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MendelVar is a tool that helps identify important genes by combining GWAS data with Mendelian disease information.

A Korean boy's skin and digestive symptoms were caused by a rare genetic disorder that affects zinc absorption, and he got better with zinc supplements.

Gastric bypass surgery improved a woman's hormonal disorder without the need for medication.

Zinc is crucial for skin health and treating various skin disorders.

Canine hair follicles have stem cells similar to human hair follicles, useful for studying hair disorders.

A certain mutation in the fetal alpha 5-reductase gene is linked to a higher risk of late miscarriage.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

PCOS causes infertility mainly due to hormonal imbalances, insulin resistance, and chronic inflammation.

A special gene region controls the re-emergence of a primitive wool type in Merino sheep, improving their wool yield and adaptability.

Polycystic ovary syndrome causes high male hormone levels, leading to symptoms like excess hair, acne, and fertility problems.

A girl with skin rashes and low zinc levels improved with zinc supplements and had new gene mutations linked to her condition.

Eating a Mediterranean diet and taking certain supplements may improve symptoms of PCOS.

PCOS is a complex condition in women that can lead to health issues, and lifestyle changes are the best management approach.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

A pregnant woman with Werner's syndrome died during childbirth, but her baby survived and did not have the syndrome.

Hair loss in Androgenetic Alopecia is caused by genetics, aging, and lifestyle, leading to hair follicle shrinkage and related health risks.

Certain genes may influence hair loss differently in men and women.

Testosterone's effects on COVID-19 are unclear and need more research.

Type 1 diabetes often occurs with other autoimmune diseases, and personalized treatment based on genetics can improve outcomes.

A gene mutation in Lama3 is linked to a common type of hair loss.

Certain surgical methods are better than routine incision for hidradenitis suppurativa, topical clindamycin and acitretin are effective treatments, men with HS have a risk of skin cancer, HS patients are more likely to die from heart problems, and specific genetic markers are linked to treatment response.

Alopecia areata patients, especially women with nail issues or atopic diseases, are at higher risk for other autoimmune diseases.

Early diagnosis of Trichorhinophalangeal syndrome type 1 is crucial for treatment and was achieved through clinical examination and family history.

A patient with a scalp condition and benign skin tumor experienced hair loss and did not improve with treatment, choosing not to have surgery despite a small cancer risk.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

Hair follicle studies suggest that maintaining telomere length could help treat hair loss and graying, but it's uncertain if mouse results apply to humans.

Obesity leads to physical, metabolic, reproductive issues, higher healthcare costs, and mental health problems.

The document concludes that inflammation markers can be used in diabetes, vitamin D3 affects immune pathways, hyperthyroidism changes hormone levels, androgen levels help diagnose Adrenocortical Carcinoma, erectile dysfunction is linked to diabetes, hypogonadism is common in HIV-infected males, and hormones can be biomarkers for various conditions.

Androgenetic alopecia in men is genetic and linked to health issues like obesity and heart disease, with treatments including minoxidil, finasteride, and hair transplants.

HOXC13 is essential for hair and nail development by regulating Foxn1.