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LGR5 is a marker found in hair follicle stem cells in various species and is important for hair growth and skin repair.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

A man had two rare autoimmune diseases that might be connected.

Hoyeraal-Hreidarsson syndrome in infants causes severe gastrointestinal issues.

The document concludes that treatment improved skin lesions but not scalp hair loss in two patients with Graham-Little-Piccardi-Lassueur syndrome.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

Most transgender patients getting laser hair removal before gender-affirming surgery are already on hormone therapy, which might affect the hair removal process.

A new mutation in the human glucocorticoid receptor reduces its function and causes resistance to glucocorticoids.

Surgery with a carbon-dioxide laser successfully treated a Labrador's tongue condition, but some hair regrew.

Hairline-lowering surgery effectively reduces a high hairline with immediate, noticeable results.

LRIG1 is linked to better survival in Merkel cell carcinoma.

Dermoscopy helps diagnose rare GLPLS in males.

A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

Gene therapy has potential as a future treatment for Hutchinson-Gilford progeria syndrome.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

Hutchinson-Gilford Progeria Syndrome causes rapid aging due to a gene mutation, with no cure yet, but research may lead to better treatments.

Adding licorice gel to laser treatment is more effective for reducing facial hair than laser alone.

SLHA can be hard to diagnose and needs teamwork between specialists.

Using a hair removal laser can make hairs finer for better hairline correction in hair transplants, with most patients happy and few side effects.

Lnc056 helps hair follicle stem cells grow by increasing TRIP6 expression.

Hairless protein affects hair follicle structure by regulating the Dlx3 gene.

Patients with lichen planus should be tested for hepatitis C.

Hormone therapy for excessive hair growth is as good with GnRHa as with high-dose CPA, but GnRHa has longer-lasting results.

Mutations in the hairless protein gene cause hair loss.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

An infant with Hutchinson-Gilford Progeria Syndrome had successful surgery to fix breathing issues caused by a new genetic mutation.

The L457(3.43)R mutation in the human lutropin receptor causes increased activity and hormone insensitivity, leading to precocious puberty.

A new genetic variant in the LIPH gene causes hair growth issues in a Chinese patient.