Schizencephaly and Psychosis: A Rare Association
نویسندگان
چکیده
منابع مشابه
Schizencephaly and Psychosis: A Rare Association
Schizencephaly is a rare malformation of the central nervous system defined as a gray matter-lined cleft filled with cerebrospinal fluid that extends from the pial surface to the ventricle. Few cases of association with psychosis were reported in the scientific literature. We present a case of a 46-year-old woman, admitted into a psychiatric hospital with crises of psychomotor agitation, disorg...
متن کاملSHORT REPORT Schizencephaly associated with psychosis
Schizencephaly is a rare disorder of brain development resulting in the formation of abnormal unilateral or bilateral clefts in the cerebral hemispheres. It is often accompanied by partial seizures, mental retardation, and hemiparesis. Two patients are described with clear psychotic symptoms with either unilateral or bilateral schizencephaly. The implications of the association between schizenc...
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Sheehan’s syndrome (SS) refers to the occurrence of varying degree of hypopituitarism after parturition (1). It is a rare cause of hypopituitarism in developed countries owing to advances in obstetric care and its frequency is decreasing worldwide. However, it is still frequent in underdeveloped and developing countries. Sheehan’s syndrome is often diagnosed late as it evolves slowly (2,3). Re...
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An 820 g, 28 week , small-for-gestational-age boy was born after an uneventful but shortened pregnancy. At birth , the circumference of the infant's head (23 cm) was well below the third percentile. Transillumination of the skull was increased over the parietotemporal areas bilaterally. Initially, he had minimal spontaneous movements, little response to stimulation, absent suck reflex , minimal...
متن کاملFamilial schizencephaly: further delineation of a rare disorder.
We report on two Somalian sibs with severe developmental retardation and spastic cerebral paresis. Both children have bilateral cerebral clefts in the Sylvian region with dilatation of the ventricles, absence of the septum pellucidum, and heterotopia. The diagnosis of familial schizencephaly was made. The occurrence of schizencephaly in two affected sibs supports a genetic basis for schizenceph...
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ژورنال
عنوان ژورنال: Case Reports in Medicine
سال: 2013
ISSN: 1687-9627,1687-9635
DOI: 10.1155/2013/210868