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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Identifiers and source
- Literature Corpus work
- acf80ff6-7b59-5658-8dc6-ac4a5538ba3f
- DOI
- 10.21203/rs.3.rs-5146957/v1
