Author(s): da Costa, RQ ; Laranjeira, F ; Ribeiro, ID ; Santos, AF ; Nery, F
Date: 2022
Persistent ID: https://hdl.handle.net/10216/151678
Origin: Repositório Aberto da Universidade do Porto
Subject(s): Dorfman-Chanarin syndrome; Inborn errors of metabolism; Liver transplantation; Metabolic associated fatty liver disease
Metabolic associated fatty liver disease became the most common form of chronic liver disease, in the vast majority of the cases related to increased insulin resistance or metabolic dysregulation. Yet, other causes may be implied. We report the late diagnosis of Dorfman-Chanarin syndrome in a non-alcoholic steatohepatitis previously labeled cirrhotic middle-aged man, with consanguineous parents, complicated with hepatocellular carcinoma. Congenital ichthyosis, neurosensory hearing loss and elevated muscular enzymes hit on the track of Dorfman-Chanarin syndrome. The genetic analysis uncovered a first-time described homozygotic nonsense mutation in the ABHD5 gene, responsible for coding the ABHD5 protein. The patient was successfully submitted to liver transplantation. Inborn errors of metabolism are a rare cause of metabolic associated fatty liver disease, but they need to be kept in consideration in all patients who present with atypical clinical features. This shall raise the awareness of physicians to rare forms of presentation since it may imply not only a different prognosis, but also other actions, like particular therapies as liver transplantation due to related complications of cirrhosis, or familial screening. © 2021 Sociedade Portuguesa de Gastrenterologia.
