ISSN:
1433-0350
Schlagwort(e):
Key words Meckel-Gruber syndrome
;
Encephalocele
;
Hydrocephaly
Quelle:
Springer Online Journal Archives 1860-2000
Thema:
Medizin
Notizen:
Abstract Meckel-Gruber syndrome is a congenital disorder characterized by occipital encephalocele, polydactyly and polycystic kidneys. This rare syndrome has been reported in the literature as incompatible with life. We present the case of a newborn afflicted with the clinical triad of Meckel-Gruber syndrome. Appropriate treatment instituted in our case led to a good early outcome.
Materialart:
Digitale Medien
URL:
http://dx.doi.org/10.1007/s003810050198
Permalink