Article Text

other Versions

PDF
Phenotype and genotype in 17 patients with Goltz-Gorlin Syndrome
  1. S M Maas
  1. Department of Paediatric Genetics, Academic Medical Centre, Amsterdam, Netherlands
    1. P M Lombardi
    1. Department of Clinical Genetics, Academic Medical Centre, Amsterdam, Netherlands
      1. A J Van Essen
      1. Department of Genetics, UMCG, University of Groningen, Groningen, Netherlands
        1. E L Wakeling
        1. Department of Clinical Genetics, Kennedy-Galton Centre, London, United Kingdom
          1. B Castle
          1. Wessex Clinical Genetics Service, Southampton, United Kingdom
            1. I K Temple
            1. Academic Unit of Genetic Medicine, Southampton, United Kingdom
              1. V K A Kumar
              1. Department of Clinical Genetics, Great Ormond Street Hospital, UCL, London, United Kingdom
                1. K Writzl
                1. Institute of Medical Genetics, Ljubljana, Slovenia
                  1. R C M Hennekam (r.hennekam{at}ich.ucl.ac.uk)
                  1. Clinical and Molecular Genetics Unit, Institute of Child Health, UCL, London, United Kingdom

                    Abstract

                    Goltz-Gorlin syndrome or focal dermal hypoplasia is a highly variable, X-linked dominant syndrome with abnormalities of ectodermal and mesodermal origin. In 2007 mutations in the PORCN gene were found to be causative in Goltz-Gorlin syndrome.

                    Here we report on a series of 17 Goltz-Gorlin patients, and describe their phenotype and genotype. In 14 patients, 13 females and one male, a PORCN mutation was found. Mutations included nonsense (n=5), frameshift (n=2), aberrant splicing (n=2), and missense (n=5) mutations. No genotype-phenotype correlation could be found. All patients with the classical features of the syndrome had a detectable mutation. In three females with atypical signs no mutation could be found. The male patient had classical features and showed a mosaicism for a PORCN nonsense mutation in fibroblasts. Two affected sisters had a mutation not detectable in their parents, supporting germline mosaicism. Their father had undergone radiation for testicular cancer in the past. Two classically affected females had three severely affected female fetuses which all had midline thoracic and abdominal wall defects, resembling the pentalogy of Cantrell and the limb-body wall complex. Thoracic and abdominal wall defects were also present in two surviving patients. Possibly, PORCN mutations can cause pentalogy of Cantrell and limb-body wall complexes as well, and particularly in cases with limb defects it seems useful to search for these.

                    We conclude that PORCN mutations can be found in all classically affected cases with Goltz-Gorlin syndrome, including males. Somatic and germline mosaicism occur. There is no evident genotype-phenotype correlation.

                    Statistics from Altmetric.com

                    Request permissions

                    If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.