Aniridia--Wilms' tumour association--a case with 11p 13-14.1 deletion and ventricular septal defect.
Indian J Cancer
;
1992 Sep; 29(3): 117-21
Article
in English
| IMSEAR
| ID: sea-50810
ABSTRACT
A two year old female child with bilateral wilms tumor (WT) along with multiple congenital anomalies like bilateral aniridia with congenital cataracts and nystagmus, microcephaly, mental retardation and ventricular septal defect has been described. The karyotype analysis revealed 46 xx, del 11p 13-14.1. Association of ventricular septal defect with the classical features of 'Aniridia-Wilms' tumor association' is an unusual feature in this case.
Full text:
Available
Index:
IMSEAR (South-East Asia)
Main subject:
Chromosomes, Human, Pair 11
/
Female
/
Humans
/
Aniridia
/
Child, Preschool
/
Chromosome Deletion
/
Wilms Tumor
/
Heart Septal Defects, Ventricular
/
Karyotyping
Language:
English
Journal:
Indian J Cancer
Year:
1992
Type:
Article
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