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Your search keyword '"O'Mahony, Mary T."' showing total 8 results
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8 results on '"O'Mahony, Mary T."'

2. Amniotic band syndrome and limb body wall complex in Europe 1980–2019

Author

Bergman, Jorieke E. H., primary, Barišić, Ingeborg, additional, Addor, Marie‐Claude, additional, Braz, Paula, additional, Cavero‐Carbonell, Clara, additional, Draper, Elizabeth S., additional, Echevarría‐González‐de‐Garibay, Luis J., additional, Gatt, Miriam, additional, Haeusler, Martin, additional, Khoshnood, Babak, additional, Klungsøyr, Kari, additional, Kurinczuk, Jennifer J., additional, Latos‐Bielenska, Anna, additional, Luyt, Karen, additional, Martin, Danielle, additional, Mullaney, Carmel, additional, Nelen, Vera, additional, Neville, Amanda J., additional, O'Mahony, Mary T., additional, Perthus, Isabelle, additional, Pierini, Anna, additional, Randrianaivo, Hanitra, additional, Rankin, Judith, additional, Rissmann, Anke, additional, Rouget, Florence, additional, Sayers, Gerardine, additional, Schaub, Bruno, additional, Stevens, Sarah, additional, Tucker, David, additional, Verellen‐Dumoulin, Christine, additional, Wiesel, Awi, additional, Gerkes, Erica H., additional, Perraud, Annie, additional, Loane, Maria A., additional, Wellesley, Diana, additional, and de Walle, Hermien E. K., additional

Published
2022
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4. Prevalence of vascular disruption anomalies and association with young maternal age: A EUROCAT study to compare the United Kingdom with other European countries

Author

Morris, Joan K., primary, Wellesley, Diana, additional, Limb, Elizabeth, additional, Bergman, Jorieke E. H., additional, Kinsner‐Ovaskainen, Agnieszka, additional, Addor, Marie Claude, additional, Broughan, Jennifer M., additional, Cavero‐Carbonell, Clara, additional, Dias, Carlos M., additional, Echevarría‐González‐de‐Garibay, Luis‐Javier, additional, Gatt, Miriam, additional, Haeusler, Martin, additional, Barisic, Ingeborg, additional, Klungsoyr, Kari, additional, Lelong, Nathalie, additional, Materna‐Kiryluk, Anna, additional, Neville, Amanda, additional, Nelen, Vera, additional, O'Mahony, Mary T., additional, Perthus, Isabelle, additional, Pierini, Anna, additional, Rankin, Judith, additional, Rissmann, Anke, additional, Rouget, Florence, additional, Sayers, Geraldine, additional, Stevens, Sarah, additional, Tucker, David, additional, and Garne, Ester, additional

Published
2022
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5. Epidemiology of aplasia cutis congenita: A population‐based study in Europe

Author

Coi, Alessio, primary, Barisic, Ingeborg, additional, Garne, Ester, additional, Pierini, Anna, additional, Addor, Marie‐Claude, additional, Aizpurua Atxega, Amaia, additional, Ballardini, Elisa, additional, Braz, Paula, additional, Broughan, Jennifer M., additional, Cavero‐Carbonell, Clara, additional, de Walle, Hermien E. K., additional, Draper, Elizabeth S., additional, Gatt, Miriam, additional, Häusler, Martin, additional, Kinsner‐Ovaskainen, Agnieszka, additional, Kurinczuk, Jennifer J., additional, Lelong, Nathalie, additional, Luyt, Karen, additional, Mezzasalma, Lorena, additional, Mullaney, Carmel, additional, Nelen, Vera, additional, Odak, Ljubica, additional, O'Mahony, Mary T., additional, Perthus, Isabelle, additional, Randrianaivo, Hanitra, additional, Rankin, Judith, additional, Rissmann, Anke, additional, Rouget, Florence, additional, Schaub, Bruno, additional, Tucker, David, additional, Wellesley, Diana, additional, Wiśniewska, Katarzyna, additional, Yevtushok, Lyubov, additional, and Santoro, Michele, additional

Published
2022
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7. Amniotic band syndrome and limb body wall complex in Europe 1980–2019.

