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.

Psychomotor retardation



Total: 3

                       


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PMID (PMCID)
7125394
 MALE Infant
[Interstitial deletion of the long arms of chromosome 13].
Molina M, Santolaya JM, Onaindia ML, Sanchez E, De Garate J.
An Esp Pediatr. 1982;16(4):346-51.
We present a case of a child with important phenotypic abnormalities (retinoblastoma, hypoplasia of the thumbs and genital), as well as craneofacial and evident psychomotor retardation.
7391906
 MIXED_SAMPLE Infant, Newborn
Bilateral retinoblastoma with a 13qXp translocation.
Hida T, Kinoshita Y, Matsumoto R, Suzuki N, Tanaka H.
J Pediatr Ophthalmol Strabismus. 1980;17(3):144-6.
An infant girl suffering from bilateral retinoblastoma and psychomotor retardation with a translocation of the long arm of chromosome 13 to the short arm of the X chromosome was described.
910860
 MIXED_SAMPLE Infant, Newborn
Retinoblastoma in a patient with a 13qXp translocation.
Cross HE, Hansen RC, Morrow G 3rd, Davis JR.
Am J Ophthalmol. 1977;84(4):548-54.
The lack of other major organ malformations in this patient emphasized the importance of considering chromosomal aberrations as a possible etiology of retinoblastoma in patients with nonspecific psychomotor retardation.