Literature DB >> 22194384

Closed Meningo(encephalo)cele: a new feature in Hunter syndrome.

R Manara1, E Priante, M Grimaldi, L Santoro, G Polonara, R Parini, M Scarpa.   

Abstract

BACKGROUND AND
PURPOSE: Hunter syndrome (MPS type II) is a rare X-linked recessive disease caused by lysosomal enzyme iduronate-2-sulfatase deficiency, characterized by frequent and variable brain and skull involvement. Our objective was determine the frequency of closed cephaloceles in a large cohort of subjects affected with Hunter syndrome and to investigate possible correlations with clinical and neuroradiologic findings.
MATERIALS AND METHODS: Brain MR imaging of 33 patients (32 males and 1 female, age range 2.5-30.8 years, mean age 10.4 years) affected with Hunter syndrome were retrospectively evaluated. Eleven (age range 3.6-30.8 years; mean age 15.1) presented with an "attenuated" phenotype, while 22 (age range 2.5-19.1 years; mean age 8.2) had a "severe" phenotype.
RESULTS: A closed cephalocele was detected in 9/33 patients (27%) at the level of anterior and middle fossa in 6 and 3 cases, respectively; 6/9 subjects were affected with the attenuated phenotype and 1/9 suffered from epilepsy. Closed cephaloceles did not show a significant association with other brain and spine MR imaging features of Hunter disease, such as enlargement of perivascular spaces, cisterna magna, pituitary sella, ventricles and subarachnoid spaces, craniosynostosis, dens hypoplasia, white matter abnormalities, spinal stenosis due to periodontoid cap, platyspondylia, or intervertebral disk anomalies.
CONCLUSIONS: Closed cephaloceles are frequent in Hunter syndrome and should be considered a neuroradiologic feature of this disease.

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Mesh:

Year:  2011        PMID: 22194384      PMCID: PMC7968812          DOI: 10.3174/ajnr.A2867

Source DB:  PubMed          Journal:  AJNR Am J Neuroradiol        ISSN: 0195-6108            Impact factor:   3.825


  16 in total

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Journal:  Am J Otolaryngol       Date:  2006 Nov-Dec       Impact factor: 1.808

Review 2.  Spontaneous encephaloceles of the temporal lobe.

Authors:  Joshua J Wind; Anthony J Caputy; Fabio Roberti
Journal:  Neurosurg Focus       Date:  2008       Impact factor: 4.047

3.  Magnetic resonance imaging of the brain, neck and cervical spine in mild Hunter's syndrome (mucopolysaccharidoses type II).

Authors:  V J Parsons; D G Hughes; J E Wraith
Journal:  Clin Radiol       Date:  1996-10       Impact factor: 2.350

4.  Brain magnetic resonance imaging in 23 patients with mucopolysaccharidoses and the effect of bone marrow transplantation.

Authors:  T Seto; K Kono; K Morimoto; Y Inoue; H Shintaku; H Hattori; O Matsuoka; T Yamano; A Tanaka
Journal:  Ann Neurol       Date:  2001-07       Impact factor: 10.422

Review 5.  Multidisciplinary management of Hunter syndrome.

Authors:  Joseph Muenzer; M Beck; C M Eng; M L Escolar; R Giugliani; N H Guffon; P Harmatz; W Kamin; C Kampmann; S T Koseoglu; B Link; R A Martin; D W Molter; M V Muñoz Rojas; J W Ogilvie; R Parini; U Ramaswami; M Scarpa; I V Schwartz; R E Wood; E Wraith
Journal:  Pediatrics       Date:  2009-11-09       Impact factor: 7.124

6.  Brain MRI in mucopolysaccharidosis: effect of aging and correlation with biochemical findings.

Authors:  L Vedolin; I V D Schwartz; M Komlos; A Schuch; A C Azevedo; T Vieira; F K Maeda; A M Marques da Silva; R Giugliani
Journal:  Neurology       Date:  2007-08-28       Impact factor: 9.910

Review 7.  Neurological findings in Hunter disease: pathology and possible therapeutic effects reviewed.

Authors:  S Al Sawaf; E Mayatepek; B Hoffmann
Journal:  J Inherit Metab Dis       Date:  2008-07-13       Impact factor: 4.982

Review 8.  Management of meningoencephalic herniation of the temporal bone: Personal experience and literature review.

Authors:  Mario Sanna; Paolo Fois; Fois Paolo; Alessandra Russo; Maurizio Falcioni
Journal:  Laryngoscope       Date:  2009-08       Impact factor: 3.325

Review 9.  Recognition and diagnosis of mucopolysaccharidosis II (Hunter syndrome).

Authors:  Rick Martin; Michael Beck; Christine Eng; Roberto Giugliani; Paul Harmatz; Verónica Muñoz; Joseph Muenzer
Journal:  Pediatrics       Date:  2008-02       Impact factor: 7.124

Review 10.  Mucopolysaccharidosis type II (Hunter syndrome): a clinical review and recommendations for treatment in the era of enzyme replacement therapy.

Authors:  J Edmond Wraith; Maurizio Scarpa; Michael Beck; Olaf A Bodamer; Linda De Meirleir; Nathalie Guffon; Allan Meldgaard Lund; Gunilla Malm; Ans T Van der Ploeg; Jiri Zeman
Journal:  Eur J Pediatr       Date:  2007-11-23       Impact factor: 3.183

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  3 in total

Review 1.  Mucopolysaccharidoses: overview of neuroimaging manifestations.

Authors:  Manal Nicolas-Jilwan; Moeenaldeen AlSayed
Journal:  Pediatr Radiol       Date:  2018-05-11

2.  Chiari 1 malformation and holocord syringomyelia in hunter syndrome.

Authors:  Renzo Manara; Daniela Concolino; Angelica Rampazzo; Alessandra Zanetti; Rossella Tomanin; Roberto Faggin; Maurizio Scarpa
Journal:  JIMD Rep       Date:  2013-07-02

3.  Imaging findings of mucopolysaccharidoses: a pictorial review.

Authors:  Stefano Palmucci; Giancarlo Attinà; Maria Letizia Lanza; Giuseppe Belfiore; Giuseppina Cappello; Pietro Valerio Foti; Pietro Milone; Domenico Di Bella; Rita Barone; Agata Fiumara; Giovanni Sorge; Giovanni Carlo Ettorre
Journal:  Insights Imaging       Date:  2013-05-05
  3 in total

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