Literature DB >> 7668296

Minute supernumerary ring chromosome 22 associated with cat eye syndrome: further delineation of the critical region.

A J Mears1, H el-Shanti, J C Murray, H E McDermid, S R Patil.   

Abstract

Cat eye syndrome (CES) is typically associated with a supernumerary bisatellited marker chromosome (inv dup 22pter-22q11.2) resulting in four copies of this region. We describe an individual showing the inheritance of a minute supernumerary double ring chromosome 22, which resulted in expression of all cardinal features of CES. The size of the ring was determined by DNA dosage analysis and FISH analysis for five loci mapping to 22q11.2. The probes to the loci D22S9, D22S43, and ATP6E were present in four copies, whereas D22S57 and D22S181 were present in two copies. This finding further delineates the distal boundary of the critical region of CES, with ATP6E being the most distal duplicated locus identified. The phenotypically normal father and grandfather of the patient each had a small supernumerary ring chromosome and demonstrated three copies for the loci D22S9, D22S43, and ATP6E. Although three copies of this region have been reported in other cases with CES features, it is possible that the presence of four copies leads to greater susceptibility.

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Year:  1995        PMID: 7668296      PMCID: PMC1801256     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  27 in total

1.  RFLPS at the D21S19 locus of human chromosome 21.

Authors:  G D Stewart; R E Tanzi; J F Gusella
Journal:  Nucleic Acids Res       Date:  1985-10-11       Impact factor: 16.971

Review 2.  Unusual cytogenetic mosaicism involving chromosome 14 abnormalities in a child with an MR/MCA syndrome and abnormal pigmentation.

Authors:  E S Cantú; I T Thomas; J L Frias
Journal:  Clin Genet       Date:  1989-09       Impact factor: 4.438

3.  Ring 13 in an adult male with a 13:13 translocation mother.

Authors:  J C de Almeida; J C Llerena; D M Gomes; R R Martins; E T Pereira
Journal:  Ann Genet       Date:  1983

4.  Ring-14 and trisomy 14q in the same child.

Authors:  C Pangalos; V Velissariou; M Ghica; D Liacacos
Journal:  Ann Genet       Date:  1984

5.  Cloned DNA probes regionally mapped to human chromosome 21 and their use in determining the origin of nondisjunction.

Authors:  G D Stewart; P Harris; J Galt; M A Ferguson-Smith
Journal:  Nucleic Acids Res       Date:  1985-06-11       Impact factor: 16.971

Review 6.  Unusual mosaic trisomy 13 through 13/13 translocation and monosomy 13 with a small ring.

Authors:  S M Jalal; J A Martin; T R Benjamin; M K Kukolich; J K Townsend-Parcham
Journal:  Ann Genet       Date:  1990

7.  The gene for human leukemia inhibitory factor (LIF) maps to 22q12.

Authors:  G R Sutherland; E Baker; V J Hyland; D F Callen; J Stahl; N M Gough
Journal:  Leukemia       Date:  1989-01       Impact factor: 11.528

Review 8.  The role of cytologic NOR variants in the etiology of trisomy 21.

Authors:  N B Spinner; D L Eunpu; R D Schmickel; E H Zackai; D McEldrew; G R Bunin; H McDermid; B S Emanuel
Journal:  Am J Hum Genet       Date:  1989-05       Impact factor: 11.025

9.  Characterization of the supernumerary chromosome in cat eye syndrome.

Authors:  H E McDermid; A M Duncan; K R Brasch; J J Holden; E Magenis; R Sheehy; J Burn; N Kardon; B Noel; A Schinzel
Journal:  Science       Date:  1986-05-02       Impact factor: 47.728

10.  A hereditary bisatellite-dicentric supernumerary chromosome in a case of cat-eye syndrome.

Authors:  G Lüleci; G Bağci; M Kivran; E Lüleci; S Bektaş; S Başaran
Journal:  Hereditas       Date:  1989       Impact factor: 3.271

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  16 in total

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2.  Mechanisms and consequences of small supernumerary marker chromosomes: from Barbara McClintock to modern genetic-counseling issues.

Authors:  Erin L Baldwin; Lorraine F May; April N Justice; Christa L Martin; David H Ledbetter
Journal:  Am J Hum Genet       Date:  2008-02       Impact factor: 11.025

3.  Comparative mapping of the human 22q11 chromosomal region and the orthologous region in mice reveals complex changes in gene organization.

Authors:  A Puech; B Saint-Jore; B Funke; D J Gilbert; H Sirotkin; N G Copeland; N A Jenkins; R Kucherlapati; B Morrow; A I Skoultchi
Journal:  Proc Natl Acad Sci U S A       Date:  1997-12-23       Impact factor: 11.205

4.  Update and Review: Supernumerary Marker Chromosomes.

Authors:  S Ungerleider
Journal:  J Genet Couns       Date:  2000-08       Impact factor: 2.537

5.  A common breakpoint on 11q23 in carriers of the constitutional t(11;22) translocation.

Authors:  L Edelmann; E Spiteri; N McCain; R Goldberg; R K Pandita; S Duong; J Fox; D Blumenthal; S R Lalani; L G Shaffer; B E Morrow
Journal:  Am J Hum Genet       Date:  1999-12       Impact factor: 11.025

6.  Transgenic expression of CECR1 adenosine deaminase in mice results in abnormal development of heart and kidney.

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7.  A 600 kb triplication in the cat eye syndrome critical region causes anorectal, renal and preauricular anomalies in a three-generation family.

Authors:  Jeroen Knijnenburg; Yolande van Bever; Lorette O M Hulsman; Chantal A P van Kempen; Galhana M Bolman; Rosa Laura E van Loon; H Berna Beverloo; Laura J C M van Zutven
Journal:  Eur J Hum Genet       Date:  2012-03-07       Impact factor: 4.246

8.  Der(22) syndrome and velo-cardio-facial syndrome/DiGeorge syndrome share a 1.5-Mb region of overlap on chromosome 22q11.

Authors:  B Funke; L Edelmann; N McCain; R K Pandita; J Ferreira; S Merscher; M Zohouri; L Cannizzaro; A Shanske; B E Morrow
Journal:  Am J Hum Genet       Date:  1999-03       Impact factor: 11.025

9.  Coloboma and anorectal malformations: a rare association with important clinical implications.

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10.  Interrupted aortic arch type B in A patient with cat eye syndrome.

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