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Skin-derived stem cells grow faster and are easier to obtain than hair follicle stem cells, but both can become various cell types.

Early diagnosis of Trichorhinophalangeal syndrome type 1 is crucial for treatment and was achieved through clinical examination and family history.

Pediatric endocrinologists should provide early fertility counseling and preservation options to young patients at risk of infertility.

Researchers made stem cells from human hair follicle cells with better efficiency than from skin cells.

New cancer treatments aim to reduce side effects and improve effectiveness.

Hair steroid measurement is an effective method to diagnose and monitor CAH in developing countries.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.

Certain DNA regions in alpacas are linked to fiber diameter.

A girl with type 1 diabetes developed a serious eye condition very early, suggesting the need for earlier eye checks and that early treatment can work well.

Dihydrotestosterone makes arteries stiffer in female mice by reducing estrogen receptor expression.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

Androgen treatment with dihydrotestosterone may help maintain height in patients with 5-α-reductase type 2 deficiency, especially before puberty.

More research is needed to understand how testosterone is maintained in adult males.

Conditions affecting sex development show that sexual diversity is a natural part of human variation.

Skin can produce blood cells, often due to disease, which might lead to new treatments for skin and blood conditions.

Herpes gestationis is linked to certain antigens, atopic eczema affects T cell populations and may be eased by breastfeeding, higher doses of anti-androgen treatment can improve androgenic alopecia, topical minoxidil increases hair thickness, long-term methotrexate therapy can cause liver fibrosis in psoriasis patients, and Lichen Sclerosus et Atrophicus patients aren't at higher risk for autoimmune disorders.

Busulfan/cyclophosphamide and total bone irradiation are equally effective for AML transplants.

Three siblings with a rare genetic condition had abnormal sexual development and chose different gender identities, needing surgery and therapy.

Regenerative cellular therapies show promise for treating non-scarring hair loss but need more research.

VEGF helps squamous cell carcinoma grow in ways beyond just blood vessel formation.

Genetic research has advanced our understanding of skin diseases, but complex conditions require an integrative approach for deeper insight.

Different stem cells have benefits and challenges for tissue repair, and more research is needed to find the best types for each use.

Hormonal imbalances are a key cause of missed menstrual periods in women.

Zouboulis syndrome is a rare condition that helps diagnose monosomy 18p early.

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

A new mutation linked to partial Androgen Insensitivity Syndrome and prostate cancer was found in a patient unhappy with their female gender assignment.

Molecular diagnostics help identify genetic defects causing endocrine diseases, improving diagnosis and treatment options.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

Female relatives of PCOS patients have a higher chance of showing PCOS symptoms.

Various dermatologic treatments were effective for skin conditions like acne, rosacea, hair loss, and psoriasis from December 1986 to December 1987.