permanent.

A mutation in the Sgkl gene causes defective hair growth in mice.

Woodhouse-Sakati syndrome often causes sexual development issues, hair loss, learning disabilities, deafness, muscle contractions, limb pain, and diabetes.

Stimulating sensory neurons can increase IGF-I production, which may help treat various diseases and improve tissue health.

Delayed puberty affects some teens, and early treatment with hormones can help improve their growth and social well-being.

Two siblings with a genetic mutation had a form of rickets that doesn't respond to vitamin D.