ISSN:
1432-1076
Schlagwort(e):
Chromosomal aberration
;
Ring chromosome 15
;
Dysplasias
;
Malformations
;
Ventricular septal defect
Quelle:
Springer Online Journal Archives 1860-2000
Thema:
Medizin
Notizen:
Abstract A 20-day-old female neonate was admitted with symptoms caused by a large ventricular septal defect which was subsequently confirmed angiographically. Other clinical findings were pre-and postnatal growth retardation, microcephaly, dysmorphism of ears, fingers and feet. Cytogenetic analysis revealed a ring chromosome 15. Despite a palliative banding operation of the pulmonary artery, the infant succumbed to complications of her congenital heart disease in the 4th month of life.
Materialart:
Digitale Medien
URL:
http://dx.doi.org/10.1007/BF00442457
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