ABSTRACT
Elsinoe takoropuku sp. nov. is described from Pittosporum tenuifolium Sol. ex Gaertn. (Pittosporaceae). This species causes swelling to develop on the twigs of the host species. The species initially was thought to be a recent introduction to New Zealand but, based on the host association and the geographic range of the fungus in New Zealand, it is considered to be a newly described native species.
Subject(s)
Ascomycota/isolation & purification , Plant Diseases/microbiology , Rosales , Ascomycota/ultrastructure , New Zealand , Plant Stems/microbiologyABSTRACT
This is the first population based study to estimate the birth prevalence of DNA proven Prader-Willi syndrome. Thirty infants were reported to the Australian Paediatric Surveillance Unit between 1998 and 2000, a prevalence of 4 per 100,000 live births or approximately 1/25,000 live births per annum.
Subject(s)
Prader-Willi Syndrome/epidemiology , Adolescent , Australia/epidemiology , Child , Child, Preschool , DNA/analysis , Female , Humans , Infant , Infant, Newborn , Male , Prader-Willi Syndrome/genetics , PrevalenceABSTRACT
The Australian Paediatric Surveillance Unit (APSU), through active surveillance, collects information on the epidemiology of rare or uncommon childhood conditions. This research resource allows paediatricians to collaborate at State, national and international levels. The APSU sends a monthly report card to all (currently 971) paediatricians in Australia, who in turn indicate whether or not they have seen a patient in the last month with any of the conditions listed (98% response rate in 1999). Study investigators, notified by the APSU of positive case reports, obtain demographic and clinical data on the patient from the reporting doctor by postal questionnaire (90% response rate in 1999). Since 1993, the APSU has monitored 27 conditions, including conditions that are vaccine-preventable, otherwise infectious, genetic, congenital and non-communicable. Information collected is disseminated to paediatricians and other health professionals via an annual report, newsletters and publications and is made available to the International Network of Paediatric Surveillance Units. Information provided by the APSU has raised awareness among paediatricians of rare and uncommon childhood conditions, and has been used by health authorities for planning of prevention and intervention strategies and allocation of health resources.
Subject(s)
Child Welfare/statistics & numerical data , Pediatrics/statistics & numerical data , Population Surveillance , Australia/epidemiology , Child , Child, Preschool , Communicable Diseases/epidemiology , Congenital Abnormalities/epidemiology , Humans , Incidence , Infant , Infant, Newborn , Infant, Newborn, Diseases/epidemiology , Information Services , Organizational Objectives , Public Health Administration , Surveys and QuestionnairesABSTRACT
This study explored the notion that the extent to which language-impaired children can become bilingual depends on the type of language impairment. Single-case studies were conducted on two 7-year-old bilingual children, who had both been exposed to English and Afrikaans consistently and regularly from an early age. The subjects presented with specific language impairment (SLI) and semantic-pragmatic disorder (SPD), respectively. They were assessed on a battery of cognitive and linguistic tests in both their languages. Results indicate that the SLI subject, who presented with a deficit in successive processing on the Cognitive Assessment System, had difficulty in acquiring the surface features of both languages. She developed much better proficiency in English than in Afrikaans, despite substantial exposure to the latter. The SPD subject, whose cognitive profile was characterised by planning and attention deficits, but a strength in successive processing, presented with equal proficiency in both languages. The theoretical and clinical implications of this research are discussed.
Subject(s)
Cognition Disorders/diagnosis , Language Disorders/diagnosis , Linguistics , Multilingualism , Child , Cognition Disorders/therapy , Female , Humans , Language Disorders/therapy , Male , SemanticsABSTRACT
BACKGROUND: The International Network of Paediatric Surveillance Units (INoPSU) was established in 1998 and met formally for the first time in Ottawa, Ontario in June 2000. OBJECTIVES: To document the methodology and activities of existing national paediatric surveillance units; the formation of INoPSU; the diseases studied by INoPSU members; and the impact of such studies on education, public health and paediatric practice. METHODS: Directors of paediatric surveillance units in Australia, Britain, Canada, Germany, the Netherlands, Latvia, Malaysia, Papua New Guinea, New Zealand and Switzerland were asked to provide information on each unit's affiliations, funding and staffing; the method of case ascertainment, the mailing list and response rates; and diseases studied. Original articles that reported data derived from units were identified by a search of an electronic database (MEDLINE), and additional information was obtained from units' annual reports. RESULTS: Worldwide, 10 units (established from 1986 to 1997), use active national surveillance of more than 8500 clinicians each month to identify cases of rare or uncommon diseases in a childhood population (younger than 15 years of age) of over 47 million (monthly response rate 73% to 98%). By January 1999, units had initiated 147 studies on 103 different conditions, and 63 studies were completed. CONCLUSION: INoPSU enhances collaboration among units from four continents, providing a unique opportunity for simultaneous cross-sectional studies of rare diseases in populations with diverse geographical and ethnic characteristics. It facilitates the sharing of ideas regarding current methodology, ethics, the most appropriate means of evaluating units and their potential application.
