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Woodhouse-Sakati syndrome often causes sexual development issues, hair loss, learning disabilities, deafness, muscle contractions, limb pain, and diabetes.

Micro-segmental hair analysis helps detect drug use patterns and estimate drug consumption days.

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

The engineered yeast strain BLYAS can quickly and sensitively detect androgenic chemicals.

SSO helps in skin protection and keratinization.

Early diagnosis using eye tests and lab markers can improve treatment for pediatric Sjögren's syndrome.

The Spanish HSS-29 scale effectively measures changes in life quality due to female-pattern hair loss.

In STSD patients, the body compensates for low androgen levels by increasing another enzyme's activity.

QMSI effectively maps and quantifies drug distribution in skin tissues.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

Microsponges delivery system is a safe, versatile method for controlled drug release in various treatments.

Higher testosterone and dehydroepiandrosterone sulphate levels may help diagnose meibomian gland dysfunction.

Early diagnosis and management of Sheehan's syndrome are crucial for improving quality of life and fertility.

A systems biology approach helps improve mesenchymal stromal cell therapies by mapping interactions and identifying treatment targets.

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

MSM supplementation in kittens improves hair quality and growth rate without harming their health.

scMC effectively separates biological signals from technical noise in single-cell genomics data.

Sulfur mustard damages hair follicles and sebaceous glands in mice.

In Japan, sex reassignment surgery for gender identity disorder faces challenges and needs better medical support and education.

Altering SSAT affects fat metabolism and body fat in mice.

The school nutrition program improved students' health and reduced vitamin deficiency symptoms.

A woman with EMS showed unusual skin mucinosis without the typical hard skin syndrome, suggesting EMS can cause skin mucinosis.

Three new techniques simplify and improve the preparation of tissue samples for skin cancer surgery.

The enzyme steroid sulfatase is linked to breast cancer and other conditions, and inhibitors are being developed for treatment.

Loss of Msx2 function causes eye development issues similar to Peters anomaly.

Sox13 is a marker for early hair follicle development but not essential for skin and hair growth.

The TT genotype of a specific SNP in sheep is linked to better wool quality.

Toluidine blue helps accurately diagnose and treat certain skin tumors in surgery.

A 21-month-old boy has a rare genetic disorder causing sparse hair due to an LSS gene mutation.