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A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

New treatments and diagnostic methods for various animal skin conditions showed promising results.

Athletes need effective management of skin disorders for their performance and well-being.

Pregnant women with Systemic Lupus Erythematosus have a higher risk of blood clotting problems.

The conclusion is that genetic changes in the glucocorticoid receptor can lead to conditions affecting stress response, immunity, and metabolism, requiring personalized treatment.

Late diagnosis of congenital adrenal hyperplasia can greatly affect physical development, gender identity, and sexual health.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

A new mutation in the human glucocorticoid receptor reduces its function and causes resistance to glucocorticoids.

High levels of TNF-α may contribute to obesity and insulin resistance in PCOS, but not due to the C850T genetic variation.

Amenorrhea is relatively rare and initial testing should check FSH, TSH, and prolactin levels.

MSC-Exos can aid organ development and offer therapeutic benefits for various conditions.

Lower PPARγ levels and specific gene variations are linked to more severe Frontal Fibrosing Alopecia.

The document concludes that accurate diagnosis of male and female gonadal disorders is crucial for effective treatment and better patient outcomes.

The document concludes that identifying the cause of amenorrhea is crucial for proper treatment.

Amenorrhea, or the absence of periods, should be evaluated by age 15 or within five years of early breast development, and is most commonly caused by conditions like polycystic ovary syndrome and hypothalamic amenorrhea.

Amenorrhea is when a woman doesn't have periods, with primary amenorrhea starting by age 15 or within five years of breast development, and secondary amenorrhea when periods stop for three months. It affects 3-4% of women not pregnant, breastfeeding, or in menopause, mainly due to polycystic ovary syndrome, hypothalamic amenorrhea, hyperprolactinemia, and ovarian failure.

Hidradenitis suppurativa is caused by genetic factors, inflammation, bacteria, hormones, and lifestyle factors like obesity and smoking.

Acne is significantly influenced by genetics, and understanding its genetic basis could lead to better, targeted treatments.

Natural products in cosmetics are beneficial for skin and hair care with low toxicity.

The document concludes that more research is needed to understand hair loss in men and to find new treatments.

A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

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

Genetic research has advanced our understanding of skin diseases, but complex conditions require an integrative approach for deeper insight.

People with atopic dermatitis have different skin bacteria, and targeting these bacteria might help treat the condition.

Newborn screening and gene therapy are expected to improve outcomes for Omenn syndrome patients.

Oral contraceptives provide various health benefits beyond birth control, including managing menstrual issues, skin conditions, pain, and reducing the risk of certain cancers.

The nanoemulsion with garlic oil, apple cider vinegar, and minoxidil could effectively treat alopecia areata.

Adult acne is often related to hormonal disorders, especially in women, and may need long-term treatment involving specialists.

Pumpkin Seed Oil in niosomes may help treat hair loss and improve hair growth.

Some drugs may help treat both COVID-19 and radiation injury.