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COVID-19: Implications for Children with Special Needs

Publication Type : Case Reports

Publisher : Elsevier

Source : Journal for ReAttach therapy and developmental diversities

Url : https://doi.org/10.1016/j.seizure.2019.07.011

Campus : Faridabad

School : School of Medicine

Year : 2019

Abstract : Glucose transporter-1 (GLUT1)/SLC2A1 is expressed at the highest levels in brain capillaries, astroglia, and erythrocytes. GLUT1-deficiency syndrome is a neurological disorder resulting primarily from aberrant glucose transport into the brain. Clinically, it is classified as GLUT1-deficiency syndrome with epilepsy and without epilepsy. The phenotypic spectrum of GLUT1- deficiency syndrome expanded over last two decades, encompassing a varying combination of epilepsies (absence, atypical absence, myoclonic, myoclonic-astatic, refractory generalized epilepsy, intractable infantile epilepsy etc.), movement disorders (paroxysmal exercise-induced dyskinesia, ataxia, etc.), and developmental delay. Pointers to diagnosis include a classical phenotype: early-onset absences, fasting-induced paroxysms (clinical and electroencephalographic), low cerebrospinal fluid (CSF) glucose (<50 mg/dl; CSF to blood glucose ratio<0.6) and lactate (<1.4 mmol/L), and a remarkable response to ketogenic diet (KD) [1]. Early diagnosis and treatment are rewarding. This report adds a novel presentation to the evolving phenotype of GLUT1-deficiency syndrome.

Cite this Research Publication : Gupta, Juhi, Priyanka Madaan, and Sheffali Gulati. "COVID-19: Implications for children with special needs." Journal for ReAttach therapy and developmental diversities 3, no. 1 (2020): 1-3.

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