Now showing items 1-6 of 6

  • Dental needs of intellectually disabled children attending six special educational facilities in Cape Town 

    Roberts, T.; Chetty, M.; Kimmie-Dhansay, F.; Fieggen, K.; Stephen, Lawrence X.G.S. (Health & Medical Publishing Group, 2016)
    OBJECTIVE. To assess the dental needs of a group of children with intellectual disability (ID) attending six special educational facilities in Cape Town, South Africa. METHODS. This was a cross-sectional study based on ...
  • Osteogenesis imperfecta type III in South Africa: Psychosocial challenges 

    Stephen, Lawrence X.G.S.; Roberts, Tina; van Hayden, E.; Chetty, M. (Health and Medical Publishing Group, 2016)
    Individuals with osteogenesis imperfecta type III (OI III) are severely physically disabled due to frequent fracturing. Their disability poses numerous barriers that challenge their social development. Despite these ...
  • Osteoporosis-pseudoglioma syndrome in South Africa 

    Chetty, M.; Stephen, Lawrence X.G.S.; Roberts, T. (Health and Medical Publishing Group, 2016)
    The osteoporosis-pseudoglioma syndrome (MIM 259770) is a rare autosomal recessive disorder in which bone fragility and frequent fractures are associated with serious ocular changes. The skeletal manifestations resemble ...
  • Osteoporosis-pseudoglioma syndrome in South Africa 

    Chetty, M.; Stephen, Lawrence X.G.S.; Roberts, T. (Health & Medical Publishing Group, 2016)
    The osteoporosis-pseudoglioma syndrome (MIM 259770) is a rare autosomal recessive disorder in which bone fragility and frequent fractures are associated with serious ocular changes. The skeletal manifestations resemble ...
  • Pyle metaphyseal dysplasia in an African child: Case report and review of the literature 

    Wonkam, A.; Makubalo, N.; Roberts, T.; Chetty, M. (Health & Medical Publishing Group, 2016)
    Pyle disease (OMIM 265900), also known as metaphyseal dysplasia, is a rare autosomal recessive disorder with no known gene mutation. We report a case of Pyle disease in a 7-year-old African boy of mixed ancestry who ...
  • Pyle metaphyseal dysplasia in an African child: case report and review of the literature 

    Wonkam, A.; Makubalo, N.; Roberts, T.; Chetty, M. (Health and Medical Publishing Group, 2016-06)
    Pyle disease (OMIM 265900), also known as metaphyseal dysplasia, is a rare autosomal recessive disorder with no known gene mutation. We report a case of Pyle disease in a 7-year-old African boy of mixed ancestry who ...