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Unique Mutation in SP110 Resulting in Hepatic Veno-Occlusive Disease with Immunodeficiency.

Authors :
Hamdoun O
Al Mulla A
Al Zaabi S
Shendi H
Al Ghamdi S
Hertecant J
Al-Shibli A
Source :
Case reports in pediatrics [Case Rep Pediatr] 2020 Jan 10; Vol. 2020, pp. 3460631. Date of Electronic Publication: 2020 Jan 10 (Print Publication: 2020).
Publication Year :
2020

Abstract

Familial hepatic veno-occlusive disease with immunodeficiency (VODI, OMIM: 235550) is a rare form of combined immune deficiency (CID) that presents in the first few months of life with failure to thrive, recurrent infections, opportunistic infections along with liver impairment. Herein, we are describing a Pakistani patient with a homozygous novel variant in the SP110 gene, presenting with classical phenotypic manifestations of VODI. He presented at the age of 3 months with opportunistic infections and later developed liver failure. Conclusion . Hepatic veno-occlusive disease with immunodeficiency is a rare cause of immunodeficiency, and this is the first case report from the Middle East in a patient of Pakistani origin. It is important to have a high suspicion for this disease, in patients presenting early life with a picture of CID and deranged liver function, as the earlier the diagnosis and treatment, the better the prognosis.<br />Competing Interests: The authors declare that they have no conflicts of interest.<br /> (Copyright © 2020 Osama Hamdoun et al.)

Details

Language :
English
ISSN :
2090-6803
Volume :
2020
Database :
MEDLINE
Journal :
Case reports in pediatrics
Publication Type :
Report
Accession number :
32395362
Full Text :
https://doi.org/10.1155/2020/3460631