| Literature DB >> 27614115 |
Tiffany Busa1, Nicoleta Panait2, Kathia Chaumoitre3, Nicole Philip4, Chantal Missirian5.
Abstract
Terminal 7q deletion is rarely reported in the literature. Holoprosencephaly and sacral dysgenesis are found in association with this deletion, due to haploinsufficiency of SHH and HLBX9 genes respectively. We report on a 2-year-old boy with 7q35-36.3 deletion encompassing SHH identified by oligonucleotide array comparative genomic hybridization. In addition to other frequent features, the patient presented with esophageal atresia and tracheoeosophageal fistula diagnosed at birth. This case, together with two others previously described, one presenting with esophageal atresia, the other with congenital esophageal stenosis, confirms the possible association between congenital esophageal malformations and 7q terminal deletion including SHH.Entities:
Keywords: 7q terminal deletion; Oesophageal atresia; SHH gene; Tracheoesophageal fistula
Mesh:
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Year: 2016 PMID: 27614115 DOI: 10.1016/j.ejmg.2016.09.001
Source DB: PubMed Journal: Eur J Med Genet ISSN: 1769-7212 Impact factor: 2.708