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Ultrasound can help detect early signs and severity of hidradenitis suppurativa.

Tissue expansion successfully treated alopecia in a child with hypohidrotic ectodermal dysplasia.

The 3D scaffold helped maintain hair cell traits and could improve hair loss treatments.

Human stem cells were turned into cells similar to those that help grow hair and showed potential for hair follicle formation.

Patients at dermatology specialist hospitals had lower death and readmission rates but higher treatment costs.

Patients with hidradenitis suppurativa have a different skin microbiome compared to healthy people.

DSDs are birth conditions causing unusual sex development, managed with personalized care and sometimes surgery, but still lack a standard treatment approach.

Addressing psychosocial symptoms can improve outcomes for people with Hidradenitis Suppurativa.

Early recognition and treatment of hidradenitis suppurativa in children are crucial to prevent complications.

About 2.2% of women with symptoms of high male hormones have a mild form of congenital adrenal hyperplasia, and measuring a specific hormone level can accurately diagnose it.

Sex hormones may be linked to inflammation in Hidradenitis Suppurativa.

The patient with a misplaced pituitary gland and interrupted pituitary stalk is being treated with hormone replacement.

Hydrogel microneedles offer a promising, minimally invasive way to treat diseases like cancer and hair loss, but need improvements in strength and standardization.

Most hair dyes can cause allergic reactions, so test before use.

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

A unique gene mutation causes vitamin D-resistant rickets without causing hair loss.

3D-cultured cells in HGC-coated environments improve hair growth and skin integration.

Trichoscopy can diagnose Netherton syndrome without pulling hairs.

Two sisters with Netherton's syndrome had skin and hair issues, needing special diet and ointments.

Enriching the French health care database with external data greatly improved its usefulness.

Hairless protein can block vitamin D activation in skin cells.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

Trichoscopy is a helpful tool for diagnosing Netherton syndrome.

Finasteride and DEHP exposure during development can change reproductive markers in rats.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

Hydrogel-forming microneedles are a safe and effective method for delivering drugs through the skin.

A woman's scalp condition improved with specific ointment after a hair piece caused skin issues.

Researchers successfully made new compounds for hormone level tests, but one attempt led to an unexpected product, correcting a past error.

Drospirenone can hide symptoms of certain hormonal disorders, complicating diagnosis.

Mutations in the vitamin D receptor cause hereditary vitamin D-resistant rickets, leading to poor bone health and requiring high calcium doses for treatment.