Article

Hereditary Spherocytosis Caused by a Novel Compound Heterozygous Mutation of the SPTA1 Gene and Autoimmune Hepatitis in a Pediatric Patient

2021-11-01

Abstract excerpt

<title>Abstract</title> <p><bold>Objective: </bold>Patients suffering from both hereditary spherocytosis (HS) and autoimmune hepatitis (AIH) are very rare. We analyzed the clinical and genetic characteristics of a seven-year-old girl with yellow sclerae and abnormal liver function tests, but no further symptoms. <bold>Methods: </bold>Blood samples were collected from the proband, her parents, and her paternal gra...

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Literature Corpus work: 3e733b65-1fa7-52e5-a974-506ad9b17bb5
DOI: 10.21203/rs.3.rs-1023423/v1

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