Literature DB >> 3184142

Deletion of a single chromosome band 4q26 in a malformed girl: exclusion of Rieger syndrome associated gene(s) from the 4q26 segment.

T Motegi1, K Nakamura, T Terakawa, A Oohira, K Minoda, K Kishi, Y Yanagawa, H Hayakawa.   

Abstract

We report a malformed girl with a single chromosome band deletion of 4q26 in peripheral lymphocytes. This patient is the fourth case reported with an interstitial deletion involving 4q26 and has the smallest deletion of those reported. Deletion mapping indicates that psychomotor retardation, coloboma, prominent forehead, epicanthus, broad based nose, and broad, thin upper lip are associated with monosomy 4q26, and that gene(s) associated with Rieger syndrome can be excluded from the 4q26 segment.

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Year:  1988        PMID: 3184142      PMCID: PMC1051542          DOI: 10.1136/jmg.25.9.628

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  5 in total

1.  Interstitial deletion 4q and Rieger syndrome.

Authors:  I Ligutić; L Brecević; I Petković; T Kalogjera; Z Rajić
Journal:  Clin Genet       Date:  1981-11       Impact factor: 4.438

2.  Pericentric inversion and partial monosomy 4q associated with congenital anomalies.

Authors:  F Serville; A Broustet
Journal:  Hum Genet       Date:  1977-11-10       Impact factor: 4.132

3.  Deletions of different segments of the long arm of chromosome 4.

Authors:  J A Mitchell; S Packman; W D Loughman; R M Fineman; E Zackai; S R Patil; B Emanual; J A Bartley; J W Hanson
Journal:  Am J Med Genet       Date:  1981

4.  Inhibitory effect of ethidium bromide on mitotic chromosome condensation and its application to high-resolution chromosome banding.

Authors:  T Ikeuchi
Journal:  Cytogenet Cell Genet       Date:  1984

5.  The human gene map 15 April 1986.

Authors:  V A McKusick
Journal:  Clin Genet       Date:  1986-06       Impact factor: 4.438

  5 in total
  9 in total

1.  Evidence that Rieger syndrome maps to 4q25 or 4q27.

Authors:  C Vaux; L Sheffield; C G Keith; L Voullaire
Journal:  J Med Genet       Date:  1992-04       Impact factor: 6.318

2.  Multiple congenital anomalies including the Rieger eye malformation in a boy with interstitial deletion of (4) (q25-->q27) secondary to a balanced insertion in his normal father: evidence for haplotype insufficiency causing the Rieger malformation.

Authors:  A Schinzel; L Brecevic; F Dutly; A Baumer; F Binkert; R H Largo
Journal:  J Med Genet       Date:  1997-12       Impact factor: 6.318

3.  A new interstitial deletion of 4q (q21.1::q22.1).

Authors:  K Fagan; A Gill
Journal:  J Med Genet       Date:  1989-10       Impact factor: 6.318

Review 4.  Ocular coloboma: a reassessment in the age of molecular neuroscience.

Authors:  C Y Gregory-Evans; M J Williams; S Halford; K Gregory-Evans
Journal:  J Med Genet       Date:  2004-12       Impact factor: 6.318

Review 5.  Toward the complete genomic map and molecular pathology of human chromosome 4.

Authors:  O Riess; B Winkelmann; J T Epplen
Journal:  Hum Genet       Date:  1994-07       Impact factor: 4.132

6.  Potential novel mechanism for Axenfeld-Rieger syndrome: deletion of a distant region containing regulatory elements of PITX2.

Authors:  Bethany A Volkmann; Natalya S Zinkevich; Aki Mustonen; Kala F Schilter; Dmitry V Bosenko; Linda M Reis; Ulrich Broeckel; Brian A Link; Elena V Semina
Journal:  Invest Ophthalmol Vis Sci       Date:  2011-03-18       Impact factor: 4.799

7.  Rieger syndrome locus: a new reciprocal translocation t(4;12)(q25;q15) and a deletion del(4)(q25q27) both break between markers D4S2945 and D4S193.

Authors:  R H Flomen; P A Gorman; R Vatcheva; J Groet; I Barisić; I Ligutić; D Sheer; D Nizetić
Journal:  J Med Genet       Date:  1997-03       Impact factor: 6.318

8.  A new case of an interstitial deletion (4)(q25q27) characterised by molecular cytogenetic techniques and review of the literature.

Authors:  Sandra Anna Becker; Susanne Popp; Klaus Rager; Anna Jauch
Journal:  Eur J Pediatr       Date:  2003-02-19       Impact factor: 3.183

9.  Renal Dysplasia and Progressive Renal Failure in a Newborn with Interstitial Chromosome 4 Deletion 4q25-28.3: A New Phenotype?

Authors:  Cláudia Teles-Silva; Francisca Martins; Sandra Costa; Paulo Soares; Gustavo Rocha; Filipa Flor-de-Lima; Helena Pinto; Carla Ramalho; Renata Oliveira; Otília Brandão; Hercília Guimarães
Journal:  J Pediatr Genet       Date:  2020-01-22
  9 in total

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