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Frequency of holoprosencephaly in the International Clearinghouse Birth Defects Surveillance Systems: Searching for population variations
Birth defects research. A Clinical and molecular teratology, 2008-08, Vol.82 (8), p.585-591
Leoncini, Emanuele
Baranello, Giovanni
Orioli, Iêda M.
Annerén, Göran
Bakker, Marian
Bianchi, Fabrizio
Bower, Carol
Canfield, Mark A.
Castilla, Eduardo E.
Cocchi, Guido
Correa, Adolfo
De Vigan, Catherine
Doray, Berenice
Feldkamp, Marcia L.
Gatt, Miriam
Irgens, Lorentz M.
Lowry, R. Brian
Maraschini, Alice
Mc Donnell, Robert
Morgan, Margery
Mutchinick, Osvaldo
Poetzsch, Simone
Riley, Merilyn
Ritvanen, Annukka
Gnansia, Elisabeth Robert
Scarano, Gioacchino
Sipek, Antonin
Tenconi, Romano
Mastroiacovo, Pierpaolo
2008
Details
Autor(en) / Beteiligte
Leoncini, Emanuele
Baranello, Giovanni
Orioli, Iêda M.
Annerén, Göran
Bakker, Marian
Bianchi, Fabrizio
Bower, Carol
Canfield, Mark A.
Castilla, Eduardo E.
Cocchi, Guido
Correa, Adolfo
De Vigan, Catherine
Doray, Berenice
Feldkamp, Marcia L.
Gatt, Miriam
Irgens, Lorentz M.
Lowry, R. Brian
Maraschini, Alice
Mc Donnell, Robert
Morgan, Margery
Mutchinick, Osvaldo
Poetzsch, Simone
Riley, Merilyn
Ritvanen, Annukka
Gnansia, Elisabeth Robert
Scarano, Gioacchino
Sipek, Antonin
Tenconi, Romano
Mastroiacovo, Pierpaolo
Titel
Frequency of holoprosencephaly in the International Clearinghouse Birth Defects Surveillance Systems: Searching for population variations
Ist Teil von
Birth defects research. A Clinical and molecular teratology, 2008-08, Vol.82 (8), p.585-591
Ort / Verlag
Hoboken: Wiley Subscription Services, Inc., A Wiley Company
Erscheinungsjahr
2008
Link zum Volltext
Quelle
MEDLINE
Beschreibungen/Notizen
BACKGROUND: Holoprosencephaly (HPE) is a developmental field defect of the brain that results in incomplete separation of the cerebral hemispheres that includes less severe phenotypes, such as arhinencephaly and single median maxillary central incisor. Information on the epidemiology of HPE is limited, both because few population‐based studies have been reported, and because small studies must observe a greater number of years in order to accumulate sufficient numbers of births for a reliable estimate. METHODS: We collected data from 2000 through 2004 from 24 of the 46 Birth Defects Registry Members of the International Clearinghouse for Birth Defects Surveillance and Research. This study is based on more than 7 million births in various areas from North and South America, Europe, and Australia. RESULTS: A total of 963 HPE cases were registered, yielding an overall prevalence of 1.31 per 10,000 births. Because the estimate was heterogeneous, possible causes of variations among populations were analyzed: random variation, under‐reporting and over‐reporting bias, variation in proportion of termination of pregnancies among all registered cases and real differences among populations. CONCLUSIONS: The data do not suggest large differences in total prevalence of HPE among the studied populations that would be useful to generate etiological hypotheses. Birth Defects Research (Part A), 2008. © 2008 Wiley‐Liss, Inc.
Sprache
Englisch
Identifikatoren
ISSN: 1542-0752, 1542-0760
eISSN: 1542-0760
DOI: 10.1002/bdra.20479
Titel-ID: cdi_swepub_primary_oai_DiVA_org_uu_17380
Format
–
Schlagworte
Americas
,
Australia
,
brain malformations
,
Congenital Abnormalities - epidemiology
,
epidemiology
,
Europe
,
Female
,
holoprosencephaly
,
Holoprosencephaly - epidemiology
,
Humans
,
ICBDSR
,
International Cooperation
,
Live Birth - epidemiology
,
MEDICIN
,
MEDICINE
,
Population Surveillance - methods
,
Pregnancy
,
Prevalence
,
Registries
,
Stillbirth - epidemiology
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