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Neuropediatrics 2004; 35(1): 10-19
DOI: 10.1055/s-2003-43552
Original Article

Georg Thieme Verlag Stuttgart · New York

Coats' Plus: A Progressive Familial Syndrome of Bilateral Coats' Disease, Characteristic Cerebral Calcification, Leukoencephalopathy, Slow Pre- and Post-Natal Linear Growth and Defects of Bone Marrow and Integument

Y. J. Crow 1 , 2 , J. McMenamin 3 , C. A. Haenggeli 4 , D. M. Hadley 5 , S. Tirupathi 6 , E. P. Treacy 6 , S. M. Zuberi 7 , B. H. Browne 8 , J. L. Tolmie 9 , J. B. P. Stephenson 7
  • 1Molecular Medicine Unit, University of Leeds, St James's University Hospital, Leeds, UK
  • 2Department of Clinical Genetics, St James's University Hospital, Leeds, UK
  • 3Our Lady's Hospital for Sick Children, Crumlin, Dublin, Eire
  • 4Department of Child Neurology, Hôpital des Enfants, Geneva, Switzerland
  • 5Neuroradiology Department, Institute of Neurological Sciences, Southern General Hospital, Glasgow, UK
  • 6Department of Paediatrics, The Children's University Hospital, Dublin, Eire
  • 7Fraser of Allander Neurosciences Unit, Royal Hospital for Sick Children, Glasgow, UK
  • 8Eye Department, Royal Infirmary, Glasgow, UK
  • 9Department of Medical Genetics, Royal Hospital for Sick Children, Glasgow, UK