ISSN:
1433-0350
Schlagwort(e):
Key words Holoprosencephaly
;
Craniofacial malformations
;
Epilepsy
;
Survival
Quelle:
Springer Online Journal Archives 1860-2000
Thema:
Medizin
Notizen:
Abstract Alobar holoprosencephaly is one of the most severe congenital malformations of the central nervous system. Most affected infants are stillborn or have a very short life-span. The survivors can present with neonatal seizures and/or infantile spasms. We report on an unusually long-lived patient with alobar holoprosencephaly and minor facial dysmorphism, who developed generalized epilepsy during childhood.
Materialart:
Digitale Medien
URL:
http://dx.doi.org/10.1007/s003810050392
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