Screening for Variants in Egyptian Patients with Pontocerebellar Malformations.

INTRODUCTION

Pontocerebellar hypoplasia (PCH) represents a group of rare disorders with prenatal onset and time-dependent loss of brain parenchyma, predominantly affecting the cerebellum and pons with variable involvement of supratentorial structures. Radiologically and pathologically, they are characterized by small cerebellum and pons. Our study aimed to screen for the gene variants in Egyptian patients with PCH for proper counseling and to describe the brain MRI and the clinical phenotype and compare, them to those described in the literature.

METHODS

Thirty patients from thirty Egyptian families with a diagnosis of PCH based on neuroimaging findings were selected. Clinical evaluation, radiological findings, and genetic investigations were done for all patients.

RESULTS

The common missense variant c.919G>T (p.A307S) was identified in only 6 patients from six unrelated families (6/30; 20%) who showed different degrees of pontocerebellar malformations on brain imaging.

CONCLUSION

The presence of a dragonfly/butterfly-like pattern in the coronal section of the cerebellum recommends genetic testing of as a first step. For negative cases, whole-exome sequencing is essential to reach a definite diagnosis and determine the etiology.