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A new genetic mutation in the CDH3 gene causes hair loss and eye problems in young people.

A complex X chromosome rearrangement can increase the risk of multiple autoimmune diseases.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

The baby’s hair loss was due to a rare genetic condition, not treatable by usual methods.

COVID-19 can lead to different skin symptoms and might trigger autoimmune diseases in genetically susceptible people.

Alopecia Areata affects people of all ages worldwide, is likely caused by genetic and environmental factors, and can lead to stress and depression, highlighting the need for treatments that address both physical and mental health.

Early genetic testing and JAK inhibitors can help treat systemic inflammation in SAVI patients.

A Holstein calf in Iran with a severe genetic skin disorder was euthanized due to incurable symptoms.

Vitiligo is often found with other autoimmune diseases, which is important to know to help patients.

Some people with the skin color loss condition, vitiligo, also develop the skin inflammation condition, lichen planus, possibly due to local trauma, sun damage, or genetic factors.

A 45-year-old woman with autoimmune diseases experienced patchy hair loss due to alopecia areata, which has no cure but can be treated, with varying success.

Experts discussed hair care, genetic hair defects, hair loss treatments, nail surgery, lupus treatments, skin infections, and cosmetic allergies.

Genetic testing for EGFR mutations is crucial in similar cases.

Topical Imiquimod may fight vascular tumors by affecting blood vessels or the immune system, low iron might be linked to some hair loss, removing the top skin layer helps vitamin C get in, genetic testing helps diagnose skin conditions, and too much iron could worsen skin inflammation.

Alopecia areata is a common autoimmune disease affecting about 2% of people, causing significant disability and often associated with mental health issues and other autoimmune conditions.

The book explains how excess male hormones can affect various conditions like Polycystic Ovary Syndrome and Cushing's disease.

Different human traits like skin color and hair type vary between populations due to genetic adaptations to the environment.

Female and male AGA are different diseases.

New method finds genetic links between Type 2 Diabetes and Prostate Cancer not seen before.

The document describes previously unreported unique skin changes in a rare genetic disorder called Hereditary mucoepithelial dysplasia.

Male pattern baldness is often genetic and linked to a hormone, with treatments like finasteride and minoxidil being effective for some men.

A rare genetic mutation causes resistance to vitamin D, leading to severe rickets and requiring high doses of calcium and vitamin D for treatment.

Hashimoto thyroiditis is an autoimmune disease that can lead to an underactive thyroid and is treated with medication and sometimes diet changes or surgery.

Certain KIR genes in Indian SLE patients are linked to disease severity and could be biomarkers.

Progeria, a disease that causes early aging, is linked to a gene mutation and helps us understand normal aging.

Lupus is a complex disease that requires personalized treatment because it varies greatly between individuals.

The document concludes that alopecia areata is an autoimmune disease without a definitive cure, but treatments like corticosteroids are commonly used.

Pediatric systemic lupus erythematosus is a severe autoimmune disease in children requiring early diagnosis and comprehensive management.

Tissue-specific variation in mutant load complicates genetic counseling and prenatal diagnosis.

Hormones affect prostate health and disease, with certain hormone imbalances linked to prostate cancer and benign prostatic hyperplasia.