Literature DB >> 8183459

MRI in cerebellar hypoplasia.

N deSouza1, R Chaudhuri, J Bingham, T Cox.   

Abstract

Cerebellar hypoplasia may present with a wide variety of neurological and systemic features, ranging from aplasia causing neonatal death to mild hypoplasia in an asymptomatic adult. MRI clearly documents the size of the cerebellum and any associated abnormalities. We describe 7 cases of cerebellar hypoplasia of varying aetiology--3 inherited, 2 associated with spinal dysraphism, 1 with Joubert's syndrome and 1 with pontine agenesis, probably as a result of basilar artery infarction in utero. T1- and T2-weighted images were obtained in each case and gadolinium-DTPA was administered in one. Associated features such as a Chiari malformation (2 cases), brain stem hypoplasia (2 cases), Dandy-Walker cyst and pachygyria (3 cases) and spinal dysraphism (2 cases) were clearly identified. Accurate documentation of these appearances assists in genetic counselling.

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Year:  1994        PMID: 8183459     DOI: 10.1007/bf00588085

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


  20 in total

1.  Cerebellar hypoplasia associated with systemic degeneration in early life.

Authors:  R M NORMAN; H URICH
Journal:  J Neurol Neurosurg Psychiatry       Date:  1958-08       Impact factor: 10.154

2.  An association of subtotal cerebellar agenesis with organoid nevus--a possible new variety of neurocutaneous syndrome.

Authors:  P J Wang; Y Maeda; T Izumi; K Yajima; M Hara; N Kobayashi; Y Fukuyama
Journal:  Brain Dev       Date:  1983       Impact factor: 1.961

3.  Cerebellar hypoplasia, communicating hydrocephalus and mental retardation in two brothers and a maternal uncle.

Authors:  W O Renier; F J Gabreëls; T W Hustinx; H O Thijssen; B G Ter Haar; E W Kroll; H Beckers
Journal:  Brain Dev       Date:  1983       Impact factor: 1.961

4.  Amyotrophic cerebellar hypoplasia: a specific form of infantile spinal atrophy.

Authors:  G A de León; W D Grover; C A D'Cruz
Journal:  Acta Neuropathol       Date:  1984       Impact factor: 17.088

5.  Joubert syndrome: a clinico-radiological study.

Authors:  B Kendall; D Kingsley; S R Lambert; D Taylor; P Finn
Journal:  Neuroradiology       Date:  1990       Impact factor: 2.804

6.  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

7.  Magnetic resonance imaging of infratentorial congenital brain malformations.

Authors:  S E Byrd
Journal:  J Natl Med Assoc       Date:  1989-09       Impact factor: 1.798

8.  Autosomal recessive congenital cerebellar hypoplasia.

Authors:  A Wichman; L M Frank; T E Kelly
Journal:  Clin Genet       Date:  1985-04       Impact factor: 4.438

9.  Autosomal recessive cerebellar hypoplasia.

Authors:  K D Mathews; A K Afifi; J W Hanson
Journal:  J Child Neurol       Date:  1989-07       Impact factor: 1.987

10.  Facial hemangioma with cerebrovascular anomalies and cerebellar hypoplasia.

Authors:  Y Mizuno; T Kurokawa; Y Numaguchi; N Goya
Journal:  Brain Dev       Date:  1982       Impact factor: 1.961

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  3 in total

1.  Disruption of cerebellar development: potential complication of extreme prematurity.

Authors:  Agnes Messerschmidt; Peter C Brugger; Eugen Boltshauser; Gerlinde Zoder; Walter Sterniste; Robert Birnbacher; Daniela Prayer
Journal:  AJNR Am J Neuroradiol       Date:  2005-08       Impact factor: 3.825

2.  Unilateral cerebellar hypoplasia with different clinical features.

Authors:  Gulcin Benbir; Simay Kara; Beyza Citci Yalcinkaya; Geysu Karhkaya; Beyhan Tuysuz; Naci Kocer; Cengiz Yalcinkaya
Journal:  Cerebellum       Date:  2011-03       Impact factor: 3.847

Review 3.  MRI of the fetal posterior fossa.

Authors:  Catherine Adamsbaum; Marie Laure Moutard; Christine André; Valérie Merzoug; Solène Ferey; Marie Pierre Quéré; Fanny Lewin; Catherine Fallet-Bianco
Journal:  Pediatr Radiol       Date:  2004-11-23
  3 in total

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