Author

Bergman, Jorieke E. H., Barišić, Ingeborg, Addor, Marie‐Claude, Braz, Paula, Cavero‐Carbonell, Clara, Draper, Elizabeth S., Echevarría‐González‐de‐Garibay, Luis J., Gatt, Miriam, Haeusler, Martin, Khoshnood, Babak, Klungsøyr, Kari, Kurinczuk, Jennifer J., Latos‐Bielenska, Anna, Luyt, Karen, Martin, Danielle, Mullaney, Carmel, Nelen, Vera, Neville, Amanda J., O'Mahony, Mary T., and Perthus, Isabelle

Abstract

Amniotic band syndrome (ABS) and limb body wall complex (LBWC) have an overlapping phenotype of multiple congenital anomalies and their etiology is unknown. We aimed to determine the prevalence of ABS and LBWC in Europe from 1980 to 2019 and to describe the spectrum of congenital anomalies. In addition, we investigated maternal age and multiple birth as possible risk factors for the occurrence of ABS and LBWC. We used data from the European surveillance of congenital anomalies (EUROCAT) network including data from 30 registries over 1980–2019. We included all pregnancy outcomes, including live births, stillbirths, and terminations of pregnancy for fetal anomalies. ABS and LBWC cases were extracted from the central EUROCAT database using coding information responses from the registries. In total, 866 ABS cases and 451 LBWC cases were included in this study. The mean prevalence was 0.53/10,000 births for ABS and 0.34/10,000 births for LBWC during the 40 years. Prevalence of both ABS and LBWC was lower in the 1980s and higher in the United Kingdom. Limb anomalies and neural tube defects were commonly seen in ABS, whereas in LBWC abdominal and thoracic wall defects and limb anomalies were most prevalent. Twinning was confirmed as a risk factor for both ABS and LBWC. This study includes the largest cohort of ABS and LBWC cases ever reported over a large time period using standardized EUROCAT data. Prevalence, clinical characteristics, and the phenotypic spectrum are described, and twinning is confirmed as a risk factor. [ABSTRACT FROM AUTHOR]

Published
2023
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8. Epidemiology of aplasia cutis congenita: A population-based study in Europe.

Author

Coi A, Barisic I, Garne E, Pierini A, Addor MC, Aizpurua Atxega A, Ballardini E, Braz P, Broughan JM, Cavero-Carbonell C, de Walle HEK, Draper ES, Gatt M, Häusler M, Kinsner-Ovaskainen A, Kurinczuk JJ, Lelong N, Luyt K, Mezzasalma L, Mullaney C, Nelen V, Odak L, O'Mahony MT, Perthus I, Randrianaivo H, Rankin J, Rissmann A, Rouget F, Schaub B, Tucker D, Wellesley D, Wiśniewska K, Yevtushok L, and Santoro M

Subjects
Infant, Newborn, Humans, Europe epidemiology, Skin, Ectodermal Dysplasia epidemiology, Ectodermal Dysplasia genetics, Limb Deformities, Congenital, Scalp Dermatoses
Abstract

Background: Aplasia cutis congenita (ACC) is a rare congenital anomaly characterized by localized or widespread absence of skin at birth, mainly affecting the scalp. Most information about ACC exists as individual case reports and medium-sized studies., Objectives: This study aimed to investigate the epidemiology of ACC, using data from a large European network of population-based registries for congenital anomalies (EUROCAT)., Methods: Twenty-eight EUROCAT population-based registries in 16 European countries were involved. Poisson regression models were exploited to estimate the overall and live birth prevalence, to test time trends in prevalence between four 5-year periods and to evaluate the impact of the change of coding for ACC from the unspecific ICD9-BPA code to the specific ICD10 code. Proportions of ACC cases associated with other anomalies were reported., Results: Five hundred cases were identified in the period 1998-2017 (prevalence: 5.10 per 100,000 births). Prevalence across 5-year periods did not differ significantly and no significant differences were evident due to the change from ICD9 to ICD10 in ACC coding. Heterogeneity in prevalence was observed across registries. The scalp was the most common site for ACC (96.4%) and associated congenital anomalies were present in 33.8% of cases. Patau and Adams-Oliver syndromes were the most frequent among the associated chromosomal anomalies (88.3%) and the associated genetic syndromes (57.7%), respectively. 16% of cases were associated with limb anomalies and 15.4% with congenital heart defects. A family history of ACC was found in 2% of cases., Conclusion: To our knowledge, this is the only population-based study on ACC. The EUROCAT methodologies provide reliable prevalence estimates and proportions of associated anomalies., (© 2022 European Academy of Dermatology and Venereology.)

Published
2023
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