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Meckel-Gruber syndrome: a lethal combination of abnormalities
West Indian med. j ; 39(1): 52-6, mar. 1990. tab
Article in En | LILACS | ID: lil-87914
Responsible library: BR1.1
ABSTRACT
We herein describe two cases of Meckel-Gruber Syndrome identified in stilborn infants. Both had all three elements of the classical triad, namely, occipital encephalocele, renal cystic dysplasia and post-axial polydactyly. In addition, many of the other well-known accompanying abnormalities were present. Awareness of this entity in this region is important because of its high risk of recurrence in subsequent pregnancies
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Index: LILACS Main subject: Encephalocele / Fingers / Polycystic Kidney Diseases Type of study: Diagnostic_studies / Prognostic_studies Limits: Female / Humans / Infant / Newborn / Pregnancy Language: En Journal: West Indian med. j Journal subject: MEDICINA Year: 1990 Type: Article
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Index: LILACS Main subject: Encephalocele / Fingers / Polycystic Kidney Diseases Type of study: Diagnostic_studies / Prognostic_studies Limits: Female / Humans / Infant / Newborn / Pregnancy Language: En Journal: West Indian med. j Journal subject: MEDICINA Year: 1990 Type: Article