Retinoblastoma

A rare eye tumor disease representing the most common intraocular malignancy in children. It is a life threatening neoplasia but is potentially curable and it can be hereditary or non hereditary, unilateral or bilateral.

Aniridia

Abnormality of the iris characterized by, typically bilateral, complete or partial iris hypoplasia. The phenotype ranges from mild defects of anterior iris stroma only to almost complete absence of the iris.


Total: 7

                       


(per page)
PMID (PMCID)
7977618
 MALE Infant
Association and chance occurrence of aniridia and retinoblastoma.
To KW, Mukai S, Friedman AH.
Am J Ophthalmol. 1994;118(6):820-2.
Family history disclosed three generations of aniridia; yet there were no instances of retinoblastoma.
7977618
 MALE Infant
Association and chance occurrence of aniridia and retinoblastoma.
To KW, Mukai S, Friedman AH.
Am J Ophthalmol. 1994;118(6):820-2.
A 9-month-old infant had inherited aniridia and unilateral retinoblastoma.
7977618
 MALE Infant
Association and chance occurrence of aniridia and retinoblastoma.
To KW, Mukai S, Friedman AH.
Am J Ophthalmol. 1994;118(6):820-2.
Association and chance occurrence of aniridia and retinoblastoma.
7977618
 MALE Infant
Association and chance occurrence of aniridia and retinoblastoma.
To KW, Mukai S, Friedman AH.
Am J Ophthalmol. 1994;118(6):820-2.
The coincidental occurrence of retinoblastoma and aniridia is rare.
7977618
 MALE Infant
Association and chance occurrence of aniridia and retinoblastoma.
To KW, Mukai S, Friedman AH.
Am J Ophthalmol. 1994;118(6):820-2.
With DNA probes from within the retinoblastoma gene, we were able to determine that a retinoblastoma-predisposing mutation was not inherited with aniridia in this family.
7977618
 MALE Infant
Association and chance occurrence of aniridia and retinoblastoma.
To KW, Mukai S, Friedman AH.
Am J Ophthalmol. 1994;118(6):820-2.
With DNA probes from within the retinoblastoma gene, we were able to determine that a retinoblastoma-predisposing mutation was not inherited with aniridia in this family.
225131
 MALE Child
Aniridia-Wilms' tumor association: evidence for specific deletion of 11p13.
Francke U, Holmes LB, Atkins L, Riccardi VM.
Cytogenet Cell Genet. 1979;24(3):185-92.
Possible relationships between heterozygous deletion of specific chromosomal bands 11p13 and 13q14 and the autosomal dominant disorders aniridia, Wilms' tumor, and retinoblastoma, respectively, are discussed.