Search

everythinglearnresearchcommunity

for

Search:↓

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

Genetic defects in androgen production are linked to male developmental disorders and are improving treatment understanding.

Genetic defects in testosterone production can cause hormonal and developmental disorders, and more research is needed to understand androgen regulation and develop safer treatments.

Curcuma aeruginosa Roxb. may help treat hair loss by affecting specific biological pathways.

The conclusion is that while oral contraceptive pills are effective for PCOS-related high androgen levels, new treatments with fewer side effects are needed.

The document concludes that blocking the internal pathways that create androgens might help treat cancers that depend on sex hormones.

The document concludes that early diagnosis and treatment of Congenital Adrenal Hyperplasia are crucial for preventing serious health issues and improving patient outcomes.

Androgens like testosterone are important hormones for both men and women, made differently in each sex and affecting the body by regulating genes and quick interactions with cell components.

Neuroactive steroids and the enzyme 5α-reductase might be involved in the development of Tourette's syndrome.

Mice without the enzyme HSD17B3 still produce normal testosterone, suggesting they have different ways to make it compared to humans.

The research identified genes and non-coding RNAs in cells that could be affected by testosterone, which may help understand hair loss and prostate cancer.

Finasteride and dutasteride reduce neurosteroid production, possibly helping treat glioblastoma.

The document concludes that the 5 alpha-reductase enzymes are important in steroid metabolism and related to various human diseases, with inhibitors used to treat conditions like male pattern baldness and prostate issues.

Early diagnosis and individualized treatment improve outcomes for Congenital Adrenal Hyperplasia.

The update highlights that non-classic congenital adrenal hyperplasia is common in women with excess male hormones, requires specific hormone tests for diagnosis, and has various treatment options depending on age and symptoms.

The document concludes that proper diagnosis and a multidisciplinary approach are crucial for managing Congenital Adrenal Hyperplasia effectively.

With careful management, people with congenital adrenal hyperplasia can have successful pregnancies and become parents.

Blocking DHT production more strongly may help control advanced prostate cancer and improve quality of life.

The severity of symptoms in nonclassical congenital adrenal hyperplasia is not determined by CYP21A2 gene variations.

Finasteride affects SRD5A2 gene pattern, possibly causing lasting side effects.

11α-Hydroxyprogesterone is changed into different substances by certain enzymes and may play a role in prostate cancer.

Genetic variations affect dutasteride treatment response for male pattern hair loss.

Excess androgens may cause PCOS, not just be a symptom.

Diagnosing sex development disorders requires combining medical history, physical exams, imaging, lab tests, and genetic data.

The document concludes that patient outcomes for Congenital Adrenal Hyperplasia are often not ideal because of poor management and a need for better diagnosis and treatment methods.

Gene mutations can cause problems in male genital development.

Certain drugs like Dutasteride and Finasteride might help fight SARS-CoV-2 by increasing levels of a steroid called DHEA, which can protect the heart and increase nitric oxide to counteract the virus.

Sex hormones, especially androgens, play a key role in causing acne.

Understanding how DHT works is important for diagnosing and treating hormone-related disorders.

A new method accurately measures nine specific hormones in human blood.