Our policy in diagnosis and treatment of hydrocephalus
✍ Scribed by Zsolt Kopniczky; Pál Barzó; László Pávics; Tamás Dóczi; Mihály Bodosi; László Csernay
- Publisher
- Springer
- Year
- 1995
- Tongue
- English
- Weight
- 362 KB
- Volume
- 11
- Category
- Article
- ISSN
- 0256-7040
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Since the description of X-linked hydrocephalus by Bickers and Adams in 1949,' genetic counseling concerning this disease has benefited from the addition of prenatal ultrasound examinations, and more recently from the progress made in genetic engineering.2 We are reporting on a case in which sonogra
Instead of the usual descriptive criteria commonly adopted for angiographic assessment of hydrostatic hydrocephalus, planimetric measuring methods were tried out. It was shown that the surface area under the anterior cerebral artery (pericallosal) as measured in the lateral angiogram increases propo
A patient with ring chromosome 6/monosomy 6 mosaicism is presented. At 25 weeks' gestation, ultrasound examination demonstrated fetal hydrocephalus. Amniocentesis was performed. The fetal karyotype was 45,XY, -61 45,XY, -6,+f/46,XY,r(6)(p25q27). Delivery of this male infant was by Caesarean section
The prenatal diagnosis of hydrocephalus is described in 11 cases between 17 and 21 weeks using two sonographic criteria. These sonographic findings involve the asymmetrical appearance of the choroid plexus and the size and configuration of the anterior horns of the lateral ventricles. We have found