Electroconvulsive Therapy and Corpus Callosum Aplasia : A 3-Year Followup

المؤلفون المشاركون

Strauss, Philipp
Pogarell, Oliver
Born, Christoph
Palm, Ulrich

المصدر

Case Reports in Psychiatry

العدد

المجلد 2011، العدد 2011 (31 ديسمبر/كانون الأول 2011)، ص ص. 1-2، 2ص.

الناشر

Hindawi Publishing Corporation

تاريخ النشر

2011-10-31

دولة النشر

مصر

عدد الصفحات

2

التخصصات الرئيسية

علم النفس
الطب النفسي

الملخص EN

Electroconvulsive Therapy (ECT) is a powerful treatment option in severe or chronic catatonic states and has been reported to be useful in oligophrenic patients.

We report the followup medical history of a patient with corpus callosum aplasia (or agenesis) who was continuously treated with ECT over three years.

First, he improved considerably after a series of ECT, but relapses of catatonia made a continuous, weekly ECT necessary.

Due to the severity of the brain malformation, an add-on medication with benzodiazepines and second generation antipsychotics was necessary to treat catatonic symptoms.

This case emphasises the benefits of long-term ECT in oligophrenic patients.

نمط استشهاد جمعية علماء النفس الأمريكية (APA)

Palm, Ulrich& Strauss, Philipp& Born, Christoph& Pogarell, Oliver. 2011. Electroconvulsive Therapy and Corpus Callosum Aplasia : A 3-Year Followup. Case Reports in Psychiatry،Vol. 2011, no. 2011, pp.1-2.
https://search.emarefa.net/detail/BIM-487254

نمط استشهاد الجمعية الأمريكية للغات الحديثة (MLA)

Palm, Ulrich…[et al.]. Electroconvulsive Therapy and Corpus Callosum Aplasia : A 3-Year Followup. Case Reports in Psychiatry No. 2011 (2011), pp.1-2.
https://search.emarefa.net/detail/BIM-487254

نمط استشهاد الجمعية الطبية الأمريكية (AMA)

Palm, Ulrich& Strauss, Philipp& Born, Christoph& Pogarell, Oliver. Electroconvulsive Therapy and Corpus Callosum Aplasia : A 3-Year Followup. Case Reports in Psychiatry. 2011. Vol. 2011, no. 2011, pp.1-2.
https://search.emarefa.net/detail/BIM-487254

نوع البيانات

مقالات

لغة النص

الإنجليزية

الملاحظات

Includes bibliographical references

رقم السجل

BIM-487254