ICNApedia - contentThe Child Neurology Wiki
https://icnapedia.org/wiki/
2024-03-29T13:44:21+00:00ICNApedia
https://icnapedia.org/wiki/
https://icnapedia.org/wiki/_media/favicon.icotext/html2024-03-28T14:11:46+00:00biju.hameed@gmail.com (biju.hameed@gmail.com@undisclosed.example.com)Self Injurious Behaviour (SIB)
https://icnapedia.org/wiki/content/self_injurious_behaviour?rev=1711635106&do=diff
Self Injurious Behaviour (SIB)
SIB refers to a class of behaviors which the individual inflicts upon his/herself that have the potential to result in physical injury, more specifically tissue damage. SIB may manifest in numerous ways, including but not limited to head banging, self-cutting, self-choking, self-biting, self-scratching, hair yanking, and hand mouthingtext/html2024-03-28T13:03:32+00:00biju.hameed@gmail.com (biju.hameed@gmail.com@undisclosed.example.com)Self Injury Trauma (SIT) Scale - created
https://icnapedia.org/wiki/content/self-injury_trauma_sit_scale?rev=1711631012&do=diff
Self Injury Trauma (SIT) Scale
The SIT scale aims to categorize and measure the harm caused by an act of Self Injurious Behaviour. Assessors note the location of the SIB, the number of occurrences, the severity of the wounds, and the type of injuries (such as redness, bruising, skin breakage/lacerations, fractures, contusions, etc). Once the locations of individual SIB injuries are evaluated, an overall score is calculated. This score takes into account the number of SIB topographies (rated on …text/html2024-03-24T21:09:24+00:00biju.hameed@gmail.com (biju.hameed@gmail.com@undisclosed.example.com)Pyridoxal 5 Phosphate Dependent Epilepsy
https://icnapedia.org/wiki/content/pyridoxal_5_-phosphate-dependent_epilepsy?rev=1711314564&do=diff
Pyridoxal 5 Phosphate Dependent Epilepsy
PNPO deficiency (OMIM 6032870) is an autosomal recessive inborn error of metabolism that leads to a seizure disorder, presenting in the newborn period (neonatal epileptic encephalopathy) or early infancy, that can be treated with pyridoxal 5’-phosphate but (classically) not pyridoxine. Seizures are often characterized by irregular involuntary muscle contractions (myoclonus), abnormal eye movements, and convulsions.text/html2024-03-23T20:59:39+00:00biju.hameed@gmail.com (biju.hameed@gmail.com@undisclosed.example.com)Index
https://icnapedia.org/wiki/content/index?rev=1711227579&do=diff
Index
* Absence Seizures
* Acetazolamide
* Acquired epileptiform aphasia
* Acylcarnitines
* Aicardi syndrome
* Aicardi-Goutières syndrome
* Albumin
* Alpha Amino Adipic Semialdehyde
* Alpha-1 antitrypsin, serum
* Alpha-Feto protein, serum
* Anakinra
* Atypical benign partial epilepsy
* Benign epilepsy with centrotemporal spikes
* Benign familial infantile epilepsy
* Benign familial neonatal epilepsy
* Benign neonatal sleep myoclonus
* Benign non-epileptic infantile spasms
* Be…text/html2024-03-23T20:47:24+00:00biju.hameed@gmail.com (biju.hameed@gmail.com@undisclosed.example.com)Developmental and/or Epileptic Encephalopathy with spike-wave activation in sleep (D/EE-SWAS) - [EEG]
https://icnapedia.org/wiki/content/developmental_and/or_epileptic_encephalopathy_with_spike-wave_activation_in_sleep_d/ee-swas?rev=1711226844&do=diff
Developmental and/or Epileptic Encephalopathy with spike-wave activation in sleep (D/EE-SWAS)
Developmental and/or Epileptic Encephalopathy with spike-wave activation in sleep (D/EE-SWAS),refers to a spectrum of conditions that are characterized by thetext/html2024-03-23T19:48:52+00:00biju.hameed@gmail.com (biju.hameed@gmail.com@undisclosed.example.com)Epileptic encephalopathy with continuous spike-waves during sleep
https://icnapedia.org/wiki/content/epileptic_encephalopathy_with_continuous_spike-waves_during_sleep?rev=1711223332&do=diff
Epileptic encephalopathy with continuous spike-waves during sleep
