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PFS and PSSD are similar conditions with persistent sexual dysfunction after stopping medication.

Finasteride may help reduce symptoms in male Tourette syndrome patients.

Weight loss and metformin don't significantly change vaspin levels in women with PCOS.

A male with aromatase deficiency improved bone health with estradiol treatment.

The document describes a woman with familial Parkinson's disease due to a genetic mutation, showing severe symptoms and poor response to treatment, and suggests finasteride may help reduce symptoms in Tourette syndrome.

The research suggests that the ZP4 gene is linked to egg development in women with PCOS but requires more study to understand its role in infertility.

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

Finasteride significantly reduced tics and obsessive-compulsive symptoms in patients with Tourette syndrome.

CAH is a genetic disorder affecting cortisol production and causing hormonal imbalances, with treatment and diagnosis varying by form and symptoms.

People with myotonic dystrophy type 1 tend to develop basal cell carcinoma at a younger age but not more frequently than others.

THAP1 gene changes do not affect DYT1 dystonia; finasteride may help reduce tics and OCD in Tourette syndrome.

Low birthweight and rapid weight gain after birth may increase the risk of developing polycystic ovary syndrome.

People with Myotonic Dystrophy type 1 are more likely to have certain skin conditions, but not more likely to get skin cancer.

The document concludes that periocular hair disorders have various causes and treatments, and proper evaluation by specialists is important for management and prognosis.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

Finasteride significantly reduced tics and obsessive-compulsive symptoms in Tourette syndrome patients.

Finasteride may help reduce tic severity in male Tourette syndrome patients.

A woman with acne and baldness was found to have a rare ovarian condition but successfully had a child through fertility treatment.

A woman's unique dementia was misdiagnosed, a genetic mutation increases Parkinson's risk with age, and finasteride may help with Tourette syndrome.

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

Alopecia Areata is an autoimmune condition causing hair loss with no cure and treatments that often don't work well.

Exposure to too much androgen before birth might cause polycystic ovary syndrome later in life.

High levels of male hormones, insulin resistance, and obesity are closely linked and worsen polycystic ovary syndrome, but more research is needed to improve treatments.

Guidelines for diagnosing common hair loss include detailed history, clinical examination, and various diagnostic techniques.

GABRA2 gene variations impact alcohol response, and hair loss medication finasteride reduces some effects.

A WNT10A gene mutation leads to ectodermal dysplasia by disrupting cell growth and differentiation.

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

COVID-19 can cause various skin lesions, which may result from the virus and immune response, and are not directly linked to illness severity.

Nonclassic adrenal hyperplasia is a genetic condition that can cause early puberty and fertility problems, treated with specific steroids.

DHT, a testosterone byproduct, causes male pattern baldness.