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The study found that heart disease is common in people with PCOS and that being overweight is a major risk factor; lifestyle changes and medication are important for management.

A girl with a rare genetic disorder had a unique bone condition, highlighting the need for careful diagnosis and suggesting the disorder might be more common than thought.

The absence of functional sebaceous glands causes hair follicle destruction and scarring alopecia.

Genetic variations greatly affect individual metabolism and can impact health and disease risk.

The conclusion is that genetic testing is important for diagnosing and treating various genetic hair disorders.

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

Genes and epigenetic changes are important in the development of Polycystic Ovary Syndrome.

Hair loss in women can be caused by genetics, menopause, certain health conditions, and emotional stress, and it often results in thinner hair and a changing hairline.

HLA-DRB5 and other genes may be linked to alopecia universalis.

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

Researchers found genes that may explain why some pigs grow winter hair, which could help breed cold-resistant pigs.

Scalp melanoma, a deadly skin cancer, is often found late due to its hard-to-see location, especially in older men. Early detection, possible treatments, and the role of hairdressers in spotting it early are discussed. More research is needed to improve detection and treatment.

Men with androgenetic alopecia and hypertension may experience more severe COVID-19.

CXXC5 is a protein that controls cell growth and healing processes, and changes in its activity can lead to diseases like cancer and hair loss.

New treatments for non-small cell lung cancer are being tested, with some already in use, focusing on immune response and targeting cancer cells, but side effects vary.

Early diagnosis and a combination of treatments, including minoxidil and finasteride, are recommended for managing hair loss in India.

Female cuckoo color differences are linked to their unique genes and help avoid male harassment.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

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

Actinic keratosis can lead to skin cancer, is more common in fair-skinned people, and can be reduced with sunscreen and treated effectively.

Certain gene variations are linked to better memory in healthy Chinese women.

Chromosomal changes, including those in the WRN gene and rDNA, may significantly contribute to aging.

Keratin genes change gradually during skin cell development and should be used carefully as biomarkers.

Doctors should consider SLE in males even if antinuclear antibody tests are negative.

Mutant mice help researchers understand hair growth and related genetic factors.

New markers and pathways have been found in skin tumors, helping better understand and diagnose them.

Certain genetic variants in the androgen receptor are linked to higher PSA levels, potentially affecting prostate cancer screening outcomes.

Certain gene variations might be linked to severe acne in women but not in men.

An 11-year-old Greek girl was diagnosed with a rare genetic disorder, highlighting the importance of genetic testing and family history.

Most children with a common hemochromatosis genotype had elevated iron levels but no severe symptoms.