The term Developmental and/or Epileptic Encephalopathy with spike-wave activation in sleep (D/EE-SWAS)has been proposed which,refers to a spectrum of conditions that are characterized by the EEG feature of spike-wave activation in sleep, share similar clinical features and management implications. This syndrome now incorporates the syndromes previously named Landau-Kleffner syndrome, Epileptic Encephalopathy with Continuous Spike…text/html2024-03-23T19:44:30+00:00biju.hameed@gmail.com (biju.hameed@gmail.com@undisclosed.example.com)Self-Limited Epilepsy with Centrotemporal Spikes (SeLECTS) - [Treatment]
https://icnapedia.org/wiki/content/self_limited_epilepsy_with_centrotemporal_spikes_selects?rev=1711223070&do=diff
Self-Limited Epilepsy with Centrotemporal Spikes (SeLECTS)
(formerly called childhood epilepsy with centrotemporal spikes, benign epilepsy of childhood with centrotemporal spikes or Benign Rolandic Epilepsy)
* Self-Limited Epilepsy with Centrotemporal Spikes (SeLECTS), is the most common focal epilepsy syndrome of childhood, accounting for 15–20% of all childhood epilepsies.text/html2024-03-23T07:05:16+00:00biju.hameed@gmail.com (biju.hameed@gmail.com@undisclosed.example.com)Aicardi-Goutières syndrome - [Aicardi-Goutières syndrome]
https://icnapedia.org/wiki/content/aicardi-goutieres_syndrome?rev=1711177516&do=diff
Aicardi-Goutières syndrome
AGS is distinct from the similarly named Aicardi syndrome (characterized by absence of a brain structure (corpus callosum), and spinal, skeletal, and eye abnormalities
Aicardi-Goutieres syndrome (AGS) is a genetic encephalopathy characterized by the inappropriate induction of a type I interferon-mediated immune response and usually results in severe cognitive and physical morbidities. It is named aftertext/html2024-03-23T06:59:36+00:00biju.hameed@gmail.com (biju.hameed@gmail.com@undisclosed.example.com)Benign Rolandic Epilepsy
https://icnapedia.org/wiki/content/benign_rolandic_epilepsy?rev=1711177176&do=diff
Benign Rolandic Epilepsy
see Self-Limited Epilepsy with Centrotemporal Spikes (SeLECTS)text/html2024-03-22T22:32:32+00:00biju.hameed@gmail.com (biju.hameed@gmail.com@undisclosed.example.com)dee.png - created
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<img src="https://icnapedia.org/wiki/_media/content/dee.png?w=500&h=500&tok=c14f58" alt="dee.png" loading="lazy" width="500" height="500" />text/html2024-03-22T22:07:56+00:00biju.hameed@gmail.com (biju.hameed@gmail.com@undisclosed.example.com)Childhood Epilepsy with centrotemporal spikes
https://icnapedia.org/wiki/content/childhood_epilepsy_with_centrotemporal_spikes?rev=1711145276&do=diff
Childhood Epilepsy with centrotemporal spikes
see Self-Limited Epilepsy with Centrotemporal Spikes (SeLECTS)text/html2024-03-22T21:32:58+00:00biju.hameed@gmail.com (biju.hameed@gmail.com@undisclosed.example.com)Benign epilepsy with centrotemporal spikes - created
https://icnapedia.org/wiki/content/benign_epilepsy_with_centrotemporal_spikes?rev=1711143178&do=diff
Benign epilepsy with centrotemporal spikes
see Childhood Epilepsy with centrotemporal spikestext/html2024-03-22T21:25:41+00:00biju.hameed@gmail.com (biju.hameed@gmail.com@undisclosed.example.com)Methylphenidate Preparations - [Methylphenidate Preparations]
https://icnapedia.org/wiki/content/methylphenidate?rev=1711142741&do=diff
Methylphenidate Preparations
Methylphenidate (MPH) is available in 2 different isomer formulations. It is essential to know which formulation you are dealing with when converting from one stimulant to another. Those conversions are less precise if the new medication has a different formulation of isomers than the old one.text/html2024-03-19T18:21:23+00:00biju.hameed@gmail.com (biju.hameed@gmail.com@undisclosed.example.com)Spikes and Sharp Waves - [Polyspike-and-slow-wave complex]
https://icnapedia.org/wiki/content/spikes?rev=1710872483&do=diff
Spikes and Sharp Waves
Spikes, sharp waves, spike & waves are common EEG wave forms.
