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A Case of Meckel-Gruber Syndrome (Dysencephalia Splanchnocystica)
맥켈-그루버 증후군의 1예

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Authors
Chi, Je G.; Ko, Kyung Hyuk
Issue Date
1987-12
Publisher
Seoul National University College of Medicine
Citation
Seoul J Med 1987;28(4):379-381
Keywords
Meckel's syndromePolycystic kidneyEncephalocelePolydactylyCleft palate
Abstract
An autopsy case of Meckel's syndrome in a fetus is described. The brain
anomaly was detected on ultrasonography at 15 weeks of gestation and the pregnancy was
terminated at the gestation age of 21 weeks. No hereditary pattern was elicited in this case.
Multiple congenital anomalies consisted of posterior encephalocele with dysplastic brain, cleft
palate and lip without philtrum, postaxial polydactyly and syndactyly, polycystic kidneys of
Potter type III, fibrosis and bile duct proliferation of the liver, and interstitial fibrosis of the
pancreas and the spleen.
ISSN
0583-6802
Language
English
URI
http://hdl.handle.net/10371/6561
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Appears in Collections:
College of Medicine/School of Medicine (의과대학/대학원)Dept. of Medicine (의학과)The Seoul Journal of MedicineThe Seoul Journal of Medicine Vol. 28 No.4 (1987)
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