Hepatic Presentation of Late-Onset Multiple Acyl-CoA Dehydrogenase Deficiency (MADD): Case Report and Systematic Review
Diagnosis of pediatric steatohepatitis is a challenging issue due to a vast number of established and novel causes. Here, we report a child with Multiple Acyl-CoA Dehydrogenase Deficiency (MADD) presenting with an underrated muscle weakness, exercise intolerance and an atypically severe steatotic li...
Main Authors: | Maria Anna Siano, Claudia Mandato, Lucia Nazzaro, Gennaro Iannicelli, Gian Paolo Ciccarelli, Ferdinando Barretta, Cristina Mazzaccara, Margherita Ruoppolo, Giulia Frisso, Carlo Baldi, Salvatore Tartaglione, Francesco Di Salle, Daniela Melis, Pietro Vajro |
---|---|
Format: | Article |
Language: | English |
Published: |
Frontiers Media S.A.
2021-05-01
|
Series: | Frontiers in Pediatrics |
Subjects: | |
Online Access: | https://www.frontiersin.org/articles/10.3389/fped.2021.672004/full |
Similar Items
-
Fatty liver disease and hypertransaminasemia hiding the association of clinically silent Duchenne muscular dystrophy and hereditary fructose intolerance
by: Paolella Giulia, et al.
Published: (2012-10-01) -
Atypically Protracted Course of Liver Involvement in Kawasaki Disease. Case Report and Literature Review
by: Pamela Paglia, et al.
Published: (2021-07-01) -
Sudden cardiac death in young athletes: Literature review of molecular basis
by: Cristina Mazzaccara, et al.
Published: (2020-04-01) -
Uyuşturucu madde suçlarında bazı sosyal faktörler
by: Tülin Günşen İçli
Published: (1985-12-01) -
Madde Etkisi Şüphesi Altındaki Sürücülerde Tükürük Analizi
by: Serap Annette Akgür, et al.
Published: (2006-04-01)