From hypertransaminasemia to mucopolysaccharidosis IIIAReport as inadecuate




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Italian Journal of Pediatrics

, 40:97

Neurology, Behaviour and Development

Abstract

ᅟMucopolysaccharidosis type III MPS III; Sanfilippo syndrome is a metabolic disorder characterized by the deficiency of a lysosomal enzyme catalyzing the catabolic pathway of heparan sulphate. MPS III presents with progressive mental deterioration, speech delay and behavioural problems with subtle somatic features, which can often lead to misdiagnosis with idiopathic developmental-speech delay, attention deficit-hyperactivity disorder or autism. We report a case of a 5-year-old boy with developmental delay and behaviour problems admitted to the Department of Paediatrics due to chronic hypertransaminasemia. The patient developed normally until the age of 2 years when he was referred to a paediatric neurologist for suspected motor and speech delay. Liver function tests were unexpectedly found elevated at the age of 3.5 years. Physical examination revealed obesity, mildly coarse facial features and stocky hands. He showed mental retardation and mild motor delay. The clinical picture strongly suggested mucopolysaccharidosis. The diagnosis of MPS IIIA was confirmed by decreased activity of heparan N-sulfatase in leucocytes.

ConclusionWe strongly recommend screening for MPS III in children with severe behavioural abnormalities with hyperactivity, psychomotor or speech deterioration and failure to achieve early developmental milestones particularly with facial dysmorphism.

KeywordsMucopolysaccharidosis type IIIA Sanfilippo syndrome Hypertransaminasemia AbbreviationsADHDAttention deficit-hyperactivity disorder

ALTAlanine aminotransferase

ASTAspartate aminotransferase

CKCreatine kinase

CMVCytomegalovirus

EBVEbstein – Barr virus

GAGGlycosaminoglycan

GGTγ-glutamyltranspeptydase

HBVHepatitis B virus

HbsHepatitis B surface antigen

HCVHepatitis C virus

MPSMucopolysaccharidosis

NASHNon-alcoholic steatohepatitis

Electronic supplementary materialThe online version of this article doi:10.1186-s13052-014-0097-z contains supplementary material, which is available to authorized users.

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Author: Paulina Krawiec - Elżbieta Pac-Kożuchowska - Beata Mełges - Agnieszka Mroczkowska-Juchkiewicz - Stanisław Skomra - Agnies

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