Literature DB >> 3587887

Activity of red cell esterase D in 50 cases of retinoblastoma patients and their family members.

K Fujiki, Y Kuwabara, A Nakajima, I Nishigaki, T Ikeuchi.   

Abstract

Esterase D was qualitatively and quantitatively analyzed in the red blood cells from 50 retinoblastoma patients who had been followed-up at Juntendo University and their family. In only one case with deletion of chromosome No. 13 (q12.3-q21.2), was the esterase D activity (type 2) 1.47 Unit/gHb which was approximately 50% of the level in normals. Additional retinoblastoma patients and their family members, 77 parents and 25 siblings, showed a normal range of esterase D level in their own phenotypes. These facts confirmed that the deletion of an esterase D locus was infrequent (approximately 2% in our series) in retinoblastoma patients. It was also compatible with the published data that the range of deletion of chromosome was No. 13 (q12.3-q21.2) involving 13q14.

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Year:  1987        PMID: 3587887     DOI: 10.3109/13816818709028510

Source DB:  PubMed          Journal:  Ophthalmic Paediatr Genet        ISSN: 0167-6784


  1 in total

1.  Types, rates, origin and expressivity of chromosome mutations involving 13q14 in retinoblastoma patients.

Authors:  Y Ejima; M S Sasaki; A Kaneko; H Tanooka
Journal:  Hum Genet       Date:  1988-06       Impact factor: 4.132

  1 in total

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