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The AMHR2-482A>G gene change is linked to higher PCOS risk.

Tumor cells in calcifying epithelioma of Malherbe resemble hair follicle cells.

Ingesting Leucaena leucocephala caused hair loss and increased infant mortality in ringtailed lemurs.

Allopurinol may cause rare granulomatous microscopic colitis.

Trichoscopy can diagnose monilethrix, a genetic hair defect causing hair thinning and loss.

Alpha-difluoromethylornithine prevents cancer in mice but causes hair loss.

Melanocytic matricoma can look like skin cancer but is usually harmless; surgery and follow-up are advised.

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

Reticular erythematous mucinosis syndrome can occur with minimal mucin deposition.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

Monilethrix is a rare, inherited condition causing fragile hair and hair loss, with no cure but some treatments may help.

Pilomatrixoma should be considered for nodular lesions in adults.

Adding Brij 78 to minoxidil microparticles in a certain solution helps them stick to the skin better and prevents clumping.

The SA-MS hydrogel is a promising material for improving wound healing and skin regeneration in diseases like diabetes and skin cancer.

A man with rare skin changes on his fingers was diagnosed with multiple myeloma-linked amyloidosis.

The demineralized bone matrix scaffold is better for cell attachment than the mineralized bone allograft.

Myotonic dystrophy should be considered in patients with hair thinning, and genetic counseling is important.

A Jordanian family with Clouston syndrome has a common GJB6 gene mutation.

Dermoscopy helped diagnose a rare hair disorder in a 2-year-old boy.

New mutations in hair keratin genes can change hair structure and cause monilethrix, with nail issues more common in certain gene mutations.

Topical treatments led to hair regrowth in a man with linear morphea.

Tavaborole is a safe and effective toenail fungus treatment, with the 5% solution being the best option.

A common mutation in the hHb6 gene is linked to monilethrix, but other factors may also play a role.

The E413K mutation in the hHb6 gene causes monilethrix, a hair disorder, but doesn't show consistent symptoms.