Literature DB >> 16970890

Proton magnetic resonance spectroscopy and diffusion-weighted imaging in isolated sulfite oxidase deficiency.

Florian Eichler1, Wen-Hann Tan, Vivian E Shih, P Ellen Grant, Kalpathy Krishnamoorthy.   

Abstract

Isolated sulfite oxidase deficiency is a rare autosomal recessive disorder of the newborn that can be mistaken for neonatal asphyxia. Diffusion-weighted imaging of the brain demonstrates widespread diffusion restriction, and proton magnetic resonance spectroscopy shows an elevated lactate level, a decrease in the ratio of N-acetylaspartate to creatine, and a rise in the ratio of choline to creatine. This precedes severe cystic encephalomalacia and suggests that the energy failure associated with neuronal dysfunction and myelin disintegration occurs early in isolated sulfite oxidase deficiency.

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Year:  2006        PMID: 16970890     DOI: 10.1177/08830738060210090601

Source DB:  PubMed          Journal:  J Child Neurol        ISSN: 0883-0738            Impact factor:   1.987


  7 in total

1.  Distinctive pattern of restricted diffusion in a neonate with molybdenum cofactor deficiency.

Authors:  Nicholas V Stence; Curtis R Coughlin; Laura Z Fenton; Janet A Thomas
Journal:  Pediatr Radiol       Date:  2012-12-19

2.  Delineating the phenotypic spectrum of sulfite oxidase and molybdenum cofactor deficiency.

Authors:  Albert L Misko; Ye Liang; Joshua B Kohl; Florian Eichler
Journal:  Neurol Genet       Date:  2020-07-14

Review 3.  Neonatal neuroimaging findings in inborn errors of metabolism.

Authors:  Andrea Poretti; Susan I Blaser; Maarten H Lequin; Ali Fatemi; Avner Meoded; Frances J Northington; Eugen Boltshauser; Thierry A G M Huisman
Journal:  J Magn Reson Imaging       Date:  2012-05-07       Impact factor: 4.813

Review 4.  MR spectroscopy in pediatric neuroradiology.

Authors:  Roberto Liserre; Lorenzo Pinelli; Roberto Gasparotti
Journal:  Transl Pediatr       Date:  2021-04

5.  ETHE1 and MOCS1 deficiencies: Disruption of mitochondrial bioenergetics, dynamics, redox homeostasis and endoplasmic reticulum-mitochondria crosstalk in patient fibroblasts.

Authors:  Mateus Grings; Bianca Seminotti; Anuradha Karunanidhi; Lina Ghaloul-Gonzalez; Al-Walid Mohsen; Peter Wipf; Johan Palmfeldt; Jerry Vockley; Guilhian Leipnitz
Journal:  Sci Rep       Date:  2019-09-02       Impact factor: 4.379

6.  Case Report: Electroencephalography in a neonate with isolated sulfite oxidase deficiency - a case report and literature review.

Authors:  Andreea M Pavel; Carol M Stephens; Sean R Mathieson; Brian H Walsh; Brian McNamara; Niamh McSweeney; Geraldine B Boylan
Journal:  HRB Open Res       Date:  2021-11-23

7.  Postmortem whole-genome sequencing on a dried blood spot identifies a novel homozygous SUOX variant causing isolated sulfite oxidase deficiency.

Authors:  Mallory J Owen; Jerica Lenberg; Annette Feigenbaum; Jeffrey Gold; Kevin Chau; Zaira Bezares-Orin; Yan Ding; Shimul Chowdhury; Stephen F Kingsmore
Journal:  Cold Spring Harb Mol Case Stud       Date:  2021-06-11
  7 in total

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