P27.06: Prenatal diagnosis of schizencephaly Type II in 2 cases
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...
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OBJECTIVE To characterize the prenatal sonographic features of osteogenesis imperfecta (OI) type II. DESIGN Descriptive (case series). SETTING Department of Obstetrics and Gynecology, Faculty of Medicine, Maharaj Nakorn Chiang Mai Hospital, Chiang Mai University. SUBJECTS Six fetuses with prenatal diagnosis of OI were evaluated. RESULTS Six fetuses were prenatally diagnosed as OI type I...
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leukocyte adhesion deficiency type-1(lad-1) is one of the autosomal recessive immunodeficiency diseases that results from mutation in integrin beta 2 (itgb2) gene. the aim of this study was to investigate molecular prenatal diagnosis of lad-1. four pregnant women with five fetuses (one twin fetus) with clinical and laboratory diagnosis of lad-1 in their previous children were studied. the chori...
متن کاملCorrelation of prenatal and postnatal MRI findings in schizencephaly.
BACKGROUND AND PURPOSE Schizencephaly is a rare malformation of the brain characterized by a gray matter-lined defect extending from the pial surface to the lateral ventricles. The purpose of this study was to correlate imaging findings of schizencephaly and associated anomalies on fetal and postnatal MR imaging and assess possible changes that may occur from the prenatal-to-postnatal state. ...
متن کاملTWO CASES OF TYROSINEMIA TYPE II, AND ITS RARE OCCURRENCE IN TWO BROTHERS
Tyrosinemia type II is a rare autosomal recessive disorder wich can present itself with recurrent epithelial keratitis, hyperkeratotic skin lesions and mental retardation. This article reports the rare occurrence of this disease in both offsprings (two brothers) of a family (consanguinous'marriage) who were managed with a lowprotein diet and a special regimen.
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ژورنال
عنوان ژورنال: Ultrasound in Obstetrics and Gynecology
سال: 2008
ISSN: 0960-7692,1469-0705
DOI: 10.1002/uog.5936