Literature DB >> 8773286

Oculodental digital dysplasia: neuroimaging in a kindred.

L E Ginsberg1, T Jewett, R Grub, W T McLean.   

Abstract

Oculodental digital dysplasia (ODDD) is an uncommon inherited disorder with characteristic facial abnormalities, defects in dentition and syndactyly; previous reports have described neurologic dysfunction. We present neuroimaging features of a mother and daughter with ODDD; despite only the mother having neurologic dysfunction, the MRI findings in both are strikingly similar.

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Year:  1996        PMID： 8773286     DOI： 10.1007/bf00593230

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


  13 in total

1.  Oculodentodigital dysplasia.

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Journal:  J Pediatr       Date:  1963-07       Impact factor: 4.406

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4.  Three new cases of oculodentodigital (ODD) syndrome: development of the facial phenotype.

Authors:  M A Patton; K M Laurence
Journal:  J Med Genet       Date:  1985-10       Impact factor: 6.318

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Authors:  A G Farman; S N Smith; C J Nortjé
Journal:  Br Dent J       Date:  1977-06-21       Impact factor: 1.626

6.  Oculodentodigital dysplasia. Four new reports and a literature review.

Authors:  G F Judisch; A Martin-Casals; J W Hanson; W H Olin
Journal:  Arch Ophthalmol       Date:  1979-05

7.  Oculodento-osseous dysplasia: heterogeneity or variable expression?

Authors:  P Beighton; H Hamersma; M Raad
Journal:  Clin Genet       Date:  1979-09       Impact factor: 4.438

8.  Oculodentodigital dysplasia syndrome associated with abnormal cerebral white matter.

Authors:  D H Gutmann; E H Zackai; D M McDonald-McGinn; K H Fischbeck; J Kamholz
Journal:  Am J Med Genet       Date:  1991-10-01

9.  A family with oculodentodigital dysplasia.

Authors:  D M Weintraub; J L Baum; H M Pashayan
Journal:  Cleft Palate J       Date:  1975-07

10.  Intracranial calcification in oculodento-osseous dysplasia.

Authors:  A Barnard; H Hamersma; J C de Villiers; P Beighton
Journal:  S Afr Med J       Date:  1981-05-16
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  3 in total

Review 1.  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

2.  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

3.  Epilepsy as a rare neurologic manifestation of oculodentodigitalis dysplasia.

Authors:  Mohammad Barzegar; Mohammad Sayadnasiri; Aidin Tabrizi
Journal:  Iran J Child Neurol       Date:  2012
  3 in total

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