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Women with nonclassic congenital adrenal hyperplasia experience more sexual dysfunction and distress.

Acne is significantly influenced by genetics, and understanding its genetic basis could lead to better, targeted treatments.

Children with classic congenital adrenal hyperplasia have thicker heart fat and are at higher risk for heart problems and early atherosclerosis.

Children with classic congenital adrenal hyperplasia have thicker heart fat and more heart and blood vessel risk factors, especially if their condition is not well-controlled.

The spiny mouse is a unique menstruating rodent that can help us understand menstruation and reproductive disorders.

Akt2 protein is essential for normal cell division in early mouse embryos.

Choline and biotin are important for liver health and preventing certain deficiencies in animals, and more research is needed to understand their benefits in humans.

Cancer development is like natural selection, involving mutated cells and environmental factors.

Certain cells in the adult mouse ear come from cranial neural crest cells, but muscle and hair cells do not.

The document reviews key historical figures and discoveries in dermatology.

Coats' Plus is a genetic disorder with eye abnormalities, brain calcification, poor growth, bone and skin issues, and movement disorders.

Androgens are important for normal ovarian function and estrogen production, but may not be the main cause of follicle death.

Patient had scalp allergy from minoxidil; test helped identify cause and suggest alternative treatments.

The conclusion is that future hair loss treatments should target the root causes of hair thinning, not just promote hair growth.

Female donor to male recipient sex mismatch and positive ACA-IgG are key risk factors for vitiligo and alopecia areata in chronic GvHD patients.

The document concludes that ongoing research using animal models is crucial for better understanding and treating Alopecia Areata.

The conclusion is that removing both ovaries is the best treatment for excess male hormones in postmenopausal women, with medication as another option, and managing insulin resistance is important for diagnosis and treatment.

The document concludes that diagnosing PCOS in teenagers is difficult and should focus on specific hormone levels and menstrual irregularities, while also considering treatment for symptoms and related health issues.

Removing a methyl group from the ITGAV gene speeds up bone formation in a specific type of bone disease model.

The conclusion is that standardizing testosterone measurement methods is essential for better diagnosis accuracy in women.

The document concludes that early and personalized treatment for PCOS in adolescents is crucial to manage symptoms and prevent long-term health issues.

Hidradenitis suppurativa is a chronic skin condition more common in women, linked to genetics and lifestyle factors, and associated with various other health issues.

The document concludes that careful history and physical exams are crucial for accurately diagnosing polycystic ovary syndrome and distinguishing it from other similar conditions.

The guidelines recommend informed consent for gender-affirming treatments and stress the importance of personalized, culturally sensitive care for transgender individuals.

The conclusion is that using drugs to block the TOR pathway might slow aging and prevent age-related diseases.

Chemotherapy can cause skin problems like hair loss, mouth sores, and skin darkening, and recognizing these can affect treatment decisions.

Early development of hair, teeth, and glands involves specific signaling pathways and cellular interactions.

The circadian clock influences the behavior and regeneration of stem cells in the body.

Advanced human skin models improve drug development and could replace animal testing.

Different scaffold patterns improve wound healing and immune response in mouse skin, with aligned patterns being particularly effective.