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Liver Transplantation for Zellweger Syndrome

Overview
Specialty Pediatrics
Date 2023 Dec 20
PMID 38117438
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Abstract

Zellweger syndrome or cerebrohepatorenal syndrome is a rare, multisystem disorder occurring due to defect in metabolic pathway within the peroxisomes. Cirrhosis with portal hypertension is an important presentation of these patients. Given its progressive, multisystem nature, the role of liver transplantation (LT) in Zellweger syndrome remains undefined and controversial. An 11-y-old boy diagnosed with Zellweger syndrome presented to the authors with decompensated cirrhosis along with bilateral proptosis. After a meticulous evaluation, he was offered an ABO incompatible liver transplantation with his mother being the donor. He had an uneventful post operative period. After a follow up of 24 mo, he has normal graft function, normal cognition along with resolution of proptosis. Therefore, in a group of carefully selected patients with Zellweger syndrome, a liver transplantation can be offered successfully with an excellent prognosis.

References
1.
Klouwer F, Berendse K, Ferdinandusse S, Wanders R, Engelen M, Poll-The B . Zellweger spectrum disorders: clinical overview and management approach. Orphanet J Rare Dis. 2015; 10:151. PMC: 4666198. DOI: 10.1186/s13023-015-0368-9. View

2.
Demaret T, Varma S, Stephenne X, Smets F, Scheers I, Wanders R . Living-donor liver transplantation for mild Zellweger spectrum disorder: Up to 17 years follow-up. Pediatr Transplant. 2018; 22(3):e13112. DOI: 10.1111/petr.13112. View

3.
Schutgens R, Wanders R, Heymans H, Schram A, Tager J, Schrakamp G . Zellweger syndrome: biochemical procedures in diagnosis, prevention and treatment. J Inherit Metab Dis. 1987; 10 Suppl 1:33-45. DOI: 10.1007/BF01812845. View

4.
Steinberg S, Chen L, Wei L, Moser A, Moser H, Cutting G . The PEX Gene Screen: molecular diagnosis of peroxisome biogenesis disorders in the Zellweger syndrome spectrum. Mol Genet Metab. 2004; 83(3):252-63. DOI: 10.1016/j.ymgme.2004.08.008. View