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Liver Involvement in Patients with Rare IMBOAT7/I Variants and Intellectual Disability: A Case Report and Literature Review
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Liver Involvement in Patients with Rare IMBOAT7/I Variants and Intellectual Disability: A Case Report and Literature Review
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Journal Article
Liver Involvement in Patients with Rare IMBOAT7/I Variants and Intellectual Disability: A Case Report and Literature Review
2023
Overview
The membrane-bound O-acyltransferase domain-containing 7 (MBOAT7) protein is an acyltransferase catalyzing arachidonic acid incorporation into lysophosphatidylinositol. Patients with rare, biallelic loss-of-function variants of the MBOAT7 gene display intellectual disability with neurodevelopmental defects. The rs641738 inherited variant associated with reduced hepatic MBOAT7 expression has been linked to steatotic liver disease susceptibility. However, the impact of biallelic loss-of-function MBOAT7 variants on liver disease is not known. We report on a 2-year-old girl with MBOAT7-related intellectual disability and steatotic liver disease, confirming that MBOAT7 loss-of-function predisposes to liver disease.
Publisher
MDPI AG
Subject
