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 ...
  • Oral medicine case book 55: ondontogenic myxoma 

    Holmes, Haly; Mulder, Sune; Dreyer, Wynand P.; Fakir, E.; Roberts, T.; Wainright, H. (South African Dental Association (SADA), 2013)
    A 20-year old female was referred from her local community health clinic to the Oral Medicine Clinic at Groote Schuur Hospital for a swelling that started out as a small and painless lesion. She had attended the local ...
  • 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 ...