A5072802218- Congenital Anomalies and Fetal Surgery
- Urological Disorders and Treatments
- Child and Adolescent Health
- Prenatal Screening and Diagnostics
- Nutrition and Health Studies
- Cleft Lip and Palate Research
- Childhood Cancer Survivors' Quality of Life
- Congenital limb and hand anomalies
- Hip disorders and treatments
- Parvovirus B19 Infection Studies
- Folate and B Vitamins Research
- Assisted Reproductive Technology and Twin Pregnancy
- Ectopic Pregnancy Diagnosis and Management
- Education and Cultural Studies
- Nonmelanoma Skin Cancer Studies
- Polish Historical and Cultural Studies
- Social Issues in Poland
- Hedgehog Signaling Pathway Studies
- Vascular Malformations and Hemangiomas
- Consumer Behavior and Market Dynamics
- Connective tissue disorders research
- Health, Work, and Social Studies in Poland
- Nutritional Studies and Diet
- Hair Growth and Disorders
- Cervical Cancer and HPV Research
Poznan University of Medical Sciences
2011-2022
National Center on Birth Defects and Developmental Disabilities
2019
Radom Academy of Economics
2015
Medical Genetics Center
2008-2011
General Department of Preventive Medicine
2008
Currently available data on the relationship between prevalence of isolated congenital malformations and parental age are inconsistent frequently divergent. We utilised from Polish Registry Congenital Malformations (PRCM) to accurately assess interplay maternal paternal in risk non-syndromic malformations. Out 902 452 livebirths we studied 8683 children aged 0-2 years registered PRCM. Logistic regression was used simultaneously adjust estimates for age. Our indicated that were independently...
Abstract Achondroplasia is a rare genetic disorder resulting in short‐limb skeletal dysplasia. We present the largest European population‐based epidemiological study to date using data provided by Surveillance of Congenital Anomalies (EUROCAT) network. All cases achondroplasia notified 28 EUROCAT registries (1991–2015) were included study. Prevalence, birth outcomes, prenatal diagnosis, associated anomalies, and impact paternal maternal age on de novo presented. The population consisted 434...
We aimed to assess prevalence, birth outcome, associated anomalies and prenatal diagnosis of congenital clubfoot in Europe using data from the EUROCAT network, validate recording as a major anomaly by registries. Cases were included 18 registries covering more than 4.8 million births 1995–2011. without chromosomal born during 2005–2009, randomly selected for validation questionnaire on diagnostic details treatment. There was 5,458 cases which 5,056 (93%) liveborn infants. Total prevalence...
We examined the relationship between maternal reproductive history and newborn's risk of isolated congenital malformations in a large case-control cohort from Polish Registry Congenital Malformations. were classified into four categories: heart defects (n=1673), cleft palate (n=255), lip with or without (n=448) renal agenesis (n=103). The case groups compared shared group 2068 controls recruited same time period geographic area. Multivariable logistic regression was used to assess associated...
Polydactyly represents a heterogeneous group of congenital hand and foot anomalies with variable clinical features diverse etiology. Preaxial polydactyly type I (PPD1) is the most frequent form preaxial polydactyly. The etiology sporadic PPD1 remains largely unknown relative contribution genetic environmental factors not clearly defined. primary goals this study are twofold: (1) to examine epidemiology in comparison healthy control group, (2) contrast characteristics familial forms isolated...
Objectives:The aims of this study were: to evaluate the prevalence abdominal wall defects in Polish population, analyze temporal trends prevalence, identify areas (clusters) high risk defects, and characterize, with respect epidemiology, children their mothers area defined as a cluster.Material Methods: We used isolated congenital malformations (gastroschisis Q79.3 omphalocele Q79.2 according International Statistical Classification Diseases Related Health Problems, 10th revision (ICD-10,...
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.This study aimed to investigate epidemiology ACC, using data from large European network population-based registries for anomalies (EUROCAT).Twenty-eight EUROCAT in 16 countries were involved. Poisson regression models exploited estimate overall live birth...
Abstract BACKGROUND: Amniotic rupture sequence (ARS) is a disruption presenting with fibrous bands, possibly emerging as result of amniotic tear in the first trimester gestation. Our comparative study aims to assess whether there difference clinical pattern congenital limb and internal organ anomalies between ARS body wall defect (ARS‐BWD) without BWD (ARS‐L). METHODS: Among 1,706,639 births recorded 1998 2006, 50 infants diagnosis were reported Polish Registry Congenital Malformations. The...
The goal of this analysis is to identify risk factors for infantile hemangiomas (IH) better delineate hemangioma predisposition. We analyzed live birth children with isolated cutaneous that were reported the Polish Registry Congenital Malformations from across Poland between years 1998 and 2016. Lower birthweight gestational age most significant associated IH. also observed a trend higher IH lower level maternal paternal education. Moreover, mothers have probability having child compared...
Geographic variation in the prevalence of isolated cleft lip with or without palate may be due to exogenous environmental factors genetic variation. In this study, we aim evaluate Polish urban and rural environments order identify geographic areas high (defect clusters).We use all cases congenital malformations reported Registry Congenital Malformations years 1998-2008 from total population 2,362,502 births.We detect a strong signal increased single region Poland, Dolnośląskie voivodeship....
Data from the Polish Registry of Congenital Malformations (PRCM) suggest that prevalence limb reduction defects (LRDs) in some regions is significantly higher comparison to reported European Surveillance Anomalies (EUROCAT) registry, but specific risk factors are still unknown. The objectives this study were two-fold: detect linked isolated LRDs among natives and search for geospatial clusters identify high-risk areas across country. Among 2,939,001 births accounted PRCM, we determined there...
1. Lieff S, Olshan AF, Werler M, Strauss RP, Smith J, Michell A. Maternal cigarette smoking during pregnancy and risk of oral clefts in newborns. Am J Epidemiol. 1999; 150: 683–694. Google Scholar
Wprowadzenie i cel: Rak jelita grubego (C18-C21) jest jednym z najczęściej występujących nowotworów złośliwych w polskiej populacji. Celem niniejszej pracy była analiza sytuacji epidemiologicznej raka Polsce, której dokonano na podstawie danych epidemiologicznych, opublikowanych przez Krajowy Rejestr Nowotworów, Narodowy Instytut Onkologii im. Marii Skłodowskiej-Curie – Państwowy Badawczy oraz ECIS European Cancer Information System. 
 Opis stanu wiedzy: był Polsce 2018 roku trzecim co...
According to the definition by Eurocat Working Group1 , a cluster of congenital malformation is an aggrega-1 EUROCAT European network population-based registries for epidemiologic surveillance anomalies, started in 1979.The Group on Management Clusters and Environmental Exposure Incidents has developed 2003.tion cases anomaly time and/or space which appears be unusual.The incidence such may caused local spatial relations.Fotheringham (1997Fotheringham ( [1], 2000 [2] [2]) distinguishes four...