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Case Report
Magnetic Resonance Angiography in One Case of Hydraencephaly
Eun Kyung Hwang, Kang Ho Cho, Gwang Hoon Lee, Gil Hyun Kim, Hak Soo Lee, Ji Hye Kim, Young Seok Lee
Clin Exp Pediatr. 1998;41(4):538-542.   Published online April 15, 1998
In hydranencephaly, the cerebral hemispheres are absent or represented by membranous sacs with remnants of frontal, temporal or occipital cortex dispersed over the membrane. The brain stem is relatively intact. The cause of hydranencephaly is unknown, but bilateral occlusion of the internal carotid arteries during early fetal development can explain most of the pathologic abnormalities. We evaluated a case of hydranencephaly by magnetic resonance(MR)...
A Case of Hydranencephaly Combined with Twin Pregnancy
Hong Ju Choi, Jin Kil Park, Hee Tag Lim, Jae Sam Kim, Hyo Kyung Sin, Chul Hoi Gu, Son Young Lee
Clin Exp Pediatr. 1994;37(4):547-552.   Published online April 15, 1994
Hydranencehaly is an abnormality consisting of complete or almost absence of the cerebral hemispheres, which are replaced by a large fluid-filled cavity. The midbrain and brain stem are relatively intact, and rudiments of frontal, temporal and occipital cortex may be present. We diagnosed it through the evaluation of clinical features, prenatal US (intrauterine pregnancy, 37 wks) and brain CT. Authors have experienced...
Original Article
A Case of Hydranencephaly.
Min Cheol Kim, Moon Ja Park, Kong Sik Kim, Kyeong Rae Moon, Yeong Bong Park
Clin Exp Pediatr. 1989;32(12):1752-1756.   Published online December 31, 1989
Hydranencephaly is congenital absence of the cerebral hemispheres, which are replaced by a large, fluid-filled cavity. The brain stem and basal ganglia are well formed, and rudients of frontal & occipital cortex may be present. We experienced a cases of hydranencephaly in a 6 month-old male infant who had not haven visual following and head control. We diagnosed it through the evaluation of clinical features,...
Case Report
An Autopsy Report of a Hydranencephaly.
J K Park, Y J Kim, T J Hwang
Clin Exp Pediatr. 1984;27(3):293-296.   Published online March 31, 1984
A case of hydranencephalic male, who was delivered in prematurity at Chonnam University Hospital and had lived for 41 days after birth, was presented. The pathologic and anatomical findings were hypoplasia of brain cortex, 3rd and lateral ventricles, atresia of the aqueduct of Sylvius and accumulation of 430ml of yellowish fluid in cranial cavity. No associated congenital anomalies of adrenal...
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