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A strict gluten-free diet can improve liver issues in celiac disease.

Persistent papular plaques on children's faces need better understanding and treatment.

Genetic testing confirmed a rare skin disorder in a young girl, which improved with zinc supplementation.

The method accurately measures cyproterone acetate in plasma, showing no significant difference between two formulations.

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

A gene mutation in mice causes severe skin disorder similar to a human condition.

CTCF protein is essential for skin and hair follicle development in mice.

H1 increases risk for neurodegenerative diseases, while H2 offers protection but is linked to other disorders.

cDermo-1 causes dense skin, feathers, and scales in chickens.

A genetic mutation in the CDH3 gene causes hair loss and vision problems in a young Saudi girl.

The ACE1 gene variant doesn't affect long-COVID symptoms.

Not having the gene PLAAT3 leads to fat loss, high insulin resistance, and abnormal fat levels in the blood due to a disruption in fat cell development and function.

Some people's hair loss is caused by multiple factors, with the most common being a mix of AGA and CCCA.

JAM-A helps hair regrowth in alopecia areata by protecting VCAN in skin cells.

A boy with a new NR5A1 gene mutation has a sex development disorder without affecting his adrenal glands.

CD44 variant changes start alopecia areata, but don't maintain it.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

DAB labeling effectively identifies collagen type III and PDGFR in horse skin, but may show false positives.

Drug repositioning offers hope for new, affordable treatments for a genetic skin disorder called ARCI.

Understanding how EDC genes are regulated can help develop better drugs for skin diseases.

Lower MC2R expression may contribute to alopecia areata.

AKR1C3 could be a treatment target for metabolic issues in PCOS.

Tofacitinib effectively improved severe skin symptoms in a patient with Hypohidrotic Ectodermal Dysplasia.

A new genetic mutation in the CDH3 gene causes hair loss and eye problems in young people.

Acrodermatitis enteropathica can be linked to dental issues, so thorough dental exams are important.

Targeting NMMHC IIA may help treat blood-brain barrier damage.

Genetic marker rs12558842 strongly linked to male hair loss.