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A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

High doses of Tridax procumbens extract can be toxic, affecting liver and kidneys.

People with vitiligo may have a lower risk of heart disease.

A rare genetic skin condition usually affecting males was found in a 9-year-old girl.

Using buccal mucosa for hypospadias repair in children is effective and reduces complications.

Adults with atopic dermatitis showed similar adherence to different forms of hydrocortisone cream, but actual use varied despite self-reports of near-perfect usage.

Some children who had stem cell transplants developed permanent hair loss, especially when treated with a drug called busulphan.

Low TRPS1 expression in skin and hair cells is linked to hair problems in Trichorhinophalangeal syndrome.

A 17-year-old boy with Temporal Triangular Alopecia successfully grew new hair after a hair restoration surgery using follicular unit transplantation.

The monkey's hair loss was due to an autoimmune disease, not genetics.

A 10-year-old girl with Fox Fordyce disease improved with treatment, suggesting the disease can occur before puberty and might be underdiagnosed in young girls.

The multi-injection plate is a less painful and more efficient method for treating patchy hair loss.

SEPA™ enhances the effectiveness of minoxidil in stimulating hair growth, working faster and better than Rogaine® TS, with no significant side effects.

Using minoxidil lotion for hair regrowth in androgenetic alopecia has limited success and should be evaluated carefully.

P-cadherin is important for hair growth and health, and its problems can cause hair and skin disorders.

Zouboulis syndrome is a rare condition that helps diagnose monosomy 18p early.

The X5 Hairlaser might help treat male hair loss, but more research is needed.

Some patients treated with peginterferon and ribavirin for chronic hepatitis C had mild to moderate skin reactions, but treatment did not need to be stopped.

An 11-month-old boy with Menkes disease had severe brain shrinkage and abnormal blood vessels, and didn't respond well to treatment.

FGF-1 causes spiral ganglion neurites to branch more.

Alopecia areata causes hair loss due to an immune attack on hair follicles, influenced by genetics and environment.

Finasteride helps treat hair loss by blocking enzyme activity.

Hair regrowth doesn't convert thin hairs to thick hairs, but increases overall hair density.

Low doses of BPA can increase prostate growth and change hormone levels in adult rats.

Acitretin significantly reduced inflammatory attacks in a woman with Naevus Comedonicus Syndrome but caused side effects.

Phyto-vesicles of β-sitosterol may effectively treat hair loss.

A Japanese patient with IFAP syndrome had a severe MBTPS2 gene mutation but showed milder symptoms than previously observed cases.

Canadian porcupines in a Japanese zoo passed a skin fungus to each other.

UVA1-light therapy successfully treated a child's skin condition, mycosis fungoides.

The cause of alopecia areata was unknown, and while various treatments existed, no best treatment was agreed upon.