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العنوان
Pediatric Autoimmune Neuropsychiatric
Disorders Associated with Streptococcal
infection (PANDAS) – Review
المؤلف
Ahmed,Abdel-Moneam Said
هيئة الاعداد
باحث / Ahmed Abdel-Moneam Said
مشرف / Safeya Mahmoud Effat
مشرف / Mohamed Fekry Essa
مشرف / Soheir Helmy El-Ghonemy
الموضوع
Echocardiographic Findings in the<br>PANDAS subgroup-
تاريخ النشر
2012
عدد الصفحات
108.p:
اللغة
الإنجليزية
الدرجة
ماجستير
التخصص
الطب النفسي والصحة العقلية
تاريخ الإجازة
1/1/2012
مكان الإجازة
جامعة عين شمس - كلية الطب - Neuropsychiatry
الفهرس
Only 14 pages are availabe for public view

from 108

from 108

Abstract

Streptococcal infection in children is usually benign and selflimited,
however, in a small percentage of children, prominent neurologic
and/or psychiatric sequelae can occur. PANDAS (Pediatric Autoimmune
Neuropsychiatric Disorders Associated with Streptococcal infection) is a
well-defined syndrome in which tics (motor and/or vocal) and/or OCD
consistently exacerbate in temporal correlation to a GABHS infection.
The proposed pathophysiology of PANDAS begins with GABHS
infecting a susceptible host. An autoimmune reaction occurs, resulting in
production of brain tissue specific antistreptococcal antibodies, which
triggers an inflammatory response. The autoantibodies react with basal
ganglia proteins, particularly in the caudate nucleus and putamen.
Obsessions, compulsions, tics and other neuropsychiatric symptoms, arise
from interaction between these antibodies and neurons in the basal
ganglia via an unknown mechanism.
Egyptian children suffering from RF (with or without chorea) are
susceptible for PANDAS. Incidence of PANDAS is more in resistant
chorea patients (33%), with females being more affected. The most
common neuropsychiatric manifestations in this subgroup includes OCD
associated with ADHD, followed by OCD + tics + ADHD, then tics +
ADHD, and finally OCD + tics.
Swedo et al., 1998 proposed five diagnostic criteria:
1. The presence of OCD or a tic disorder or both.
2. Pediatric onset.
3. Episodic course of symptom severity with abrupt onset or dramatic
symptom exacerbations.
4. Temporal association with GABHS infection.
5. Association with neurological abnormalities during symptom
exacerbations.