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Genomic imbalances associated with müllerian aplasia
  1. Carola Cheroki (gene_adict{at}yahoo.com)
  1. Institute of Biosciences - University of São Paulo, Brazil
    1. Ana C V Krepischi-Santos (krepisch{at}ib.usp.br)
    1. Institute of Biosciences - University of São Paulo, Brazil
      1. Károly Szuhai (k.szuhai{at}lumc.nl)
      1. Leiden University Medical Center, Netherlands
        1. Volker Brenner (douglas.hurd{at}ogt.co.uk)
        1. Oxford Gene Technology, United Kingdom
          1. Chong AE Kim (chong{at}icr.hcnet.usp.br)
          1. Genetics Unit, Department of Pediatrics, Children Institute, University of São Paulo, Brazil
            1. Paulo A Otto (otto{at}ib.usp.br)
            1. Institute of Biosciences - University of São Paulo, Brazil
              1. Carla Rosenberg (carlarosenberg{at}uol.com.br)
              1. Institute of Biosciences - University of São Paulo, Brazil

                Abstract

                Background: Aplasia of the müllerian ducts leads to absence of the uterine corpus, uterine cervix, and upper (superior) vagina. Patients with müllerian aplasia (MA) often exhibit additional clinical features such as renal, vertebral and cardiac defects. A number of different syndromes have been associated to MA, and in most cases its etiology remains poorly understood. Objective and methods: Fourteen syndromic patients with MA and 46,XX G-banded karyotype were screened for DNA copy number changes by ~1 Mb whole genome BAC array-CGH. The detected alterations were validated by an independent method and further mapped by high-resolution oligo-arrays. Results: Submicroscopic genomic imbalances affecting the 1q21.1, 17q12, 22q11.21, and Xq21.31 chromosome regions were detected in four probands. Presence of the alterations in the normal mother of one patient suggests incomplete penetrance and/or variable expressivity. Conclusion: 4 of the 14 patients (29%) were found to have cryptic genomic alterations. The imbalances on 22q11.21 support recent findings by us and others that alterations in this chromosome region may result in impairment of müllerian ducts development. The remaining imbalances indicate involvement of previously unknown chromosome regions in MA, and point specifically to LHX1 and KLHL4 as candidate genes.

                • array-CGH
                • genomic imbalances
                • müllerian aplasia
                • uterus agenesis

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