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

There is no clear recommendation for using selenium in cancer patients; it may be beneficial to correct low selenium levels before treatment.

The document suggests treating individuals with nonclassic congenital adrenal hyperplasia who show symptoms, especially those related to excess male hormones.

Keratins are important for skin cell health and their problems can cause diseases.

HIV can cause unusual and severe skin problems that are hard to treat.

People with atopic dermatitis are more likely to develop other skin conditions due to shared genetics and immune pathways.

Runx1 controls fat-related genes important for normal and cancer cell growth, affecting skin and hair cell behavior.

People with myotonic dystrophy type 1 have a higher chance of getting skin tumors, including melanoma.

HPV16 oncogenes disrupt the normal activity of hair follicle stem cells.

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.