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The NUDT15 gene variant causes severe side effects from azathioprine in some Indian patients.

The document concludes that patients with skin of color need specialized dermatological care and education to manage unique skin conditions effectively.

Not having enough or having too much of the protein Grainyhead-like 3 leads to various developmental problems.

Nutrease powder, a high-protein, low-carb supplement, can help manage Polycystic Ovary Syndrome symptoms, regulate periods, improve ovulation, and restore fertility.

Different connective tissue disorders have unique symptoms and treatments, with varying outcomes and often require ongoing care from a specialist.

A man with a rare skin condition and a new gene mutation developed high calcium levels due to his treatment.

The document concludes that Borrelia afzelii causes a skin condition in France, a gene is linked to hair loss in Caucasian women, and various genetic mutations affect skin diseases.

Older adults have a high rate of skin cancers like basal cell carcinoma and melanoma, mainly due to UV exposure and age.

Diagnosing hyperandrogenism in women is complex and requires accurate testing methods and consideration of SHBG levels.

The UD-PrOZA program successfully diagnosed 18% of adult patients with rare diseases, often using genetic testing.

A woman developed Cushing syndrome and adrenal insufficiency from using fluticasone and ritonavir together.

Middle Eastern patients with epidermolysis bullosa show specific genetic mutations linked to different types of the disease.

Keratosis pilaris is often linked to genetic mutations and causes skin and hair abnormalities, regardless of those mutations.

Calcineurin inhibitors, used in kidney transplants, can cause a wide range of side effects including kidney damage and other health issues.

Dihydrotestosterone makes arteries stiffer in female mice by reducing estrogen receptor expression.

The review shows that skin symptoms like chronic fungal infections, hair loss, and skin depigmentation are key for early detection and management of APECED.

Men and women respond differently to drugs for COVID-19, high cholesterol, and diabetes, which suggests a need for personalized treatments.

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.

A woman with childhood growth hormone deficiency had multiple hormone deficiencies and developed serious lung and kidney problems later in life.

Hormonal imbalances may play a role in frontal fibrosing alopecia, and antiandrogenic drugs combined with steroids are currently the most effective treatment.

4-O-methylhonokiol from Magnolia officinalis significantly promotes hair growth.

The conclusion is that PCOS is caused by ovarian sensitivity to hormones and disrupted hormone control, possibly due to ovarian factors, and more research is needed.

The research suggests that the global distribution of PCOS is likely due to historical human migration and that genes affecting PCOS may have different impacts on males and females.

Hepatitis C virus can cause skin diseases and dermatologists play a crucial role in identifying these conditions.

Hormones and genes affect hair growth and male baldness.

Female mice with disrupted 5α-reductase 1 had significant metabolic issues, including stress response problems, insulin resistance, liver fat buildup, and obesity.

New genes linked to ichthyosis were found, but there's still no cure; treatment options are improving.

The E2 protein affects gene activity in hair follicles of mice.

Early treatment of PCOS in teens is crucial to prevent long-term health issues like diabetes and heart disease.

A child with skin and tooth symptoms was found to have a genetic mutation causing cardiocutaneous syndrome, leading to heart problems.