Literature DB >> 6262936

Intracranial calcification in oculodento-osseous dysplasia.

A Barnard, H Hamersma, J C de Villiers, P Beighton.   

Abstract

Oculodento-osseous dysplasia (ODOD) is a rare genetic disorder characterized by microphthalmia, hypoplasia of the dental enamel, dysplastic and sclerotic changes in the skeleton and various digital malformations. The occurrence of basal ganglion calcification in this condition is of considerable interest, particularly as it has some biochemical features in common with hypoparathyroidism and pseudohypoparathyroidism. The 2 patients presented in this article did not show any features of an extrapyramidal disorder, but both experienced progressive spasticity in the limbs. The neurological disturbance was not due to compression of the neuraxis by bony overgrowth, but to an associated neurological lesion of undetermined nature. The biochemical abnormalities are discussed but as yet no explanation for the association between intracranial calcification and ODOD can be offered.

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Mesh:

Year:  1981        PMID: 6262936

Source DB:  PubMed          Journal:  S Afr Med J


  3 in total

1.  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 2.  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

Review 3.  [Visualization of symmetric striopallidodentate calcinosis by using high-resolution susceptibility-weighted MR imaging. An account of the impact of different diagnostic methods of M. Fahr].

Authors:  J Böttcher; D Sauner; A Jentsch; H-J Mentzel; H Becker; J R Reichenbach; W A Kaiser
Journal:  Nervenarzt       Date:  2004-04       Impact factor: 1.214

  3 in total

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