Literature DB >> 6885051

A recognizable pattern of the midface of retinoblastoma patients with interstitial deletion of 13q.

T Motegi, M Kaga, Y Yanagawa, H Kadowaki, K Watanabe, A Inoue, M Komatsu, K Minoda.   

Abstract

In our study, we found a recognizable pattern of the midface in three retinoblastoma patients with interstitial deletion of chromosome 13 in lymphocytes. Further photographs of patients reported by other authors confirmed our conclusion that the midface in children with interstitial deletion of 13q from q12 to q22, always involving q14, is characterized by prominent eyebrows, broad nasal bridge, bulbous tip of the nose, a large mouth with a thin upper lip, and a long philtrum. This midface pattern could not be recognized in patients with normal karyotypes, suggesting that the critical segment for the midface phenotype as well as for retinoblastoma may exist in band 13q14.

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Year:  1983        PMID: 6885051     DOI: 10.1007/bf00327116

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  12 in total

1.  Chromosomal anomalies in patients with retinoblastoma.

Authors:  M G Wilson; A J Ebbin; J W Towner; W H Spencer
Journal:  Clin Genet       Date:  1977-07       Impact factor: 4.438

2.  Retinoblastoma and D-chromosome deletions.

Authors:  M G Wilson; J W Towner; A Fujimoto
Journal:  Am J Hum Genet       Date:  1973-01       Impact factor: 11.025

3.  Retinoblastoma and long arm delection of chromosome 13. Attempts to define the deleted segment.

Authors:  E Orye; M J Delbeke; B Vandenabeele
Journal:  Clin Genet       Date:  1974       Impact factor: 4.438

4.  Retinoblastoma and deletion D (14) syndrome.

Authors:  M G Wilson; J Melnyk; J W Towner
Journal:  J Med Genet       Date:  1969-09       Impact factor: 6.318

5.  Confirmation of regional assignment of gene for human esterase-D to chromosome band 13q14.

Authors:  J J Hoo; M Koch; B Ziemsen; W Foerster; I Nishigaki
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

6.  Lymphocyte chromosome survey in 42 patients with retinoblastoma: effort to detect 13q14 deletion mosaicism.

Authors:  T Motegi
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

7.  High rate of detection of 13q14 deletion mosaicism among retinoblastoma patients (using more extensive methods).

Authors:  T Motegi
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

8.  Sporadic bilateral retinoblastoma and 13q- chromosomal deletion.

Authors:  U Francke; F Kung
Journal:  Med Pediatr Oncol       Date:  1976

9.  [Retinoblastoma and interstitial deletion of 13q (author's transl)].

Authors:  J De Grouchy; C Turleau; M O Cabanis; J M Richardet
Journal:  Arch Fr Pediatr       Date:  1980-10

10.  Partial triplication and deletion of 13q: study of a family presenting with bilateral retinoblastomas.

Authors:  V M Riccardi; H M Hittner; U Francke; S Pippin; G P Holmquist; F L Kretzer; R Ferrell
Journal:  Clin Genet       Date:  1979-04       Impact factor: 4.438

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  13 in total

Review 1.  13q13.1-q13.2 deletion in tetralogy of Fallot: clinical report and a literature review.

Authors:  Gregory Costain; Candice K Silversides; Christian R Marshall; Mary Shago; Nicholas Costain; Anne S Bassett
Journal:  Int J Cardiol       Date:  2010-07-03       Impact factor: 4.164

2.  Congenital anomalies and childhood cancer in Great Britain.

Authors:  S A Narod; M M Hawkins; C M Robertson; C A Stiller
Journal:  Am J Hum Genet       Date:  1997-03       Impact factor: 11.025

3.  Bilateral retinoblastoma in a male patient with an X; 13 translocation: evidence for silencing of the RB1 gene by the spreading of X inactivation.

Authors:  C Jones; C Booth; D Rita; L Jazmines; B Brandt; A Newlan; B Horsthemke
Journal:  Am J Hum Genet       Date:  1997-06       Impact factor: 11.025

4.  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

5.  Isolation and characterisation of a panel of cosmids which allows unequivocal identification of chromosome deletions involving the RB1 gene using fluorescence in situ hybridisation.

Authors:  J K Cowell; R Jaju; H Kempski
Journal:  J Med Genet       Date:  1994-04       Impact factor: 6.318

6.  Genotype-phenotype correlations in patients with retinoblastoma and interstitial 13q deletions.

Authors:  Diana Mitter; Reinhard Ullmann; Artur Muradyan; Ludger Klein-Hitpass; Deniz Kanber; Katrin Ounap; Marc Kaulisch; Dietmar Lohmann
Journal:  Eur J Hum Genet       Date:  2011-04-20       Impact factor: 4.246

7.  Familial retinoblastoma (mother and son) with 13q14 deletion.

Authors:  Y Fukushima; Y Kuroki; T Ito; I Kondo; I Nishigaki
Journal:  Hum Genet       Date:  1987-10       Impact factor: 4.132

8.  De novo complex autosomal translocation involving chromosomes 8, 13 and 15 in a girl with a sporadic retinoblastoma.

Authors:  E Calzolari; P Palazzi; V Aiello; E Mazzeo; P Perri; A Minelli; L del Senno; P Patracchini; F Bernardi
Journal:  Hum Genet       Date:  1987-09       Impact factor: 4.132

Review 9.  Retinoblastoma and Neuroblastoma Predisposition and Surveillance.

Authors:  Junne Kamihara; Franck Bourdeaut; William D Foulkes; Jan J Molenaar; Yaël P Mossé; Akira Nakagawara; Andreu Parareda; Sarah R Scollon; Kami Wolfe Schneider; Alison H Skalet; Lisa J States; Michael F Walsh; Lisa R Diller; Garrett M Brodeur
Journal:  Clin Cancer Res       Date:  2017-07-01       Impact factor: 12.531

10.  Retinoblastoma and mental retardation microdeletion syndrome: clinical characterization and molecular dissection using array CGH.

Authors:  R Caselli; C Speciale; C Pescucci; V Uliana; K Sampieri; M Bruttini; I Longo; S De Francesco; T Pramparo; O Zuffardi; R Frezzotti; A Acquaviva; T Hadjistilianou; A Renieri; F Mari
Journal:  J Hum Genet       Date:  2007-05-15       Impact factor: 3.172

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