Hereditary spherocytosis is a genetic condition affecting the red blood cells, characterized by destruction of the red blood cells in the spleen, yellow discoloration of the skin, and enlargement of the spleen. The cause of the condition is a genetic defect that is transferred from parents to children. The diagnosis of hereditary spherocytosis is made on the basis of peripheral blood smear examination, red cell fragility test, etc. The treatment of the condition includes blood transfusion, folic acid supplements, and partial or complete removal of the spleen.
Hi, Welcome to icliniq.com. Yes, it is a disorder that may cause an unstable RBC (red blood cells) membrane, leading to the production of spherical-shaped RBC.
Hello, Welcome to icliniq.com. Your spleen is enlarged in size (attachment removed to protect patient identity). The liver appears normal in size, and the echotexture looks normal.
Hello, Welcome to icliniq.com. Thank you for your query. I read your query and understand your concern.
Hello, Welcome to icliniq.com. I have gone through your laboratory reports (attachment removed to protect patient identity) and they are consistent with the diagnosis made by your doctor.
Hello, Welcome to icliniq.com. It appears that hereditary spherocytosis is responsible for the problem. It results in an increased breakdown of RBC or red blood cells, which results in hemolytic anemia. Jaundice is due to hereditary spherocytosis, and jaundice is causing itching.
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