Lead encephalopathy in an infant mimicking a neurometabolic disorder.

Versión para impresiónSend by emailVersión en PDF
TítuloLead encephalopathy in an infant mimicking a neurometabolic disorder.
Publication TypeJournal Article
Año de publicación2010
AutoresSahu, Jitendra K., Sharma Suvasini, Kamate Mahesh, Kumar Atin, Gulati Sheffali, Kabra Madhulika, and Kalra Veena
JournalJournal of child neurology
Volume25
Issue3
Pagination390-2
Date Published2010 Mar
Publication Languageeng
Abstract

We report the case of a 7-month-old child who presented with regression of milestones, seizures, altered sensorium, and vomiting. An elder sibling had died of similar complaints. Lead encephalopathy was considered because of presence of microcytic hypochromic anemia and dense metaphyseal bands on wrist radiogram. Magnetic resonance imaging (MRI) of the brain revealed diffuse dysmyelination involving both periventricular and subcortical white matter. Such diffuse changes have not been described previously. The child's father was operating an illicit lead-acid battery manufacturing unit at home. The child was subjected to chelation therapy, which was accompanied by environmental exposure source modification. He showed significant improvement. Our case highlights the importance of taking a detailed occupational history and considering lead poisoning in the differential diagnosis of encephalopathy of unidentifiable cause.

Alternate JournalJ. Child Neurol.