Laryngospasm as a single manifestation of epilepsy
نویسندگان
چکیده
منابع مشابه
Laryngospasm as a single manifestation of epilepsy.
The presence in the hepatic granulomas of eosinophils raised the possibility of Toxocara infestation. Larval remnants were not present within the granulomas nor was there peripheral eosinophilia or any other manifestation of larval migration-for example chorioretinitis. Although there are numerous causes of hepatic granulomas the liver in this case showed features previously reported in extensi...
متن کاملepilepsy as a rare neurologic manifestation of oculodentodigitalis dysplasia
how to cite this article: barzegar m, sayadnasiri m, tabrizi a. epilepsy as a rare neurologic manifestation of oculodentodigitalis dysplasia. iran j child neurol 2012; 6(3): 39-43. oculodentodigitalis dysplasia (oddd) is an extremely rare inherited disorderinvolving the development of the face, eyes, teeth and limbs. in addition,some patients develop neurological problems mostly a spastic parap...
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Background: Multiple sclerosis (MS) is an inflammatory and demyelinating disease of central nervous system (CNS). The aim of the present study was to determine the type and the frequency of initial presenting symptoms in patients with MS and their relation with demographic characteristics in Babol, northern Iran. Methods: All patients of this study were recruited over a ten year period fr...
متن کاملTemporal lobe epilepsy as a unique manifestation of multiple sclerosis.
OBJECTIVE To report on five patients with temporal lobe epilepsy (TLE) as the unique manifestation of multiple sclerosis (MS). METHODS Among 350 consecutive MS patients, we identified 16/350 (4.6%) who also had epileptic seizures. Here, we review their electrophysiological and clinical features. RESULTS Five of these 16 patients (four female, one male; mean age 34.2 years; range 31 to 38) w...
متن کاملEpilepsy as a Rare Neurologic Manifestation of Oculodentodigitalis Dysplasia
Oculodentodigitalis dysplasia (ODDD) is an extremely rare inherited disorder involving the development of the face, eyes, teeth and limbs. In addition, some patients develop neurological problems mostly a spastic paraparesis associated with white matter abnormalities on magnetic resonance imaging. This report describes a patient with epilepsy, a rare neurologic manifestation of this syndrome.
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ژورنال
عنوان ژورنال: Archives of Disease in Childhood
سال: 1983
ISSN: 0003-9888,1468-2044
DOI: 10.1136/adc.58.2.151