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Human hair follicle stem cells can become smooth muscle cells using specific growth factors.

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

The study aims to find new risk factors and early signs for heart and brain diseases to improve prevention and management.

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

The new method improves bone repair by enhancing cell loading and stability in bioprinted scaffolds.

The treatment improved hair growth in people with male pattern baldness.

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

Mutations in specific genes disrupt development of sweat glands, teeth, hair, skin, and nails in HED.

Complex basal cell carcinomas need personalized treatment due to unique genetic mutations.

Mutations in the DSG4 gene cause fragile, sparse hair in humans, mice, and rats.

hHb1, hHb3, and hHb6 mRNAs start expressing at the same time in hair follicles.

The patient had complex urinary tract issues and ambiguous genitalia, with physical features suggesting a hormonal imbalance.

Altering the keratin 17 gene in mice hair follicles caused temporary hair issues, but changes were minimal and short-lived.

Higher androgen levels during puberty are linked to shorter adult height in boys with Silver-Russell syndrome.

Lower family income is linked to more stress in parents and more behavior problems in children.

Improving access to hidradenitis suppurativa care can reduce social disparities.

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

A new hair restoration technology was found to effectively increase hair thickness, density, and growth, while reducing hair loss and improving scalp health, with no side effects.

Recent findings suggest that genetic factors, immune system issues, and skin cell defects might contribute to the development of hidradenitis suppurativa.

Hedgehog pathway inhibitors for advanced basal cell carcinoma can cause side effects, but managing them helps maintain treatment.

Adults with Tatton-Brown-Rahman syndrome may have serious heart problems and need lifelong heart monitoring.

Certain genes and high cholesterol levels increase heart disease risk in Ethiopian patients with high blood pressure.

Lhx2 is a crucial regulator of the Sonic Hedgehog signaling in early mouse retinal development.

A 13-year-old boy with a rare genetic condition survived a heart attack and improved with treatment.

Hair sensitivity to androgens is partly controlled by specific enzyme expressions in different hair areas.

Hepatitis B vaccination can trigger HSP, and vitamin D correction and tonsillectomy can effectively manage it.

The Bethesda system is effective for identifying thyroid cancer but has low sensitivity.

Hormones might affect the skin condition hidradenitis suppurativa, but their exact role is unclear.

Increasing PBX1 reduces aging and cell death in hair follicle stem cells by boosting SIRT1 and lowering PARP1 activity.

About 3% of high school girls aged 14-18 in Isfahan, Iran, have polycystic ovary syndrome.