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The protein CTCF is essential for skin development, maintaining hair follicles, and preventing inflammation.

Cross-section trichometry is an accurate method to measure hair loss and growth.

Congenital Adrenal Hyperplasia is a genetic disorder with two forms, causing symptoms like early puberty and severe acne, but can be identified through screening and treated with glucocorticoids.

Obesity worsens PCOS symptoms, and PCOS may lead to more weight gain; managing both requires a holistic approach that includes mental health.

People with PCOS, especially if obese, often have NAFLD, linked to obesity, insulin resistance, and high androgen levels.

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

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

Non-classic congenital adrenal hyperplasia is a common disorder causing symptoms like acne and infertility, and it's managed based on symptoms, not just test results. Treatment can improve fertility and reduce miscarriage risk.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

The VEGF +405G allele may increase the risk of PCOS in South Indian women.

Sex hormones like estrogen and testosterone may affect COVID-19 severity differently in men and women, potentially influencing prevention and treatment strategies.

New genetic insights have improved understanding of hair loss, leading to a new test and treatments, but more research is needed on the test and laser comb effectiveness.

The G60S Connexin43 mutation causes hair growth issues and poor hair quality in mice, similar to human ODDD patients.

Researchers found two genes that may explain why some Casertana pigs don't have hair.

A woman with acromegaloidism and normal growth hormone levels had a rare X-Tetrasomy, suggesting a need to study X-chromosome genes for their role in growth and facial development.

We need better ways to test and understand SARMs to make safer and more effective treatments.

Genetic variants at 20p11 increase baldness risk in Chinese Han people.

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

Birt–Hogg–Dubé syndrome is a rare genetic condition causing skin lesions, lung cysts, and a higher chance of kidney cancer.

Most hair loss in children is caused by a few common conditions and is easy to diagnose, but rare types require careful evaluation.

Favus, a rare fungal infection, has reappeared in Japan.

A new therapy for a skin blistering condition has not been developed yet.

Gluconolactone products can significantly reduce skin scaling in golden retrievers with ARCI.

The study found two new mutations in a Chinese patient with severe biotinidase deficiency.

A man with myotonic dystrophy type 1 had 28 skin cancers, suggesting a link between the disease and skin cancer, emphasizing the need for sun protection and regular skin checks.

New genetic mutations causing hair loss were found in a Chinese family.

The conclusion is that differentiating wound types in RDEB patients is important for clinical trials and understanding the disease.

Molecular diagnostics help identify genetic defects causing endocrine diseases, improving diagnosis and treatment options.

High-dose finasteride may help treat glioblastoma but needs localized delivery for effectiveness.

Woodhouse-Sakati syndrome can cause writer's cramp and other varied symptoms, highlighting the importance of genetic testing for diagnosis.