Search

everythinglearnresearchcommunity

for

Search:↓

Hormonal imbalances during menopause may significantly contribute to Frontal Fibrosing Alopecia.

A rare gene variant causes sexual development issues in siblings, needing personalized treatment.

RSPO1 mutations in certain patients lead to skin cells that don't develop properly and are more likely to become invasive, increasing the risk of skin cancer.

Females have a higher lifetime risk of alopecia areata than males.

No consistent link between genotype and phenotype in 5-α-Reductase type 2 deficiency.

Alopecia Areata is linked to a higher risk of several diseases, which vary with age and sex.

New genes and pathways are important for testosterone production and male sexual development.

Finasteride has a higher risk of reproductive side effects than minoxidil.

Two new reliable Arabic questionnaires for measuring quality of life in women with PCOS were created, one for married and one for unmarried women.

People with reproductive, thyroid disorders, and type 2 diabetes can experience voice changes, but more research is needed to understand this better.

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

Sebaceous glands play a key role in skin health, immunity, and various skin diseases.

Chicken feather gene mutation helps understand human hair disorders.

Gender affects hair and scalp characteristics, with differences in hormone responses, graying patterns, and trace metals.

Men and women react differently to opioids, with hormones potentially influencing these differences.

Androgens affect many aspects of female health, and more research is needed to understand their roles and treatment potential.

Titanium dioxide nanoparticles may harm the male reproductive system.

Understanding hair growth involves complex interactions between molecules and could help treat hair disorders.

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

Melanocyte development from neural crest cells is complex and influenced by many factors, and better understanding could help treat skin disorders.

Insufficient androgen action in male fetuses can cause genital development issues due to genetic mutations or environmental chemicals.

The questionnaire is valid and reliable but needs more testing for future predictions.

Congenital Adrenal Hyperplasia is a genetic disorder with two forms, causing symptoms like early puberty and severe acne, but can be identified through screening and treated with glucocorticoids.

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.

Women with PCOS are more than twice as likely to develop nonalcoholic fatty liver disease.

A Saudi individual initially identified as a girl had a genetic disorder affecting gender development.

Hormone imbalances can cause specific skin changes, which may help in early detection of endocrine disorders.

Steroid cell tumors in the ovary are rare, can produce testosterone causing symptoms, and are mainly treated with surgery.

SHBG may be a useful early indicator and treatment target for PCOS.

Men and women have different levels and production of brain steroids, which may affect their risk for certain brain disorders.