Dandy Walker Variant and Bipolar I Disorder with Graphomania

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Dandy Walker Variant and Bipolar I Disorder with Graphomania

Cerebellum is known to play an important role in coordination and motor functions. In some resent studies it is also considered to be involved in modulation of mood, cognition and psychiatric disorders. Dandy Walker Malformation is a congenital malformation that is characterized by hypoplasia or aplasia of the cerebellar vermis, cystic dilatation of the fourth ventricle and enlargement of the p...

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Bipolar Disorder in a Young Girl with Dandy-Walker Syndrome

corresponding author Fariborz Estilaee, Department of Psychiatry, Neyshabur University of Medical Sciences, Neyshabur, Iran. Adress:22 Bahman Hospital, Neyshabur,Iran. Tel: 098-9155512181 Email:[email protected] Dandy-Walker syndrome is a congenital brain malformation involving the cerebellum and the fourth ventricle. The key features of this syndrome are mental retardation, cerebellar ataxia,...

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bipolar disorder in a young girl with dandy-walker syndrome

dandy-walker syndrome is a congenital brain malformation involving the cerebellum and the fourth ventricle. the key features of this syndrome are mental retardation, cerebellar ataxia, and symptoms related to hydrocephaly. the psychiatric aspects of this syndrome have been insufficiently appreciated. described here is a 17- year- old girl with an acute manic episode emerged in the course of dan...

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The Coexistence of Gonadal Dysgenesis With Mayer-rokitansky-küster-hauser Syndrome, and Dandy-Walker Variant

Background: Gonadal dysgenesis, the most common cause of primary amenorrhea, is characterized by absent or underdeveloped ovaries. Although the coexistence of gonadal dysgenesis and Mayer-Rokitansky-Küster-Hauser (MRKH) has been reported, it is still quite infrequent. To the extent that authors searched, just one study reported the association between Rokitansky sequence and Dandy-Walker malfor...

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Aplasia of the Internal Carotid Artery with Dandy-Walker Variant.

Dear Editor, A 28-year-old woman presented with a 2-year history of headache, and magnetic resonance imaging (MRI) led to a diagnosis of suspected intracranial malformation. She had been in good health and had developed normally prior to developing the symptom. A neurological examination on admission revealed no anomaly. Brain MRI revealed agenesis of the inferior part of cerebellar vermis and ...

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ژورنال

عنوان ژورنال: Psychiatry Investigation

سال: 2014

ISSN: 1738-3684,1976-3026

DOI: 10.4306/pi.2014.11.3.336