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A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

The mutant HR bmh protein mis-localizes in cells, affecting skin and hair development.

People with rheumatoid arthritis have a higher risk of developing alopecia areata.

FLCN helps control iron levels in cells.

R-Spondin-1 is important for skin health and could help diagnose and treat various skin conditions.

Rheumatology clinics should always provide preconception counseling for women on DMARDs.

Patients with RASopathies have a higher risk of autoimmune disorders and should be routinely screened.

Ruxolitinib significantly improves multiple autoimmune conditions in APS-1 patients.

A rare EGFR mutation in newborns leads to severe health issues and early death.

Matriptase-2 helps control iron levels by suppressing hepcidin, and its deficiency can cause iron-deficiency anemia.

A new genetic change in the keratin 10 gene caused a skin condition called ichthyosis hystrix in a father and his daughter.

A new compound from Royoporus badius activates immune cells and induces inflammatory responses.

Pregnancy can trigger severe rosacea, which may be treated with antibiotics and steroids, but there's no clear treatment guideline.

A patient with Rothmund-Thomson syndrome showed skin changes, hair loss, and dental defects but no cataracts or skeletal issues.

Live vaccines can be safely given to infants with a FOXN1 variant if their immune function improves over time.

Patients with mycosis fungoides have a higher risk of heart disease.

The A allele of the C2 gene increases the risk of lupus, while the G allele may protect against it.

Hereditary factors cause hair loss in mice by affecting skin and hair follicle structure.

Rothmund-Thomson syndrome causes skin changes, hair loss, and slightly high lysine and cystine in urine.

Reticulocyte hemoglobin content is the best indicator of iron deficiency causing hair loss in women.

Women with idiopathic hirsutism and PCOS have higher RBP4 levels, and PCOS is linked to greater insulin resistance; weight management may help both conditions.

Blocking IL-17 can reduce joint inflammation in Ross River Virus infections.

The study suggests that people with rosacea are more likely to have chronic rhinosinusitis.

A new genetic mutation in the TRPS1 gene causes Trichorhinophalangeal Syndrome, leading to specific hair, dental, and bone issues.

Lack of KSR1 stops certain skin tumors in mice.

The conclusion is that certain genetic factors and blood types may affect COVID-19 severity, but changes in ACE2 and TMPRSS2 genes are not clearly linked to it.

A rare skin condition usually found near the eyes was found on a farmer's scalp.

Rb-bFGF improves hair transplant results and patient satisfaction with fewer complications.