Literature DB >> 7709780

Cervical cord compression and severe hydrocephalus in a child with Saudi variant of multiple sulfatase deficiency. Report of case.

K R al-Moutaery1, A R Choudhury, M O Hassanen.   

Abstract

We report a 2.5-year-old boy with Saudi variant of multiple sulfatase deficiency (MSD or Austin's disease). He presented with the features of cervical cord compression and a severe form of hydrocephalus. The former was due to a thickened posterior arch of the atlas and the latter from a narrow foramen magnum and meningeal thickening. Decompression of the cord was achieved by removal of the posterior margin of the foramen magnum and posterior arch of the atlas, and followed by a duroplasty. At a later date, ventricular decompression was achieved by insertion of a ventricular-peritoneal shunt. NMR did not demonstrate white matter changes in the brain. In this regard the reported case differs from the earlier description of the Saudi Variant of MSD.

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Year:  1994        PMID: 7709780     DOI: 10.1007/bf01401468

Source DB:  PubMed          Journal:  Acta Neurochir (Wien)        ISSN: 0001-6268            Impact factor:   2.216


  8 in total

1.  Multiple sulphatase deficiency presenting at birth.

Authors:  M Burch; A H Fensom; M Jackson; T Pitts-Tucker; P J Congdon
Journal:  Clin Genet       Date:  1986-11       Impact factor: 4.438

2.  Saudi variant of multiple sulfatase deficiency.

Authors:  A al Aqeel; P T Ozand; J Brismar; G G Gascon; G Brismar; M Nester; N Sakati
Journal:  J Child Neurol       Date:  1992-04       Impact factor: 1.987

3.  Studies in metachromatic leukodystrophy. XII. Multiple sulfatase deficiency.

Authors:  J H Austin
Journal:  Arch Neurol       Date:  1973-04

4.  Multiple sulfatase deficiency.

Authors:  B W Soong; A C Casamassima; J K Fink; G Constantopoulos; A L Horwitz
Journal:  Neurology       Date:  1988-08       Impact factor: 9.910

5.  Complementation studies with clinical and biochemical characterizations of a new variant of multiple sulphatase deficiency.

Authors:  A Tanaka; M Hirabayashi; M Ishii; S Yamaoka; M Kawamura; M Nishida; G Isshiki
Journal:  J Inherit Metab Dis       Date:  1987       Impact factor: 4.982

6.  Early manifestations of multiple sulfatase deficiency.

Authors:  R D Burk; D Valle; G H Thomas; C Miller; A Moser; H Moser; K N Rosenbaum
Journal:  J Pediatr       Date:  1984-04       Impact factor: 4.406

7.  Metachromatic form of diffuse cerebral sclerosis. V. The nature and significance of low sulfatase activity: a controlled study of brain, liver and kidney in four patients with metachromatic leukodystrophy (MLD).

Authors:  J Austin; D Armstrong; L Shearer
Journal:  Arch Neurol       Date:  1965-12

8.  Ocular features of multiple sulfatase deficiency and a new variant of metachromatic leukodystrophy.

Authors:  J B Bateman; M Philippart; S J Isenberg
Journal:  J Pediatr Ophthalmol Strabismus       Date:  1984 Jul-Aug       Impact factor: 1.402

  8 in total
  2 in total

1.  Early neurosurgical intervention in spondyloepiphyseal dysplasias.

Authors:  E Al-Shail; A Al-Odaib; P T Ozand
Journal:  Childs Nerv Syst       Date:  2005-08-20       Impact factor: 1.475

2.  Neuro-ichthyotic Syndromes: A Case Series.

Authors:  Faruk Incecık; Ozlem M Herguner; Mehmet N Ozbek; Serdal Gungor; Mustafa Yılmaz; Wiliam B Rizzo; Gülen G Mert
Journal:  J Pediatr Neurosci       Date:  2018 Jan-Mar
  2 in total

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