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Congenital Adrenal Hyperplasia is a rare inherited disease causing hormone imbalances, affecting growth, fertility, and heart health, diagnosed through blood tests and treated with medication and lifestyle changes.

Some lesser-known causes of PCOS include autoimmune issues, genetic mutations, and changes in the body's microbiome.

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

Finasteride may cause lasting sexual and mental health issues, and genetic screening could help prevent them.

Benzothiazepines like diltiazem reduce anxiety in mice by making neurosteroids.

Some patients taking finasteride or dutasteride may have ongoing sexual problems and depression even after stopping the medication.

Finasteride almost fully depletes allopregnanolone in rat brains and enhances 20α-DHP, but doesn't change 3α-DHP levels.

Finasteride affects alcohol intake in male mice, possibly due to neurosteroids.

Low doses of mixed chemicals cause permanent reproductive malformations in male rats.

Finasteride may affect fetal brain development and increase arousal, but more research is needed for safety confirmation.

Three drugs change mice's alcohol drinking patterns by affecting GABAA receptors.

Finasteride reduces alcohol withdrawal severity in male mice but increases it in female mice.

The document concludes that sexual and psychiatric side effects from 5-alpha-reductase inhibitors are reported, but more high-quality research is needed to understand how often they occur.

Progesterone and related compounds may help control seizures linked to the menstrual cycle but have limitations that need addressing.

Finasteride use may lead to less alcohol consumption in men with lasting sexual side effects.

PCOS is a complex disorder managed by treating symptoms and requires a team of specialists.

Using 17-hydroxyprogesterone levels to diagnose nonclassic congenital adrenal hyperplasia can result in many incorrect diagnoses.

Finasteride blocks progesterone's effect on absence seizures in rats.

The document concludes that PCOS has a strong genetic component, but more research is needed to fully understand the specific genes involved.

Allopregnanolone is needed for certain brain processing issues caused by D1 dopamine receptor activation.

Progestogens are essential in menopausal hormone therapy to prevent uterine cancer and must be chosen carefully based on individual needs.

Progesterone treatment improved seizures in a woman with menstrual cycle-related epilepsy, but a wrong medication worsened her condition.

A young woman's symptoms suggested PCOS, but tests and surgery confirmed and treated a rare ovarian tumor, resolving her condition.

Male tissue has more cell death than female tissue after ischemia, and some neurosteroids only protect female cells.

Finasteride treats baldness but may cause lasting sexual side effects.

Neuroimaging suggests that treatments targeting brain steroids could help control epilepsy, especially types linked to the menstrual cycle.

Male androgenetic alopecia involves hair follicle miniaturization due to DHT, with potential treatments using inhibitors and blockers.

Longer anogenital distance may indicate a higher chance of having polycystic ovary syndrome, and measuring this distance along with hormone levels could improve diagnosis.

Genetic mutations can affect female sexual development, requiring personalized medical care.

Removing certain brain receptors in mice worsens seizure severity and response to treatment during hormone withdrawal.