Early myoclonic encephalopathy: Difference between revisions
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{{ | __NOTOC__ | ||
{{Infobox_Disease | | |||
Name = {{PAGENAME}} | | |||
Image = | | |||
Caption = | |||
DiseasesDB = | | |||
ICD10 = G 40.3| | |||
ICD9 = | | |||
MeshID = D004831| | |||
}} | |||
'''For patient information, click [[Insert page name here (patient information)|Insert page name here]]''' | |||
{{CMG}} ; | |||
{{SK}} neonatal myoclonic encephalopathy | |||
==Overview== | |||
Early myoclonic encephalopathy, is a seizure disorder that begins in the neonatal period. It has features like partial or fragmentary erratic myoclonic seizures,massive myoclonus, partial motor seizures (jerking movements of one side)and tonic seizures. | Early myoclonic encephalopathy, is a seizure disorder that begins in the neonatal period. It has features like partial or fragmentary erratic myoclonic seizures,massive myoclonus, partial motor seizures (jerking movements of one side)and tonic seizures. | ||
==Historical Perspective== | |||
==Classification== | |||
==Pathophysiology== | |||
=== Genetics === | |||
===Associated Conditions=== | |||
==Causes== | |||
==Differentiating type page name here from other Diseases== | |||
== Epidemiology and Demographics == | |||
== Risk Factors == | |||
== Screening == | |||
== Natural History, Complications, and Prognosis== | |||
== Diagnosis == | |||
=== Symptoms === | |||
===Family History=== | |||
=== Physical Examination === | |||
==== Appearance of the Patient ==== | |||
====Vital Signs==== | |||
====Skin==== | |||
====Head==== | |||
==== Eyes ==== | |||
==== Ear ==== | |||
====Nose==== | |||
====Throat ==== | |||
==== Heart ==== | |||
==== Lungs ==== | |||
==== Abdomen ==== | |||
==== Extremities ==== | |||
==== Neurologic ==== | |||
==== Other ==== | |||
=== Laboratory Findings === | |||
==== Biomarker Studies ==== | |||
====CT ==== | |||
==== MRI ==== | |||
==== Ultrasound ==== | |||
== Treatment == | |||
=== Pharmacotherapy === | |||
==== Acute Pharmacotherapies ==== | |||
==== Chronic Pharmacotherapies ==== | |||
=== Surgery and Device Based Therapy === | |||
==== Indications for Surgery ==== | |||
==== Pre-Operative Assessment ==== | |||
==== Post-Operative Management ==== | |||
===Primary Prevention=== | |||
====Genetic Counseling==== | |||
==References== | ==References== | ||
{{reflist|2}} | {{reflist|2}} | ||
{{ | {{WikiDoc Help Menu}} | ||
{{ | {{WikiDoc Sources}} | ||
[[Category:Disease]] | [[Category:Disease]] | ||
Revision as of 16:01, 9 August 2012
| Early myoclonic encephalopathy | |
| DiseasesDB = | |
| ICD-10 | G 40.3 |
|---|---|
| MeSH | D004831 |
For patient information, click Insert page name here Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] ;
Synonyms and keywords: neonatal myoclonic encephalopathy
Overview
Early myoclonic encephalopathy, is a seizure disorder that begins in the neonatal period. It has features like partial or fragmentary erratic myoclonic seizures,massive myoclonus, partial motor seizures (jerking movements of one side)and tonic seizures.