Literature DB >> 1563430

Computed tomography in maple syrup urine disease.

A Taccone1, M C Schiaffino, R Cerone, M P Fondelli, C Romano.   

Abstract

Maple Syrup Urine Disease (MSUD) is an inherited metabolic disorder characterized by a severe, usually lethal, neonatal course in the early stages with pseudotumor cerebri and pathologically documented increased cerebral water content. CT and MRI studies in MSUD are few and the data are overlapping. This study reports CT features before and after dietary treatment in three patients; two with classical MSUD and one with an intermediate variant of MSUD. At diagnosis, CT consistently showed evidence of abnormally high lucidity involving not only white matter, but also areas of grey matter, particularly the pallidum. Furthermore, these CT changes are present both in the acute phase of classical MSUD and in an intermediate variant of the disease. The observed abnormalities evolve favorably under dietary treatment, simultaneously with clinical and neurological improvement. It is concluded that the observed CT changes indicate a diagnosis of MSUD and are relevant findings in the neuroradiologic differential diagnosis in acutely ill newborns, in which a metabolic disease may be not immediately suspected.

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Year:  1992        PMID: 1563430     DOI: 10.1016/0720-048x(92)90089-r

Source DB:  PubMed          Journal:  Eur J Radiol        ISSN: 0720-048X            Impact factor:   3.528


  2 in total

1.  Imaging in classic form of maple syrup urine disease: a rare metabolic central nervous system.

Authors:  Aditi Jain; K Jagdeesh; Ranoji Mane; Saurabh Singla
Journal:  J Clin Neonatol       Date:  2013-04

2.  Imaging Findings in Maple Syrup Urine Disease: A Case Report.

Authors:  Anjaneya S Kathait; Paulo Puac; Mauricio Castillo
Journal:  J Pediatr Neurosci       Date:  2018 Jan-Mar
  2 in total

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