Literature DB >> 32643685

Van der Knaap Disease (Vanishing White Matter) - Unusual Presentation in a Neonate: A Case Report.

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


  1 in total

1.  Siblings with megalencephalic leukoencephalopathy with subcortical cysts van der Knaap disease.

Authors:  Saanida M P; Lin Varghese; Rinu Susan Thomas; Sandeep Govindan Prasad
Journal:  BJR Case Rep       Date:  2021-06-19
  1 in total

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