Browsing Centre for Environmental and Preventive Medicine (CEPM) by Author "Neville, AJ"
Now showing items 1-7 of 7
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Epidemiology of septo-optic dysplasia with focus on prevalence and maternal age - A EUROCAT study.
Garne, E; Rissmann, A; Addor, M-C; Barisic, I; Bergman, J; Braz, P; Cavero-Carbonell, C; Draper, ES; Gatt, M; Haeusler, M (2018-09)Septo-optic nerve dysplasia is a rare congenital anomaly with optic nerve hypoplasia, pituitary hormone deficiencies and midline developmental defects of the brain. The clinical findings are visual impairment, hypopituitarism ... -
Estimating the birth prevalence and pregnancy outcomes of congenital malformations worldwide.
Moorthie, S; Blencowe, H; Darlison, MW; Lawn, J; Morris, JK; Modell, B; Congenital Disorders Expert Group; Bittles, AH; Blencowe, H; Christianson, A (2018-10)Congenital anomaly registries have two main surveillance aims: firstly to define baseline epidemiology of important congenital anomalies to facilitate programme, policy and resource planning, and secondly to identify ... -
EUROmediCAT signal detection: an evaluation of selected congenital anomaly-medication associations.
Given, JE; Loane, M; Luteijn, JM; Morris, JK; de Jong van den Berg, LTW; Garne, E; Addor, M-C; Barisic, I; de Walle, H; Gatt, M (2016-10)AIMS: To evaluate congenital anomaly (CA)-medication exposure associations produced by the new EUROmediCAT signal detection system and determine which require further investigation. METHODS: Data from 15 EUROCAT registries ... -
Methods to estimate access to care and the effect of interventions on the outcomes of congenital disorders
Christianson, A; Cousens, S; Darlison, M; Gibbons, S; Hamamy, H; Khoshnood, B; Howson, CP; Lawn, JE; Mastroiacovo, P; Modell, B (2018-10-01)© 2018, The Author(s). In the absence of intervention, early-onset congenital disorders lead to pregnancy loss, early death, or disability. Currently, lack of epidemiological data from many settings limits the understanding ... -
Prevalence of microcephaly in Europe: population based study
Morris, JK; Rankin, J; Garne, E; Loane, M; Greenlees, R; Addor, M-C; Arriola, L; Barisic, I; Bergman, JEH; Csaky-Szunyogh, M (2016-09-13) -
Rare single gene disorders: estimating baseline prevalence and outcomes worldwide
Blencowe, H; Moorthie, S; Petrou, M; Hamamy, H; Povey, S; Bittles, A; Gibbons, S; Darlison, M; Modell, B; Bittles, AH (2018-10-01)© 2018, The Author(s). As child mortality rates overall are decreasing, non-communicable conditions, such as genetic disorders, constitute an increasing proportion of child mortality, morbidity and disability. To date, ... -
Trends in congenital anomalies in Europe from 1980 to 2012.
Morris, JK; Springett, AL; Greenlees, R; Loane, M; Addor, M-C; Arriola, L; Barisic, I; Bergman, JEH; Csaky-Szunyogh, M; Dias, C (2018)BACKGROUND: Surveillance of congenital anomalies is important to identify potential teratogens. METHODS: This study analysed the prevalence of 61 congenital anomaly subgroups (excluding chromosomal) in 25 population-based ...