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Hair, skin, and nails supplement use nearly doubled from 2011 to 2020, with higher usage among young adults, females, and certain ethnic groups.

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

Hutchinson-Gilford Progeria Syndrome caused rapid aging due to a genetic mutation, with treatments to manage symptoms.

Corneodesmosin is crucial for skin and hair health, and its dysfunction can cause skin and hair disorders.

HDPCM treatment healed a baby's congenital skin defect caused by varicella infection.

Antiandrogen therapy may be beneficial for women with hidradenitis suppurativa.

EPDS can cause recurring scalp sores and hair loss if not treated.

Woodhouse-Sakati syndrome can cause writer's cramp and other varied symptoms, highlighting the importance of genetic testing for diagnosis.

Careful management of chronic hyponatremia is crucial to prevent severe neurological issues.

The document reports three sisters with Woodhouse-Sakati syndrome showing typical symptoms and unusual gynecological anomalies.

Hidradenitis suppurativa may mainly affect vellus hair follicles, not terminal ones.

HDAC4 and HDAC7 are crucial for Th17 cell development and could be targeted to treat inflammatory diseases.

Higher HDAC1 levels in alopecia areata suggest HDAC inhibitors might help treat it and acne.

Sickle cell disease affects BMI and pain frequency, with HbSS patients having more pain and unhealthy BMI.

More pediatric-specific research and guidelines are needed to improve hidradenitis suppurativa treatment in children and adolescents.

Genetic testing can diagnose hair loss linked to DSG4 gene variants.

The HSD3B1 variant increases hair loss risk in overweight women with PCOS.

LSD1 and HSP90 help heal skin wounds by changing hair follicle stem cells' metabolism.

A mutation in the hairless gene speeds up severe itchy skin in mice on a special diet.

The WAHRS Live Surgery Workshop and Symposium was a unique hair restoration event.

A new DSG4 gene mutation causes hair defects in a young girl.

HHV-6 reactivation may be linked to psychiatric disorders and can improve with antiviral treatment.

A new genetic mutation linked to Hutchinson-Gilford progeria syndrome was found in China.

Early treatment of EPDS can improve outcomes and reduce recurrence risk.

Suppressing the HGPS mutation may improve symptoms and suggest reversibility.