Meckel-Gruber Syndrome: An autopsy case report
Korean Journal of Pathology
; : 200-202, 1994.
Article
в Ko
| WPRIM
| ID: wpr-46759
Ответственная библиотека:
WPRO
ABSTRACT
Meckel-Gruber syndrome is a quite rare congenital disorder, characterized by posterior encepalocele, cleft palate and lip, polycystic kidneys, hepatic fibrosis with bile duct proliferation, and postaxial polydactyly and syndactyly. We experienced an autopsy case of M eckel-Gruber syndrome in a second baby of 28 year-old woman. At 26 weeks of gestation, congenital anomaly was detected on ultrasonographic examination and the pregnancy was terminated. Familial history was not noted.
Key words
Полный текст:
1
База данных:
WPRIM
Пределы темы:
Female
/
Humans
/
Pregnancy
Язык:
Ko
Журнал:
Korean Journal of Pathology
Год:
1994
Тип:
Article