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A specific gene variant is linked to severe insulin resistance and hormone imbalance in a teenage girl.

Intramuscular injection of 131I is a safe and effective way to induce hypothyroidism in rats without harming muscle tissue.

Higher levels of MIG and IP-10 may help diagnose and monitor Alopecia Areata.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

A new mutation in the HJV gene was found in a young woman with juvenile hemochromatosis, causing unusual symptoms like secondary hypothyroidism.

The InCISE score is a promising tool for assessing wound healing in head and neck surgery but needs more research for broader use.

A young patient with unusual insulin resistance and high testosterone levels had a rare INSR gene mutation.

Myo-inositol and D-chiro-inositol improve hormonal and physical symptoms in teenage girls with PCOS.

An 8-year-old girl developed a rare skin condition in a linear pattern on one side of her body after a lung infection, which improved with treatment.

Serum IMA levels may be linked to premature hair graying and erectile dysfunction.

A boy with Oculodentodigital syndrome had a unique GJA1 gene mutation causing his symptoms.

Safusidenib erbumine shows promise as a treatment for certain brain tumors, but mild side effects like hair loss need attention.

The new device improves surgical accuracy by using a special dye and camera to see inside tissues.

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

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Early diagnosis and multidisciplinary care, including orthopedic surgery, can prevent long-term disability in IFAP syndrome.

New imaging technology can show up to 40 different markers in hair loss tissue, helping to understand hair disease better.

Anti-MND antibodies are present in various diseases, not just PBC, and their levels don't correlate with disease activity or skin symptoms.

Targeting Hedgehog signaling may help treat ligamentum flavum fibrosis.

Single-dose parenteral iron is safe and effective for children with inflammatory bowel disease and iron-deficiency anemia.

Patients with autoimmune blistering diseases experience a reduced quality of life, with the need for better measurement tools, especially for those with mucous membrane pemphigoid.

A mutation in the SREBF1 gene causes both hereditary mucoepithelial dysplasia and IFAP syndrome, which are related conditions.

An 8-year-old Saudi boy was diagnosed with a rare genetic disorder causing hair loss, skin issues, and light sensitivity.

Shock can be an early sign of Autoimmune Polyendocrine Syndrome Type II.

Careful monitoring is crucial to prevent JC virus reactivation in lupus patients treated with rituximab.

International medical graduates outperformed U.S. graduates on an internal medicine exam.

Myo-inositol improves fertility and metabolic health in PCOS with fewer side effects than metformin.

Excluding alopecia and mucous membrane components from the CLASI-A score reduces its effectiveness in capturing important disease activity.

Platelet-rich plasma shows promise in reducing pain for bladder pain syndrome.