Treatment and Diagnosis

Diagnosis Reviewing Personal and Family Background The process begins when a healthcare provider collects detailed information about the individual’s health and family history. Since people with…

Diagnosis To identify primary ovarian insufficiency, doctors begin by gathering information about symptoms, such as irregular menstrual periods, early menopause, or trouble becoming pregnant. They ask…

Diagnosis Doctors diagnose Wilson’s disease by looking at symptoms and using several tests. This genetic condition can show up with many signs that may look like…

Diagnosis Doctors use several methods to find out if someone has small vessel disease. They often start by talking to the patient about symptoms like chest…

Diagnosis Doctors may not notice triple X syndrome right away, as many females have no clear signs or only mild symptoms. Some people receive a diagnosis…

Diagnosis A healthcare professional starts with a physical examination. They look for common signs, such as skin changes and abdominal discomfort. Observing symptoms helps decide which…

Reye syndrome is a rare and serious condition that mostly affects children and teens. It can develop quickly, often after a viral infection such as the…

Treatment Clinicians diagnose glomerulonephritis using a mix of tools to check for kidney disease and understand its cause and severity. A health provider reviews a person’s…

Diagnosis Blood and Urine Analysis Doctors often start by ordering several laboratory tests when granulomatosis with polyangiitis (GPA) is suspected. A complete blood count checks if…

Diagnosis Evaluating with the Coma Scale Medical teams use the Glasgow Coma Scale to measure how severe a brain injury is. They check if a person…