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Skin and hair changes in horses can indicate serious diseases, and recognizing these signs is important for treatment and management.

Dermoscopy greatly improves melanoma diagnosis and reduces unneeded surgeries.

There is no cure for myotonic dystrophy type 1, so treatment focuses on managing symptoms and complications.

APS-1 in Italy shows diverse AIRE mutations and various autoimmune issues.

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

The document reports findings on genetic research, including ethical concerns about genome editing, improved diagnosis of mitochondrial mutations, solving inherited eye diseases, confirming gene roles in epilepsy, linking a gene to aneurysms, and identifying genes associated with age-related macular degeneration.

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.

Antioxidants can help improve hair growth in people with alopecia areata.

Lupus treatment requires a combination of drugs and therapies, with research needed for new options.

Foreign-body granuloma may be a marker for late-stage Lichen Planopilaris and should be considered in diagnosis.

The 2006 editorial concluded that immunotherapy was advancing with new drugs, focusing on specific biological therapies and convenient oral treatments, and highlighted the importance of partnerships and new regulations in the field.

The conclusion is that formalizing how past decisions influence current health technology assessments could improve the credibility and defense of coverage decisions.

Genetic discoveries are leading to new treatments for alopecia areata.

Exosomes could be effective for improving skin health and treating skin diseases.

Genetic variants in PDE6H and LPAR6 cause vision impairment and hair loss in two Pakistani brothers.

Men with more severe hair loss had a lower risk of schizophrenia, but hair loss and testosterone levels were not linked.

Early detection and intensive treatment of diseases caused by Staphylococcus aureus toxins are crucial for reducing severe health effects.

Trichoscopy is essential for early detection and monitoring of female-pattern hair loss.

Researchers found that certain RNA circles in the brain are linked to disease risk, but their exact role in disease is still unknown.

Early detection and treatment of folliculitis keloidalis can prevent disease progression.

Ultrasound shows 80% of Hidradenitis Suppurativa patients have abnormal hair tracts that may worsen the condition.

The patient was diagnosed with celiac disease after a long delay, showing the need for better awareness and earlier detection.

Girls with Pilonidal Disease are more likely to have Polycystic Ovarian Syndrome, and treating PCOS may reduce the need for PD intervention.

Many people in Saudi Arabia lack awareness of thyroid disease risk factors and symptoms, highlighting the need for better health education.

Flow cytometry was effective in diagnosing metastatic breast cancer in a bone marrow sample.

Higher levels of certain immune cells and proteins are linked to more severe lupus symptoms.

The virus linked to a rare disease was found in a patient's blood and urine before skin symptoms appeared.

A woman with Castleman's disease died from respiratory failure due to bronchiolitis obliterans.

Trichoscopy is useful for detecting and monitoring androgenetic alopecia.

Androgenetic alopecia is linked to a higher risk of coronary heart disease due to certain genetic factors and high homocysteine levels.