Browsing Research Publications by Author "Roberts, T"
Now showing items 1-6 of 6
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Dental needs of intellectually disabled children attending six special educational facilities in Cape Town
(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
(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, ... -
Oral medicine case book 55: ondontogenic myxoma
(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
(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
(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
(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 ...
