Literature DB >> 6246230

Familial occurrence of the aniridia-Wilms tumor syndrome with deletion 11p13-14.1.

J J Yunis, N K Ramsay.   

Abstract

A report of a family with two half-brothers and a maternal aunt affected with the aniridia-Wilms tumor syndrome is presented. The proband showed a deletion of most of band 11p13 and of subband 11p14.1 of one chromosome 11, and the proband's mother and an older brother, both phenotypically normal, showed a balanced chromosomal rearrangement. This family demonstrates that deletion of a small chromosome segment (11p13-14.1) is responsible for the aniridia-Wilms tumor syndrome and, that in some cases, the syndrome can be familial.

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Year:  1980        PMID: 6246230     DOI: 10.1016/s0022-3476(80)80630-5

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  25 in total

Review 1.  Wilms' and associated renal tumors of childhood.

Authors:  K S White; H Grossman
Journal:  Pediatr Radiol       Date:  1991

2.  [Terminal renal failure in aniridia-Wilms syndrome].

Authors:  H Wilms; E Back; G Kirste
Journal:  Klin Wochenschr       Date:  1986-09-01

3.  Familial isolated aniridia associated with a translocation involving chromosomes 11 and 22 [t(11;22)(p13;q12.2)].

Authors:  J W Moore; S Hyman; S E Antonarakis; E H Mules; G H Thomas
Journal:  Hum Genet       Date:  1986-04       Impact factor: 4.132

Review 4.  Microcytogenetics 1984.

Authors:  J de Grouchy; C Turleau
Journal:  Experientia       Date:  1986-10-15

5.  Linkage analysis of a DNA marker localized to 20p12 and multiple endocrine neoplasia type 2A.

Authors:  P J Goodfellow; B N White; J J Holden; A M Duncan; E V Sears; H S Wang; L Berlin; K K Kidd; N E Simpson
Journal:  Am J Hum Genet       Date:  1985-09       Impact factor: 11.025

6.  Regional mapping of catalase and Wilms tumor--aniridia, genitourinary abnormalities, and mental retardation triad loci to the chromosome segment 11p1305----p1306.

Authors:  K Narahara; K Kikkawa; S Kimira; H Kimoto; M Ogata; R Kasai; M Hamawaki; K Matsuoka
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

7.  Wilms' tumor, malformative syndrome, mental retardation and de novo constitutional translocation, t(7;13)(q36;q13).

Authors:  J L Bernard; M A Baeteman; J F Mattei; C Raybaud; F Giraud
Journal:  Eur J Pediatr       Date:  1984-01       Impact factor: 3.183

8.  High-resolution studies in patients with aniridia-Wilms tumor association, Wilms tumor or related congenital abnormalities.

Authors:  Y Nakagome; T Ise; M Sakurai; T Nakajo; E Okamoto; T Takano; Y Nakahori; Y Tsuchida; N Nagahara; Y Takada
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

9.  Wilms's tumour and aniridia: clinical and cytogenetic features.

Authors:  R S Shannon; J R Mann; E Harper; D G Harnden; J E Morten; A Herbert
Journal:  Arch Dis Child       Date:  1982-09       Impact factor: 3.791

10.  Chromosome 20 deletion in human multiple endocrine neoplasia types 2A and 2B: a double-blind study.

Authors:  V R Babu; D L Van Dyke; C E Jackson
Journal:  Proc Natl Acad Sci U S A       Date:  1984-04       Impact factor: 11.205

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