Literature DB >> 1659191

Oculodentodigital dysplasia syndrome associated with abnormal cerebral white matter.

D H Gutmann1, E H Zackai, D M McDonald-McGinn, K H Fischbeck, J Kamholz.   

Abstract

Oculodentodigital dysplasia (ODDD) syndrome is an uncommon inherited disorder with eye and facial abnormalities, syndactyly, and defects in tooth enamel. Some of the previously reported patients with ODDD syndrome also manifested spastic quadriparesis. We describe a patient with sporadic ODDD syndrome referred for evaluation of progressive spastic paraparesis. Magnetic resonance imaging of the brain demonstrated abnormal white matter, which suggests an explanation for the observed spastic paraparesis.

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Year:  1991        PMID: 1659191     DOI: 10.1002/ajmg.1320410106

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  16 in total

1.  A dominant connexin43 mutant does not have dominant effects on gap junction coupling in astrocytes.

Authors:  Sameh Wasseff; Charles K Abrams; Steven S Scherer
Journal:  Neuron Glia Biol       Date:  2011-03-04

2.  Oculodental digital dysplasia: neuroimaging in a kindred.

Authors:  L E Ginsberg; T Jewett; R Grub; W T McLean
Journal:  Neuroradiology       Date:  1996-01       Impact factor: 2.804

Review 3.  Gap junctions in inherited human disorders of the central nervous system.

Authors:  Charles K Abrams; Steven S Scherer
Journal:  Biochim Biophys Acta       Date:  2011-08-16

4.  Hot cross bun sign and prominent cerebellar peduncle involvement in a patient with oculodentodigital dysplasia.

Authors:  Vasilios C Constantinides; George P Paraskevas; Stefania Kalogera; Christos Yapijakis; Elisabeth Kapaki
Journal:  Neurol Sci       Date:  2020-07-16       Impact factor: 3.307

5.  GJA1 Variants Cause Spastic Paraplegia Associated with Cerebral Hypomyelination.

Authors:  L Saint-Val; T Courtin; P Charles; C Verny; M Catala; R Schiffmann; O Boespflug-Tanguy; F Mochel
Journal:  AJNR Am J Neuroradiol       Date:  2019-04-25       Impact factor: 3.825

6.  Oculodentodigital Dysplasia: A Hypomyelinating Leukodystrophy with a Characteristic MRI Pattern of Brain Stem Involvement.

Authors:  I Harting; S Karch; U Moog; A Seitz; P J W Pouwels; N I Wolf
Journal:  AJNR Am J Neuroradiol       Date:  2019-05-02       Impact factor: 3.825

7.  Magnetic resonance imaging pattern recognition in hypomyelinating disorders.

Authors:  Marjan E Steenweg; Adeline Vanderver; Susan Blaser; Alberto Bizzi; Tom J de Koning; Grazia M S Mancini; Wessel N van Wieringen; Frederik Barkhof; Nicole I Wolf; Marjo S van der Knaap
Journal:  Brain       Date:  2010-10       Impact factor: 13.501

Review 8.  Variable expression of neurological phenotype in autosomal recessive oculodentodigital dysplasia of two sibs and review of the literature.

Authors:  Shelagh K Joss; Sam Ghazawy; Susan Tomkins; Mushtaq Ahmed; John Bradbury; Eamonn Sheridan
Journal:  Eur J Pediatr       Date:  2007-05-03       Impact factor: 3.183

9.  The potency of the fs260 connexin43 mutant to impair keratinocyte differentiation is distinct from other disease-linked connexin43 mutants.

Authors:  Jared M Churko; Stephanie Langlois; Xinyue Pan; Qing Shao; Dale W Laird
Journal:  Biochem J       Date:  2010-08-01       Impact factor: 3.857

10.  Gap Junctions and Biophysical Regulation of Bone Cells.

Authors:  Shane A J Lloyd; Henry J Donahue
Journal:  Clin Rev Bone Miner Metab       Date:  2010-12-01
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