Literature DB >> 11484198

Distal deletion, del(2)(q33.3q33.3), in a patient with severe growth deficiency and minor anomalies.

M Riegel1, E Morava, M Czakó, G Kosztolányi, A Schinzel.   

Abstract

We report on an 18-month-old boy with a 2q33.3 deletion. The clinical findings observed in the propositus included minor anomalies of face and distal limbs, intrauterine and postnatal growth retardation, microcephaly and, so far, moderate developmental delay. Conventional GTG banded chromosome analysis indicated a small deletion in distal 2q. Subsequent analysis by fluorescent in situ hybridization (FISH) using different probes allowed us to narrow down the deletion to most or all of segment 2q33.3. This case shows the importance of the application of different YAC probes for a precise determination of breakpoints in small interstitial deletions. Copyright 2001 Wiley-Liss, Inc.

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Year:  2001        PMID: 11484198     DOI: 10.1002/ajmg.1455

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  2 in total

1.  Autistic and dysmorphic features associated with a submicroscopic 2q33.3-q34 interstitial deletion detected by array comparative genomic hybridization.

Authors:  Duane T Brandau; Molly Lund; Linda D Cooley; Warren G Sanger; Merlin G Butler
Journal:  Am J Med Genet A       Date:  2008-02-15       Impact factor: 2.802

Review 2.  A multiple translocation event in a patient with hexadactyly, facial dysmorphism, mental retardation and behaviour disorder characterised comprehensively by molecular cytogenetics. Case report and review of the literature.

Authors:  Jörg Seidel; Anita Heller; Gabriele Senger; Heike Starke; Ilse Chudoba; Christina Kelbova; Holger Tönnies; Heidemarie Neitzel; Claudia Haase; Volkmar Beensen; Felix Zintl; Uwe Claussen; Thomas Liehr
Journal:  Eur J Pediatr       Date:  2003-06-19       Impact factor: 3.183

  2 in total

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