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Article

Neonatal Hereditary Spherocytosis: A Case Report

2024-12-04

Abstract excerpt

<title>Abstract</title> <p>Background: hereditary spherocytosis is a genetic disorder affecting red blood cell membranes, leading to increased destruction and haemolysis. In neonates, it ranges from asymptomatic to severe cases with anaemia, jaundice, and spleen issues. Early diagnosis through clinical, laboratory, and genetic tests is vital for prognosis. This clinical case is presented due to the rarity of neon...

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Literature Corpus work
acf80ff6-7b59-5658-8dc6-ac4a5538ba3f
DOI
10.21203/rs.3.rs-5146957/v1
Open publication

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Neonatal Hereditary Spherocytosis: A Case ReportDOI 10.21203/rs.3.rs-5146957/v1
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