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Most children with a common hemochromatosis genotype had elevated iron levels but no severe symptoms.

A genetic change in the EDAR gene causes the unique hair traits found in East Asians.

An 84-year-old man developed a rare scalp condition from a cancer drug but continued treatment as it was otherwise well tolerated.

Higher activity in lichen planopilaris is linked to certain immune and tissue genes.

A unique gene mutation was found in a family with monilethrix.

Cell detachment, not autoantibody binding, causes major changes in pemphigus.

New research on prostamide F2α has led to treatments for glaucoma and eyelash growth and may have more medical uses.

CRABP1 boosts hair cell growth in Hu sheep by affecting key genes.

The model can effectively test gene functions and drug responses in human skin.

A specific genetic mutation may increase male pattern baldness risk, especially in Europeans.

The treatment effectively reduces hair loss and improves hair growth with minimal side effects.

Plaque-type herpetic folliculitis affects eccrine glands.

CTIP2 may help in skin development and maintenance.

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

Somatic BHD mutations are rare in Japanese renal tumors.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

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

Human TMEM2 does not break down hyaluronan but helps control its metabolism.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

OsUEV1B protein is essential for controlling phosphate levels in rice.

Mutations in the ABCB6 gene cause Dyschromatosis Universalis Hereditaria.

EGF and EGFR are important for goat skin development, increasing from weeks 6 to 21.

A Brazilian male with IFAP syndrome has a unique genetic variant causing his condition.

PNH can occur in patients with SLE, so doctors should be aware of this.

Overexpression of the HE4 gene in mice causes eye inflammation and cloudiness.

People with alopecia areata have higher levels of EGF in their blood than healthy people.

New mutations in MBTPS2 reduce its function and cause IFAP syndrome with unusual symptoms.

EGF and KGF signalling prevent hair follicle formation and promote skin cell development in mice.

VEGF promotes hair follicle cell growth through the VEGFR-2/ERK pathway.

Markers help differentiate between apocrine and eccrine sweat glands to identify sweat gland tumors.