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Metformin, usually used for diabetes, can also help treat hair loss from alopecia areata due to its ability to reduce inflammation and stimulate new hair growth.

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

New tools show that in fish, NPY increases feeding and somatostatin decreases it.

Anti-Ro exposed children had more reported neuro-psychiatric issues, but differences from healthy controls were not significant.

Hair cortisol could be a marker for chronic stress in pregnancy, but depression affects cortisol levels differently.

Understanding skin structure and development helps diagnose and treat skin disorders.

Testosterone therapy seems safe and effective for transgender men with proper care, but more long-term research is needed.

Familial factors affect hair loss types in Koreans, with M type in men, L type in women, and paternal factors influencing male hair loss more.

The newborn with Klippel-Trénaunay syndrome was healthy but needed regular check-ups for possible complications.

The guideline recommends mental health involvement in diagnosing gender identity disorder and outlines hormone and surgical treatment protocols, emphasizing safety, informed consent, and long-term monitoring.

Male and female bodies respond differently to stress, influenced by hormones and development stages, with implications for stress-related diseases.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

New research suggests that skin cell renewal may not require a special type of cell previously thought to be essential.

Transplant success has improved with better immunosuppressive drugs and donor matching.

Insulin sensitizers may slightly reduce hirsutism but are less effective than other treatments.

Scientists turned mouse stem cells into skin cells that can grow into skin layers and structures.

Phospholipase A2 is necessary for the correct placement of PIN proteins in plant roots, affecting root growth.

Despite progress, better treatments and understanding are needed for the high rates of long-term issues and deaths linked to eating disorders.

Certain mutations in the H6PD gene cause Cortisone Reductase Deficiency by affecting hormone production.

Liver transplantation is a viable option for children with propionic acidemia, improving quality of life and diet, but does not remove all risks and long-term brain outcomes are uncertain.

LGR5 helps maintain corneal cell characteristics and prevents unwanted changes by controlling specific cell signaling pathways.

Some parents have a mild form of congenital adrenal hyperplasia without symptoms, and they usually don't need treatment.

Researchers found 71 genetic regions linked to male pattern baldness, which account for 38% of its genetic risk.

About 8.5% of women in Salvador, Brazil, have Polycystic Ovary Syndrome.

Alopecia areata is linked to thyroid autoimmunity but not type 1 diabetes.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

Diagnosing PCOS in teenagers is hard because its symptoms often look like normal puberty, and there's a need for better diagnosis methods and agreement on criteria.

Testosterone therapy can improve sexual desire and function in postmenopausal women but should be used cautiously and not based solely on testosterone levels.

Teens with PCOS and a mom with PCOS have higher insulin resistance and lower adiponectin levels, which could signal early metabolic problems.

Ozone therapy might improve cancer treatment and reduce its side effects.