Spike wave
* A transient, clearly distinguished from background activity, with pointed peak at a conventional time scale and duration from 20 to less than 70 ms.text/html2024-03-19T18:19:35+00:00biju.hameed@gmail.com (biju.hameed@gmail.com@undisclosed.example.com)polyspike-and-waves.png - created
https://icnapedia.org/wiki/?image=content%3Apolyspike-and-waves.png&ns=content&rev=1710872375&tab_details=history&media_do=diff&do=media
<img src="https://icnapedia.org/wiki/_media/content/polyspike-and-waves.png?w=500&h=500&tok=71ec43" alt="polyspike-and-waves.png" loading="lazy" width="500" height="500" />text/html2024-03-19T18:07:55+00:00biju.hameed@gmail.com (biju.hameed@gmail.com@undisclosed.example.com)spike-and-wave.png - created
https://icnapedia.org/wiki/?image=content%3Aspike-and-wave.png&ns=content&rev=1710871675&tab_details=history&media_do=diff&do=media
<img src="https://icnapedia.org/wiki/_media/content/spike-and-wave.png?w=500&h=500&tok=eae071" alt="spike-and-wave.png" loading="lazy" width="500" height="500" />text/html2024-03-19T17:55:39+00:00biju.hameed@gmail.com (biju.hameed@gmail.com@undisclosed.example.com)sharp-and-spikes.png - created
https://icnapedia.org/wiki/?image=content%3Asharp-and-spikes.png&ns=content&rev=1710870939&tab_details=history&media_do=diff&do=media
<img src="https://icnapedia.org/wiki/_media/content/sharp-and-spikes.png?w=500&h=500&tok=90b659" alt="sharp-and-spikes.png" loading="lazy" width="500" height="500" />text/html2024-03-19T17:15:29+00:00biju.hameed@gmail.com (biju.hameed@gmail.com@undisclosed.example.com)bifrontalspikes-min.png - created
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<img src="https://icnapedia.org/wiki/_media/content/bifrontalspikes-min.png?w=500&h=500&tok=a04569" alt="bifrontalspikes-min.png" loading="lazy" width="500" height="500" />text/html2024-03-19T17:11:26+00:00biju.hameed@gmail.com (biju.hameed@gmail.com@undisclosed.example.com)bifrontalspikes.png - created
https://icnapedia.org/wiki/?image=content%3Aeeg%3Abifrontalspikes.png&ns=content%3Aeeg&rev=1710868286&tab_details=history&media_do=diff&do=media
<img src="https://icnapedia.org/wiki/_media/content/eeg/bifrontalspikes.png?w=500&h=500&tok=d672ad" alt="bifrontalspikes.png" loading="lazy" width="500" height="500" />text/html2024-03-19T17:06:15+00:00biju.hameed@gmail.com (biju.hameed@gmail.com@undisclosed.example.com)Childhood Absence Epilepsy - [Differentiating between CAE and JAE]
https://icnapedia.org/wiki/content/childhood_absence_epilepsy?rev=1710867975&do=diff
Childhood Absence Epilepsy
childhood_absence_epilepsy ccna1h
* Childhood absence epilepsy (CAE) is an age-dependent, idiopathic form of generalised epilepsy (IGE) characterised by multiple absence seizures per day, as well as bilateral, symmetrical, and synchronous discharges of 3-Hz generalised spike and waves (GSW) in the electroencephalogram.