Sturge-Weber syndrome-A Case report.

dc.contributor.authorHalim, Abdul
dc.contributor.authorAlam, Md Towhid
dc.contributor.authorBarman, R C
dc.date.accessioned2016-02-13T08:37:40Z
dc.date.available2016-02-13T08:37:40Z
dc.date.issued2013-01
dc.description.abstractSturge-weber syndrome is a disease characterized by capillary or cavernous haemangionsm (Port-wine stain) along the cutaneous division of Trigennial nerve. There is venous haemangionsm in subjacent leptomeninges, which may spread causing atrophy of cortex. The patient Md. Zobair Hossain, 11 years old boy, nondiabetic, nonhypertensive presented to us on 20.05.2011 with the complaints of repeated bleeding from a swelling over the outer aspect of right eye ball for 1 month, weakness of left half of body for 1 year and repeated convulsion for 7 years. Diagnosis was confirmed vy CT scan of brain. Through treatment is unsatisfactory, he was advised for laser theraphy for coetaneous lesion and anti-convulsant drug epilepsy.en_US
dc.identifier.citationHalim Abdul, Alam Md Towhid, Barman R C. Sturge-Weber syndrome-A Case report. Faridpur Medical College Journal. 2013 Jan; 8(1): 44-45.en_US
dc.identifier.issn2079-3553
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/172749
dc.language.isoenen_US
dc.source.urihttps://www.banglajol.info/index.php/FMCJ/article/view/16899en_US
dc.subjectSturge-weberen_US
dc.subjectsyndromeen_US
dc.subjectcuntaneous haemangiomaen_US
dc.subjectleft sided hemipleginen_US
dc.subjectepilepsyen_US
dc.subjectintracranial calcificationen_US
dc.titleSturge-Weber syndrome-A Case report.en_US
dc.typeArticleen_US
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