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Hemolytic jaundice, also known as prehepatic jaundice, is a type of jaundice arising from hemolysis or excessive destruction of red blood cells, when the byproduct bilirubin is not excreted by the hepatic cells quickly enough. [1]
Jaundice, also known as icterus, is a yellowish or greenish pigmentation of the skin and sclera due to high bilirubin levels. [3] [6] Jaundice in adults is typically a sign indicating the presence of underlying diseases involving abnormal heme metabolism, liver dysfunction, or biliary-tract obstruction. [7]
Physical examination reviews clinical symptoms like degree of jaundice, vital signs and sensations of pain, further followed by urine tests, blood analysis and imaging. [3] [4] The degree of yellowish staining of the conjunctiva and skin in jaundice is proportional to hyperbilirubinemia to some extent. [6]
Symptoms: Usually none, still, abdominal pain, nausea, tired and weak feeling, slight jaundice may present [1] Complications: Usually none [1] Causes: Genetic [1] Differential diagnosis: Crigler–Najjar syndrome, Rotor syndrome, Dubin–Johnson syndrome [2] Treatment: None typically needed [1] Frequency ~5% [3]
Rotor syndrome (also known as Rotor type hyperbilirubinemia) [2] is a rare cause of mixed direct (conjugated) and indirect (unconjugated) hyperbilirubinemia, relatively benign, autosomal recessive [3] bilirubin disorder characterized by non-hemolytic jaundice due to the chronic elevation of predominantly conjugated bilirubin.
Around 80 to 99% of people with Dubin–Johnson syndrome have jaundice, [3] [4] abnormal urinary color, biliary tract abnormality, and conjugated bilirubinemia. [4] Around 30 to 79% of people with the disorder have abnormality of the gastric mucosa. [4] Other rare symptoms include fever and fatigue. [3]
Being 45 or older Health conditions like high blood pressure, high cholesterol , metabolic syndrome, or sleep apnea Having a medical history of gestational diabetes, heart disease, or stroke
Hereditary hyperbilirubinemia refers to a group of conditions where levels of bilirubin, a byproduct of red blood cell metabolism, are elevated in the blood due to a genetic cause. [1] Various mutations of enzymes in the liver cells, which breakdown bilirubin, cause varying elevated levels of bilirubin in the blood. [ 2 ]