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Microdeletions including YWHAE in the Miller-Dieker syndrome region on chromosome 17p13.3 result in facial dysmorphisms, growth restriction, and cognitive impairment
  1. S C Sreenath Nagamani
  1. Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, United States
    1. F Zhang
    1. Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, United States
      1. O A Shchelochkov
      1. Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, United States
        1. W Bi
        1. Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, United States
          1. Z Ou
          1. Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, United States
            1. F Scaglia
            1. Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, United States
              1. F J Probst
              1. Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, United States
                1. M Shinawi
                1. Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, United States
                  1. C Eng
                  1. Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, United States
                    1. J V Hunter
                    1. Department of Radiology, Baylor College of Medicine, Houston, TX, United States
                      1. S Sparagana
                      1. Department of Neurology, Texas Scottish Rite Hospital for Children, Dallas, TX, United States
                        1. E Lagoe
                        1. Department of Pediatrics, University of Rochester Medical Center, Rochester, NY, United States
                          1. Chin -to- Fong
                          1. Department of Pediatrics, University of Rochester Medical Center, Rochester, NY, United States
                            1. M Pearson
                            1. Neonatology Associates, Ltd., Phoenix, AZ, United States
                              1. M Doco-Fenzy
                              1. Service de Génétique, HMB, CHRU, UFR de médecine, EA3801, Reims, France
                                1. E Landais
                                1. Service de Génétique, HMB, CHRU, UFR de médecine, EA3801, Reims, France
                                  1. M Mozelle
                                  1. Service de Génétique, HMB, CHRU, UFR de médecine, EA3801, Reims, France
                                    1. A C Chinault
                                    1. Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, United States
                                      1. A Patel
                                      1. Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, United States
                                        1. C A Bacino
                                        1. Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, United States
                                          1. T Sahoo
                                          1. Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, United States
                                            1. S-H Kang
                                            1. Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, United States
                                              1. S W Cheung
                                              1. Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, United States
                                                1. J R Lupski
                                                1. Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, United States
                                                  1. P Stankiewicz (pawels{at}bcm.edu)
                                                  1. Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, United States

                                                    Abstract

                                                    Deletions in the 17p13.3 region are associated with abnormal neuronal migration. Point mutations or deletion copy number variants of the PAFAH1B1 gene in this genomic region cause lissencephaly whereas extended deletions involving both PAFAH1B1 and YWHAE result in Miller-Dieker syndrome characterized by facial dysmorphisms and a more severe grade of lissencephaly. The phenotypic consequences of YWHAE deletion without deletion of PAFAH1B1 have not been studied systematically. We performed a detailed clinical and molecular characterization of five patients with deletions involving YWHAE but not PAFAH1B1, two with deletion including PAFAH1B1 but not YWHAE and one with deletion of YWHAE and mosaic for deletion of PAFAH1B1. Three deletions were terminal whereas five were interstitial. Patients with deletions including YWHAE but not PAFAH1B1 presented with significant growth restriction, cognitive impairment, shared craniofacial features, and variable structural abnormalities of the brain. Growth restriction was not observed in one patient with deletion of YWHAE and TUSC5, implying that other genes in the region may have a role in regulation of growth with CRK being the most likely candidate. Using array based comparative genomic hybridization and long range PCR, we have delineated the breakpoints of these non-recurrent deletions and show that the interstitial genomic rearrangements are likely generated by diverse mechanisms, including the recently described Fork Stalling and Template Switching (FoSTeS)/ Microhomology Mediated Break Induced Replication (MMBIR).

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