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1.
Public Health Nutr ; 4(3): 757-64, 2001 Jun.
Article in English | MEDLINE | ID: mdl-11415482

ABSTRACT

OBJECTIVE: To identify the season with the highest prevalence of underweight among young children and to examine geographical variation in seasonality of underweight. DESIGN: This analysis is based on monthly data from a clinic-based growth monitoring programme that forms part of the National Health Information System. A regression-based technique is used to identify seasonal patterns in both underweight prevalence and attendance nationally and in 60 different districts. SETTING: The analysis covers the period 1988-1995 and is based in Zimbabwe. SUBJECTS: The analysis is based on weight-for-age measurements of Zimbabwean children less than 5 years old, who attended health centres as part of a growth monitoring programme. RESULTS: Nationally, a small but significant increase in levels of underweight takes place during January-March. Participation in growth monitoring also varies seasonally and could account for the increase observed. No evidence of seasonal variation in underweight prevalence is found in the majority of districts studied, although 11 of the districts showed a similar pattern to the national data set. This peak in the incidence of poor nutritional status also coincides with the period of food scarcity before harvest, which is also associated with higher prevalence of diarrhoea and malaria. No differences in seasonality of under-nutrition were found between districts with predominantly subsistence agriculture and those with more commercial forms of agriculture. CONCLUSIONS: Seasonal variation in child weight-for-age exists in some parts of Zimbabwe, but its effects on cross-sectional prevalence studies are likely to be small. There are no readily discernible differences between areas that show evidence of seasonality in levels of underweight and those that do not.


Subject(s)
Body Weight , Child Nutrition Disorders/epidemiology , Seasons , Age Factors , Child, Preschool , Cross-Sectional Studies , Female , Humans , Infant , Infant, Newborn , Male , Nutrition Surveys , Prevalence , Zimbabwe/epidemiology
2.
J Laryngol Otol ; 97(3): 251-9, 1983 Mar.
Article in English | MEDLINE | ID: mdl-6833850

ABSTRACT

Salivary gland type adenomas of the nasal septum are rare tumors in adults and even rarer in children. There has been no previous report of such a tumor in a neonate. We have described a tumor of the nasal septum whose light and electron microscopic appearances are consistent with an origin from minor salivary gland or nasal mucous glands. Ultrastructural findings presented do not suggest an origin from the embryonic organ of Jacobson (vomeronasal organ). The biological behaviour of this tumor in the neonate is unknown. A study of similar cases will be necessary to elucidate the incidence and natural history of intranasal adenomas in the neonate.


Subject(s)
Adenoma/congenital , Nose Neoplasms/congenital , Adenoma/ultrastructure , Female , Humans , Infant, Newborn , Microscopy, Electron , Nasal Septum , Nose Neoplasms/ultrastructure
4.
Lancet ; 1(7900): 195-7, 1975 Jan 25.
Article in English | MEDLINE | ID: mdl-47422

ABSTRACT

A large inbred family is described in which there were seven cases of Hodgkin's disease, three of lymphosarcoma, two of thymoma, two of common variable immunodeficiency, and single cases of retinoblastoma, neuroblastoma, and rhabdomyosarcoma. There have been no other lymphoma cases in the community during the past decade. Further study of this family may help to define the genetic basis for development of Hodgkin's disease and other disorders.


Subject(s)
Hodgkin Disease/genetics , Immunologic Deficiency Syndromes/genetics , Adult , Autopsy , Biopsy , Child , Child, Preschool , Consanguinity , Female , Hodgkin Disease/pathology , Hodgkin Disease/transmission , Humans , Inbreeding , Infant , Lymphoma, Non-Hodgkin/genetics , Male , Middle Aged , Neoplasms/genetics , Neuroblastoma/genetics , Newfoundland and Labrador , Pedigree , Retinoblastoma/genetics , Rhabdomyosarcoma/genetics , Sarcoma/genetics , Thymoma/genetics
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