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Patients with Focal Dermal Hypoplasia often experience skin, nail, hair, and bone issues, and may benefit from calcium and vitamin D supplements.

A new method accurately measures DHEAS in blood, improving on current tests.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

Squaric acid dibutylester for alopecia areata can cause benign skin lymphoid growths.

A 12-year-old boy had severe shingles and skin damage after a stem-cell transplant.

A new group called the Asian Association of Hair Restoration Surgeons (AAHRS) has been created.

DHEA supplementation may improve quality of life, neuropsychological functions, and sexual satisfaction in individuals with adrenal insufficiency, but more research is needed to confirm its safety and effectiveness.

Unique genes in hair follicle cells help tissue regeneration.

VKHD and sarcoidosis may share a common cause.

Untreated Sheehan's Syndrome caused severe heart failure in a woman, which improved with hormone and heart failure treatment.

Treating PCOS patients with HP HMG significantly raises the risk of ovarian hyperstimulation syndrome, needing careful dose management.

Botulinum toxin type A may help treat hidradenitis suppurativa.

Botulinum toxin type A injections may help treat hidradenitis suppurativa.

People with hidradenitis suppurativa have a higher risk of kidney stones.

Human dermal stem/progenitor cells can divide and differentiate more than hair follicle dermal papilla cells.

Hidradenitis suppurativa tunnels have different microenvironments, suggesting targeted treatments could be more effective.

Hair coloring and bleaching can permanently break down hair protein and temporarily change its properties.

IL-26 has antimicrobial and pro-inflammatory effects in the chronic skin condition Hidradenitis Suppurativa.

Antiandrogen therapy may be beneficial for women with hidradenitis suppurativa.

KFSD is a rare condition causing scarring hair loss, with no effective treatment known at the time of the report.

Hdac1 and Hdac2 help maintain and protect the cells that control hair growth.

Childhood growth hormone deficiency can be accurately diagnosed using gene expression data and random forest analysis.

Children with classic congenital adrenal hyperplasia have thicker heart fat and more heart and blood vessel risk factors, especially if their condition is not well-controlled.

Higher DHEA-S levels in hirsute females affect hair growth phases.

HLA can be linked to autoimmune hepatitis.

Adalimumab is the most effective treatment for severe hidradenitis suppurativa, but more research is needed to improve treatment options.

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

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

The report shows a young man with Hutchinson-Gilford Progeria Syndrome had typical and additional eye problems related to the disease.