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19q13.11 deletion syndrome: a novel clinically recognisable genetic condition identified by array comparative genomic hybridisation
  1. V Malan1,2,
  2. O Raoul1,2,
  3. H V Firth3,
  4. G Royer1,
  5. C Turleau1,2,
  6. A Bernheim4,
  7. L Willatt3,
  8. A Munnich1,
  9. M Vekemans1,
  10. S Lyonnet1,2,
  11. V Cormier-Daire1,2,
  12. L Colleaux1,2
  1. 1
    INSERM U781 et Département de Génétique, Hôpital Necker-Enfants Malades, Paris, France
  2. 2
    Université Paris Descartes, Paris, France
  3. 3
    Department of Medical Genetics, Box 134 Addenbrooke’s Hospital, Cambridge, UK
  4. 4
    CNRS FRE2939 Institut Gustave Roussy, Villejuif, France and Université Paris Sud, Orsay, France
  1. Correspondence to Dr V Malan, Service de Cytogénétique et d’Embryologie, Hôpital Necker-Enfants Malades, 149, rue de Sèvres, 75743 Paris Cedex 15, France; Valerie.malan{at}nck.aphp.fr

Abstract

Background: Deletions of chromosome 19 have rarely been reported, with the exception of some patients with deletion 19q13.2 and Blackfan–Diamond syndrome due to haploinsufficiency of the RPS19 gene. Such a paucity of patients might be due to the difficulty in detecting a small rearrangement on this chromosome that lacks a distinct banding pattern. Array comparative genomic hybridisation (CGH) has become a powerful tool for the detection of microdeletions and microduplications at high resolution in patients with syndromic mental retardation.

Methods and results: Using array CGH, this study identified three interstitial overlapping 19q13.11 deletions, defining a minimal critical region of 2.87 Mb, associated with a clinically recognisable syndrome. The three patients share several major features including: pre- and postnatal growth retardation with slender habitus, severe postnatal feeding difficulties, microcephaly, hypospadias, signs of ectodermal dysplasia, and cutis aplasia over the posterior occiput. Interestingly, these clinical features have also been described in a previously reported patient with a 19q12q13.1 deletion. No recurrent breakpoints were identified in our patients, suggesting that no-allelic homologous recombination mechanism is not involved in these rearrangements.

Conclusions: Based on these results, the authors suggest that this chromosomal abnormality may represent a novel clinically recognisable microdeletion syndrome caused by haploinsufficiency of dosage sensitive genes in the 19q13.11 region.

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Footnotes

  • Competing interests None declared.

  • Patient consent Obtained.

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