Literature DB >> 6336193

Computed tomography in congenital ocular motor apraxia.

I Eda, S Takashima, T Kitahara, K Ohno, K Takeshita.   

Abstract

Unusual computed tomographic findings were observed in four patients with congenital ocular motor apraxia (COMA). These (CT) findings were characteristic in the posterior cranial fossa, with a dilated or deformed shape and size of the fourth ventricle, particularly its upper portion. One case revealed partial agenesis of the cerebellar vermis. It was suggested that the four patients subjected to CT showed abnormal topography of the cerebellar vermis or the brain stem. We postulate that these CT findings in COMA may have an important role in its pathogenesis.

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Year:  1984        PMID: 6336193     DOI: 10.1007/bf00327487

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


  14 in total

1.  Congenital ocular motor apraxia. Report of a case with a review of the literature.

Authors:  D A RIOPEL
Journal:  Am J Ophthalmol       Date:  1963-03       Impact factor: 5.258

2.  Congenital ocular motor apraxia in females.

Authors:  W L CAMPBELL; R ZELLER
Journal:  Arch Ophthalmol       Date:  1961-11

3.  A type of congenital ocular motor apraxia presenting jerky head movements.

Authors:  D G COGAN
Journal:  Trans Am Acad Ophthalmol Otolaryngol       Date:  1952 Nov-Dec

4.  Cerebral Integration of Ocular Movements.

Authors:  G Holmes
Journal:  Br Med J       Date:  1938-07-16

5.  A discussion of ocular motor apraxia with a case presentation.

Authors:  D J LYLE
Journal:  Trans Am Ophthalmol Soc       Date:  1961

6.  Cogan's congenital ocular motor apraxia in two successive generations.

Authors:  F Vassella; J Lütschg; M Mumenthaler
Journal:  Dev Med Child Neurol       Date:  1972-12       Impact factor: 5.449

7.  Congenital ocular motor apraxia: paediatric aspects.

Authors:  J Rendle-Short; B Appleton; J Pearn
Journal:  Aust Paediatr J       Date:  1973-10

8.  Familial agenesis of the cerebellar vermis. A syndrome of episodic hyperpnea, abnormal eye movements, ataxia, and retardation.

Authors:  M Joubert; J J Eisenring; J P Robb; F Andermann
Journal:  Neurology       Date:  1969-09       Impact factor: 9.910

9.  Joubert syndrome: episodic hyperpnea, abnormal eye movements, retardation and ataxia, associated with dysplasia of the cerebellar vermis.

Authors:  E Boltshauser; W Isler
Journal:  Neuropadiatrie       Date:  1977-02

10.  Joubert syndrome: a case confirmed by computerized tomography.

Authors:  P Curatolo; S Mercuri; E Cotroneo
Journal:  Dev Med Child Neurol       Date:  1980-06       Impact factor: 5.449

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  1 in total

1.  Intermittent horizontal saccade failure ('ocular motor apraxia') in children.

Authors:  C M Harris; F Shawkat; I Russell-Eggitt; J Wilson; D Taylor
Journal:  Br J Ophthalmol       Date:  1996-02       Impact factor: 4.638

  1 in total

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