Literature DB >> 7477867

Neuroradiological findings in the carbohydrate-deficient glycoprotein syndrome.

S Akaboshi1, K Ohno, K Takeshita.   

Abstract

The carbohydrate-deficient glycoprotein syndrome is a newly recognised genetic disorder characterised by mental retardation, liver disfunction during infancy, cerebellar ataxia and atrophy, polyneuropathy, growth retardation, stroke-like episodes, and the appearance of carbohydrate-deficient fractions of multiple glycoproteins in the serum. The neuroradiological findings have been known as features of olivopontocerebellar atrophy. However, whether the abnormalities in the cerebellum and brain stem progress after birth is not known. We have carried out serial CT and MRI on three Japanese patients with this syndrome at different ages. A small cerebellum, with peculiar enlargement of the cisterna magna, and a small brain stem are present in infancy and atrophy of the anterior vermis and from before backwards in the cerebellar hemispheres seem to progress throughout early childhood.

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Year:  1995        PMID: 7477867     DOI: 10.1007/bf00600103

Source DB:  PubMed          Journal:  Neuroradiology        ISSN: 0028-3940            Impact factor:   2.804


  11 in total

1.  Posterior fossa malformations.

Authors:  N R Altman; T P Naidich; B H Braffman
Journal:  AJNR Am J Neuroradiol       Date:  1992 Mar-Apr       Impact factor: 3.825

2.  Primary structure and functional expression of the inositol 1,4,5-trisphosphate-binding protein P400.

Authors:  T Furuichi; S Yoshikawa; A Miyawaki; K Wada; N Maeda; K Mikoshiba
Journal:  Nature       Date:  1989-11-02       Impact factor: 49.962

Review 3.  The carbohydrate-deficient glycoprotein syndromes: pre-Golgi and Golgi disorders?

Authors:  J Jaeken; H Carchon; H Stibler
Journal:  Glycobiology       Date:  1993-10       Impact factor: 4.313

Review 4.  Carbohydrate-deficient glycoprotein syndromes: peculiar group of new disorders.

Authors:  B A Hagberg; G Blennow; B Kristiansson; H Stibler
Journal:  Pediatr Neurol       Date:  1993 Jul-Aug       Impact factor: 3.372

5.  Abnormal short-latency somatosensory evoked potentials in two patients with carbohydrate-deficient glycoprotein syndrome.

Authors:  M Itoh; K Ohno; Y Tomita; K Takeshita
Journal:  Acta Paediatr       Date:  1993 Jun-Jul       Impact factor: 2.299

6.  Olivopontocerebellar atrophy of neonatal onset and disialotransferrin developmental deficiency syndrome.

Authors:  S P Horslen; P T Clayton; B N Harding; N A Hall; G Keir; B Winchester
Journal:  Arch Dis Child       Date:  1991-09       Impact factor: 3.791

7.  Sugar chains of serum transferrin from patients with carbohydrate deficient glycoprotein syndrome. Evidence of asparagine-N-linked oligosaccharide transfer deficiency.

Authors:  K Yamashita; H Ideo; T Ohkura; K Fukushima; I Yuasa; K Ohno; K Takeshita
Journal:  J Biol Chem       Date:  1993-03-15       Impact factor: 5.157

8.  Sialic acid-deficient serum and cerebrospinal fluid transferrin in a newly recognized genetic syndrome.

Authors:  J Jaeken; H G van Eijk; C van der Heul; L Corbeel; R Eeckels; E Eggermont
Journal:  Clin Chim Acta       Date:  1984-12-29       Impact factor: 3.786

9.  Electrospray ionization-mass spectrometric analysis of serum transferrin isoforms in patients with carbohydrate-deficient glycoprotein syndrome.

Authors:  K Yamashita; T Ohkura; H Ideo; K Ohno; M Kanai
Journal:  J Biochem       Date:  1993-12       Impact factor: 3.387

10.  A unique pattern of coagulation abnormalities in carbohydrate-deficient glycoprotein syndrome.

Authors:  C Van Geet; J Jaeken
Journal:  Pediatr Res       Date:  1993-05       Impact factor: 3.756

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  6 in total

Review 1.  The role of glycoproteins in neural development function, and disease.

Authors:  K C Breen; C M Coughlan; F D Hayes
Journal:  Mol Neurobiol       Date:  1998-04       Impact factor: 5.590

2.  High residual activity of PMM2 in patients' fibroblasts: possible pitfall in the diagnosis of CDG-Ia (phosphomannomutase deficiency).

Authors:  S Grünewald; E Schollen; E Van Schaftingen; J Jaeken; G Matthijs
Journal:  Am J Hum Genet       Date:  2001-01-11       Impact factor: 11.025

3.  Olivopontocerebellar atrophy leading to recognition of carbohydrate-deficient glycoprotein syndrome type I.

Authors:  L Pavone; A Fiumara; R Barone; R Rizzo; P Buttitta; W B Dobyns; J Jaeken
Journal:  J Neurol       Date:  1996-10       Impact factor: 4.849

4.  Congenital nephrotic syndrome: a novel phenotype of type I carbohydrate-deficient glycoprotein syndrome.

Authors:  M S van der Knaap; R A Wevers; L Monnens; C Jakobs; J Jaeken; J A van Wijk
Journal:  J Inherit Metab Dis       Date:  1996       Impact factor: 4.982

5.  The normal phenotype of Pmm1-deficient mice suggests that Pmm1 is not essential for normal mouse development.

Authors:  K Cromphout; W Vleugels; L Heykants; E Schollen; L Keldermans; R Sciot; R D'Hooge; P P De Deyn; K von Figura; D Hartmann; C Körner; G Matthijs
Journal:  Mol Cell Biol       Date:  2006-08       Impact factor: 4.272

Review 6.  The congenital disorders of glycosylation: a multifaceted group of syndromes.

Authors:  Erik A Eklund; Hudson H Freeze
Journal:  NeuroRx       Date:  2006-04
  6 in total

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