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Ohtahara syndrome

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Review Articles from PubMed

Review articles summarize what is currently known about a disease. They discuss research previously published by others. The terms "Ohtahara syndrome" returned 1 free, full-text review articles. First 1 results:
Early-onset epileptic encephalopathies: Ohtahara syndrome and early myoclonic encephalopathy.
Last Updated: Oct 09, 2012

Ohtahara syndrome and early myoclonic encephalopathy are the earliest presenting of the epileptic encephalopathies. They are typically distinguished from each other according to specific clinical and etiologic criteria. Nonetheless, considerable overlap exists between the two syndromes ...

Ohtahara syndrome with emphasis on recent genetic discovery.
Last Updated: May 21, 2012

Ohtahara syndrome or Early Infantile Epileptic Encephalopathy (EIEE) with Suppression-Burst, is the most severe and the earliest developing age-related epileptic encephalopathy. Clinically, the syndrome is characterized by early onset tonic spasms associated with a severe and continuous ...

Ohtahara syndrome: with special reference to its developmental aspects for differentiating from early myoclonic encephalopathy.
Last Updated: May 20, 2013

Ohtahara syndrome (OS) is well known as a peculiar early onset epileptic syndrome with serious prognosis. The outline of OS, mainly in relation to the evolution with age, and differentiation from related conditions, particularly early myoclonic encephalopathy (EME) were mentioned.

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1 Free Review Articles 5 Review Articles

Editorials from PubMed

Editorial articles describe the outcome of a single study. They are the published results of original research. The terms "Ohtahara syndrome" returned 0 free, full-text editorial articles. First 0 results:
No publications were found for this category.
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Research Articles from PubMed

Research articles describe the outcome of a single study. They are the published results of original research. The terms "Ohtahara syndrome" returned 18 free, full-text research articles. First few results:
Biallelic DMXL2 mutations impair autophagy and cause Ohtahara syndrome with progressive course.
Last Updated: May 21, 2020

Ohtahara syndrome, early infantile epileptic encephalopathy with a suppression burst EEG pattern, is an aetiologically heterogeneous condition starting in the first weeks or months of life with intractable seizures and profound developmental disability. Using whole exome sequencing, ...

mutation in an infant with Ohtahara syndrome and neuroimaging findings: expanding the phenotype of neuronal migration disorders.
Last Updated: Feb 25, 2020

Neuronal migration disorders (NMDs) are a heterogeneous group of conditions caused by the abnormal migration of neuroblasts in the developing brain and nervous system, resulting in severe developmental impairment, intractable epilepsy and intellectual disability (Spalice 2009). To ...

Ictal PET in Ohtahara Syndrome With Hemimegalencephaly.
Last Updated: Apr 01, 2019

Ohtahara syndrome is one of the causes of infantile epilepsies, which presents with refractory seizures and characteristic EEG changes. It is often associated with structural anomalies in the brain. We report a case of 5-month-old girl with Ohtahara syndrome with hemimegalencephaly ...

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18 Free Research Articles 47 Research Articles