Browsing Faculty of Dentistry by Author "Chetty, M"
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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 ... -
Dentinogenesis imperfecta in Osteogenesis imperfecta type XI in South Africa: a genotype–phenotype correlation
Chetty, M; Roberts, T; Shaik, S; Beighton, P (Springer Nature, 2018)BACKGROUND: The maxillofacial and dental manifestations of Osteogenesis imperfecta (OI) have significant implications in terms of management. Although the occurrence of abnormal dentine in some forms of OI is well documented, ... -
Dentinogenesis imperfecta in Osteogenesis imperfecta type XI in South Africa: a genotype–phenotype correlation
Chetty, M (UWC, 2019)BACKGROUND: The maxillofacial and dental manifestations of Osteogenesis imperfecta (OI) have significant implications in terms of management. Although the occurrence of abnormal dentine in some forms of OI is well documented, ... -
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 ...