Night sweats
Possible conditions
Tuberculous Arthritis — 6 Genes and 7 Biomarkers to Track
If you or someone close to you has been diagnosed with tuberculous arthritis — or is being investigated for it — you already know how disorienting the process can feel. This is not a common diagnosis in many countries, and yet it remains a significant cause of joint destruction worldwide, particularly in regions where tuberculosis is endemic or in individuals with compromised immunity.
Brucellosis Genes and Biomarkers – 7 Genes and 7 Biomarkers to Track
Brucellosis is one of those conditions where standard treatment — a weeks-long course of dual antibiotics — does most of the heavy lifting, yet a surprising number of people still deal with lingering fatigue, joint pain, sweating episodes, and relapse long after their physician has declared them cured.
Schnitzler Syndrome – 7 Biomarkers and 5 Genes to Track
Living with Schnitzler syndrome means navigating a condition that most people — including many physicians — have never encountered. The hallmark combination of chronic urticarial rash, recurring fever, and deep bone pain, accompanied by a monoclonal protein circulating in the blood, is distinctive once you know what to look for.
Multicentric Castleman Disease Genes Biomarkers
Multicentric Castleman Disease sits in a strange corner of medicine — serious enough to be life-altering, rare enough to be regularly missed, and complex enough that even experienced hematologists sometimes spend months before arriving at the right diagnosis.
Kikuchi-Fujimoto Disease Genes & Biomarkers: 5 Genes And 6 Biomarkers To Track
Kikuchi-Fujimoto disease tends to arrive without warning. One week you notice a swollen, tender lymph node on the side of your neck. Then comes the fever that refuses to break, the night sweats soaking through your clothes, a fatigue so heavy that ordinary days become difficult.
Cartilage-Hair Hypoplasia: 5 Genes and 6 Biomarkers to Track
Living with cartilage-hair hypoplasia, or caring for someone who does, means navigating a condition that most doctors encounter once in a career, if ever. CHH is a rare autosomal recessive skeletal dysplasia caused by mutations in the RMRP gene, which encodes the RNA subunit of the RNase MRP enzyme.
Rosai-Dorfman Disease: 4 Genes and 7 Biomarkers to Track
If you're reading this, you're probably holding a pathology report with words like "emperipolesis," "S100-positive," or "non-Langerhans cell histiocytosis," and trying to figure out what any of it means for you or someone you love.
Popliteal Lymphadenopathy: 7 Biomarkers and 4 Genes to Track
Finding a firm, swollen lump behind the knee is unsettling in a specific way. It's not a place people expect a lymph node to announce itself, and a quick search tends to produce either reassuring dismissals or worst-case scenarios, with very little in between.