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Table 1 Showing comparative literature review

From: A rare case report of non-syndromic unilateral cerebellar dysplasia and hypoplasia: a diagnostic enigma

Authors

Year of study

Methods

Findings

Conclusion

Soto-Ares et al. [1]

2000

In this study, there was a retrospective review of 46 MR examinations of patients presenting with developmental delay, hypotonia, and facial deformities to identify abnormal folia or fissures or both within cerebellar hemispheres or vermis suggesting cortical dysplasia

This study diagnosed cerebellar dysplasia in 17 patients, but it was isolated in only two patients

This study could conclude that cerebellar cortical dysplasias are common in cases with more widespread cerebral malformations

Baek [3]

2013

Case report

This report describes a case of isolated unilateral cerebellar cortical dysplasia with partial agenesis of corpus callosum. Foliation of contralateral cerebellar hemisphere and other structures in the posterior fossa were normal

It was suggested by the author that awareness of cerebellar cortical dysplasia and its embryologic background can be helpful for recognition of this mild form of cerebellar abnormality on high-quality MR imaging in clinical practices

Patel and Barkovich [6]

2002

MR images obtained in 70 patients with cerebellar malformations were retrospectively reviewed

In this study, non-syndromic (isolated) focal cerebellar dysplasia was seen in only two patients, while isolated cerebellar hypoplasia was diagnosed in six patients

This study proposed a scheme to organize cerebellar malformations

Chatur et al. [8]

2019

Case report

This is a case report of isolated cerebellar dysplasia in which, MRI brain revealed hemihypertrophy of left cerebellar hemisphere with disorganized architecture, fissural malorientation with individual folia running vertically rather than horizontally with disorganized foliation, abnormal arborization of white matter. Right cerebellar hemisphere and cerebellar vermis were normal. Cerebral parenchyma and Corpus callosum were normal

It was deduced by the authors that understanding of the basics of cerebellar embryology, knowledge of the imaging features, and clinical presentation aids in the precise diagnosis of this disorder and its optimal management

Babal and Aggarwal [This case report]

2023

Case report

Isolated cerebellar dysplasias with no other structural or signal abnormality in the rest of the brain

Notable isolated unilateral cerebellar dysplasia is a rare entity requiring symptomatic treatment and anomalous developmental process being the likely aetiology