Distinctive Features of Hepatic Steatosis in Children: Is It Primary or Secondary to Inborn Errors of Metabolism?
Asuman Nur KarhanHayriye Hizarcioglu-GulsenErsin GumusZuhal AkçörenHülya DemirInci Nur Saltik TemizelDiclehan OrhanHasan ÖzenPublished in: Pediatric gastroenterology, hepatology & nutrition (2021)
Parents with consanguinity and positive family history, together with clinical and biochemical findings, may provide a high index of suspicion for IEM to distinguish primary steatosis from the consequence of a more complex disorder.