| Literature DB >> 32643685 |
Malay Jhancy1, Ammar Al Homsi2, Fatema Chowdhury2, Samiha Hossain2, Reshme Ahamed2.
Abstract
Van der Knaap disease, also known as megalencephalic leukoencephalopathy with subcortical cysts (MLC), is a rare autosomal disorder, with no exact prevalence but more than 150 cases were reported in the literature. It was more prevalent in some ethnicities where consanguinity is common.[1] It is usually characterized by infantile-onset macrocephaly, cerebral leukoencephalopathy and mild neurological symptoms, and a slow course of functional deterioration.[2] Diagnosis is determined by suggestive clinical features and MRI findings that include leukodystrophy and subcortical cysts. Herein, we present a rare occurrence of Van der Knaap disease, in a 24-day-old female neonate with similar MRI findings, who presented with neonatal seizures for evaluation.Entities:
Keywords: Megalencephaly leukoencephalopathy; Van der Knaap disease; seizures; subcortical cysts
Mesh:
Year: 2020 PMID: 32643685 DOI: 10.4103/0028-3886.289018
Source DB: PubMed Journal: Neurol India ISSN: 0028-3886 Impact factor: 2.117