Bilateral schizencephaly Type II
نویسندگان
چکیده
منابع مشابه
Bilateral schizencephaly Type II.
BACKGROUND Schizencephaly is one of the most severe forms of neuronal migration defects and is an extremely rare cause of seizure disorder. CASE DETAILS We report a case of bilateral schizencephaly (Type II) presenting as seizure disorder since birth. DISCUSSION This case is rare because of the relatively benign features compared to other reported cases. CONCLUSION Compared to other cases...
متن کاملSchizencephaly associated with bipolar II disorder.
A 55-year-old man with congenital hemiparesis of the right side, three episodes of generalised tonic-clonic seizure at 16 years of age, and two episodes of severe depression and two episodes of hypomania in the past, presented with severe depression with psychotic symptoms. Computed tomography of the brain showed a grey matter-lined cerebrospinal fluid-filled cleft in the left cerebral hemisphe...
متن کاملPersistent bilateral proatlantal type II artery.
Vascular anomalies and variants are common in patients undergoing imaging studies, and patients with these anomalies are generally asymptomatic. Remnants of fetal carotid-basilar circulation are rarely identified. We report a rare case of persistent type 2 bilateral proatlantal arteries, in which the patient presented with dizziness.
متن کاملSchizencephaly. .
45 melanin, but also slow nail growth rate resulting in larger accumulation of the pigment. The presence of HHN neither correlates with degree of renal impairment nor with blood urea nitrogen or creatinine levels. HHN can be an important clue in making the diagnosis of renal disease. 3 0 year old male presented with history of generalised tonic clonic seizures since the age of 16 poorly control...
متن کاملA case of congenital bilateral perisylvian syndrome due to bilateral schizencephaly.
A case of congenital bilateral perisylvian syndrome (CBPS) associated with bilateral perisylvian schizencephaly in a 24-year-old woman is reported. She presented the classical clinical triad of CBPS, which included congenital facio-masticatory diplegia, epilepsy and only mild mental retardation, despite the presence of bilateral, open-lip clefts in the perisylvian region. We hypothesize that th...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Australasian Medical Journal
سال: 2014
ISSN: 1836-1935
DOI: 10.4066/amj.2014.1924