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Certain genetic variations in the RAB5B gene are linked to a higher risk of polycystic ovary syndrome in Chinese Han women.

IV cyclophosphamide effectively treated severe lupus nephritis in Indian patients, but longer follow-up is needed.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

Sodium metabisulfite increases sodium channel activity, leading to higher cell excitability and potential damage.

"Coco de mono" seeds cause temporary hair loss due to selenocystathionine.

Lupus can be a rare cause of high calcium levels in the blood.

A gene mutation causes curly hair and hair loss in rats.

Most 46XX CAH patients have female identity, but a few identify as male and may need treatment and surgery.

Diagnosing both systemic lupus and hemoglobinopathy is challenging due to overlapping symptoms.

Mother-in-law's tongue leaf extract at 20% concentration significantly promotes hair growth in male rabbits.

A rare ovarian tumor was successfully treated with surgery and chemotherapy.

SFE is a better extraction method, and the HPTLC method is effective for analyzing wedelolactone in E. alba.

Early recognition and aggressive treatment can significantly improve rare ANA-negative lupus with heart and skin issues.

Gender-specific analysis could improve treatment for childhood systemic lupus erythematosus.

AtCSLD3 and GhCSLD3 genes enhance root growth and cell elongation in plants.

The woman was diagnosed with lichen sclerosus, a rare skin condition, after initial misdiagnosis and ineffective treatments.

Selenium supplements can help improve symptoms and metabolic markers in lupus patients.

A genetic hair protein variant is more common in Japanese people and is inherited.

Cats with abnormal hair had DSG4 gene changes causing hair problems.

Lupus can cause unusual vision problems, so it's important to consider it in such cases.

Somatostatin analogues effectively manage ectopic ACTH syndrome when surgery isn't possible.

A gene variant in KRT71 causes the curly fur in Selkirk Rex cats.

Mice with the 'lanceolate hair' mutation have abnormal hair and skin similar to human Netherton's syndrome.

Anti-SRP myopathy can be linked to systemic lupus erythematosus and may improve with specific treatment.

The drug TGU was ineffective against small cell lung cancer and caused significant bone marrow suppression.

A new mutation in the KRT86 gene causes monilethrix in a Han family.

Errors found in identifying furosemide and finasteride polymorphs due to incomplete data.

The frizzy mouse and hairless rat mutations are due to changes in the Prss8 gene.