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Hidradenitis suppurativa may be a type of autoinflammatory skin disease linked to gene mutations and immune system issues.

Low-dose glucocorticoid treatment improves pregnancy and birth rates in women with nonclassical 21-hydroxylase deficiency.

A gene mutation in mice causes increased mast cells and disorganized hair follicles in their skin.

The combination of stem cell medium and hydrogel effectively reduces and improves hypertrophic scars.

Pseudomonas DL17 can completely break down the harmful dye Sunset Yellow FCF in 48 hours.

Dihydrotestosterone gel before hypospadias surgery led to less scarring but raised concerns about potential psychological effects and skin changes.

Cutaneous lupus patients have higher levels of certain immune cells in their blood and skin.

Gomez–Lopez–Hernandez syndrome can cause focal hair loss and developmental delays but some children can still function well and excel in school and sports.

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

Spironolactone helps reduce pain and lesions in hidradenitis suppurativa patients, and lower doses are also effective.

Oral minoxidil and growth factors improved hair density and thickness in a girl with hereditary hair loss.

The gene for slick hair in Senepol cattle is located on chromosome 20 and may involve the SRD5A2 gene.

Mutations in the POC1A gene can cause a unique form of extreme insulin resistance and short stature.

A gene mutation causes lanceolate hair in rats by disrupting hair shaft integrity.

The compound (NH4)2Mn0.17Cu0.83Cl4.2H₂O has a specific structure, shows weak magnetism at low temperatures, and undergoes phase changes at high temperatures.

A patient with steroid sulfatase deficiency had a unique hair pattern and a brain malformation not previously linked to the condition.

Family dynamics affect preschoolers' stress levels, especially DHEA.

Bioengineered skin models aging well, useful for studying aging and testing treatments.

Two rare genetic diseases cause severe rickets in children due to defects in vitamin D metabolism.

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

SNP rs2479106 in the DENND1A gene may increase PCOS risk in Saudi Arabian females.

Small molecules can help turn skin cells into sweat gland-like cells for potential skin repair.

PCOS is the main cause of hirsutism, often linked to insulin resistance.

Inhibiting HSP90 increases cell adaptability and survival under stress.

KFSD causes scarring hair loss and skin roughness, mainly in males.

Non-classic congenital adrenal hyperplasia (NCCAH) can mimic PCOS and requires genetic testing for proper diagnosis and treatment.

Familial dyskeratotic comedones are a rare, benign skin disorder that is hard to treat.

The hydrogel speeds up diabetic wound healing by reducing inflammation and promoting skin repair.