Associations of prenatally detected choroid plexus cysts with biochemical risk for congenital disorders
نویسندگان
چکیده
منابع مشابه
Choroid plexus cysts.
BACKGROUND Research shows that there is an association between choroid plexus cysts and aneuploidy. Family physicians treating prenatal patients should understand the management of this sonographic finding. OBJECTIVE To determine the epidemiology, pathophysiology, and management of prenatal choroid plexus cysts. CASE REPORT A 23-year-old patient, gravida 1, para 0, was seen at an inner city...
متن کاملChoroid plexus cysts and aneuploidy.
The association of choroid plexus cysts with fetal aneuploidy, particularly trisomy 18, was first noted in 1986. Through the years there have been numerous reports on this subject, but no consensus has been reached with regard to chromosomal risk. In this review, we attempt to summarise published reports on second trimester choroid plexus cysts, with an emphasis on the strengths and weaknesses ...
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Symptomatic cysts of the telencephalic choroid plexus are rare. This is a paediatric problem, with the oldest patient being 10 years old. Pertinent cases from the literature are reviewed. The case of a 9 year old girl with suboccipital headaches made more severe by lying on her right side or on her abdomen is discussed. Physical examination was within normal limits except for evidence of early ...
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At 33 weeks of pregnancy, a 29-year-old woman presented with uterine contractions. A transabdominal obstetrical sonogram with Doppler revealed severe hydrocephalus secondary to a large avascular third ventricular mass (Fig 1A). Delivery by cesarean section at 34 weeks revealed marked macrocephaly, widely separated sutures, and tense fontanelles. Contrast-enhanced computed tomography (CT) of the...
متن کاملBeals syndrome (Congenital contractural arachnodactly) with choroid plexus cyst
Beals syndrome or Congenital contractural arachnodactly (CCA) is an autosomal dominantly inherited connective tissue disorder caused by a mutation in FBN2 gene on chromosome 5q23 and is characterized by multiple flexion contractures, arachnodactyly, severe kyphoscoliosis, abnormal pinna and muscular hypoplasia. Multiple joint contractures (especially finger joints), and crumpled ears in the abs...
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ژورنال
عنوان ژورنال: Medical Studies
سال: 2014
ISSN: 1899-1874
DOI: 10.5114/ms.2014.43593