Zobrazeno 1 - 10
of 154
pro vyhledávání: '"Cns anomalies"'
Autor:
Behnaz Moradi, Fatemeh Zare Bidoki, Javid Azadbakht, Mahboobeh Shirazi, Hassan Hashemi, Sedigheh Hantooshzadeh, Mohamad Ali Kazemi, Mohammad Shafiee, Mohammad Hossein Golezar
Publikováno v:
Neurology Letters, Vol 3, Iss 1, Pp 12-19 (2024)
Background: This study is aimed to compare the accuracy of prenatal standard brain ultrasound (US), neurosonography (NSG), and magnetic resonance imaging (MRI) for diagnosing central nervous system (CNS) anomalies.Methods: In this prospective study p
Externí odkaz:
https://doaj.org/article/022d711f6be1402e9267504d189522b0
Publikováno v:
Egyptian Journal of Medical Research, Vol 4, Iss 1, Pp 83-96 (2023)
Background: Great concerns have been obtained for CNS anomalies due to their maternal and fetal morbidities and mortality outcomes. The high prevalence of CNS anomalies has been linked to polyhydramnios in several studies. This study was conducted to
Externí odkaz:
https://doaj.org/article/59a29d39d46348149ff0b9d7661820ef
Autor:
C. Falamesca, S. Cappelletti, R. Vicario, P.G. Amante, C. Correale, F. Vigevano, L. Caforio, T. Grimaldi Capitello
Publikováno v:
European Psychiatry, Vol 65, Pp S616-S617 (2022)
Introduction Women receiving a prenatal diagnosis of fetal anomalies are a high-risk population for psychological distress leading to mood disorders. Even so, to date we have no evidence of studies who investigated the levels of maternal anxiety and
Externí odkaz:
https://doaj.org/article/e711b02f272648fe967520d0ad254c40
Autor:
Emanuela Ponzi, Mattia Gentile, Emanuele Agolini, Emilia Matera, Roberto Palumbi, Antonia Lucia Buonadonna, Antonia Peschechera, Alessandra Gabellone, Maria Fatima Antonucci, Lucia Margari
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 7, Pp n/a-n/a (2020)
Abstract Background Chromosome 14q11‐q22 deletion syndrome (OMIM 613457) is a rare contiguous gene syndrome. Two regions of overlap (RO) of the 14q12q21.1 deletion have been identified: a proximal region (RO1), including FOXG1(*164874), NKX2‐1(*6
Externí odkaz:
https://doaj.org/article/c7a6e4f8e868449b82fdc9a74d62ed1f
Publikováno v:
Journal of Medical and Biological Engineering. 41:881-887
Congenital anomalies, also known as birth defects have been the primary focus of a number of studies globally. Our primary objective is to evaluate the significance of MRI in the prenatal diagnosis of congenital central nervous system (CNS) anomalies
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4892ed1022a281ebcea5d6d4fd4f765d
https://doi.org/10.1007/s40846-021-00657-5
https://doi.org/10.1007/s40846-021-00657-5
Autor:
Maayke A. de Koning, Emilia K. Bijlsma, Esther A. R. Nibbeling, Phebe N. Adama‐Scheltema, E J T Joanne Verweij, Cacha M.P.C.D. Peeters-Scholte, Mariëtte J.V. Hoffer, Marieke B. Veenhof, Gijs W. E. Santen, Menno J. P. Toirkens
Publikováno v:
Clinical Genetics, 101(1), 65-77. WILEY
Prenatal exome sequencing (pES) is a promising tool for diagnosing genetic disorders when structural anomalies are detected on prenatal ultrasound. The aim of this study was to investigate the diagnostic yield and clinical impact of pES as an additio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6ba07cbba6c9e2fac274ebaa0db86665
https://hdl.handle.net/1887/3249467
https://hdl.handle.net/1887/3249467
Autor:
Tootoonchi P "
Publikováno v:
Acta Medica Iranica, Vol 41, Iss 1, Pp 15-19 (2003)
To determine easily identifiable congenital anomalies (CA) prevalence and risk factors in the first 24 hours of life in a cross-sectional study we assessed 2291 live born neonates at four teaching hospitals from September 1999 until March 2000 in the
Externí odkaz:
https://doaj.org/article/cc337efe63c34370900e84277ecdd7a3
Autor:
Catherine Rodríguez, Sandra Valencia, Jorge Holguín, Karen Sarmiento, Shirly Puentes, Bibiana Deáquiz, Paula Hurtado-Villa, Sofía Páez, Valentina García, Ignacio Zarante
Publikováno v:
Pediatría. 52:61-68
Antecedentes en Colombia para el 2015 las anomalías del Sistema Nervioso Central (SNC) constituyeron el 16% de la mortalidad por anomalías congénitas, una tasa de sobrevida alta que genera cronicidad en el manejo del paciente y aumento en la carga
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::be851d3c66713b392d6a5db4c38e769f
https://doi.org/10.14295/p.v52i3.138
https://doi.org/10.14295/p.v52i3.138
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-12 (2021)
Scientific Reports
Scientific Reports
Etiopathogenesis of fetal ventriculomegaly is poorly understood. Associations between fetal isolated ventriculomegaly and copy number variations (CNVs) have been previously described. We investigated the correlations between fetal ventriculomegaly—
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::269c076ef0d4b77d7d0e92d8b447e704
https://doi.org/10.1038/s41598-021-83147-7
https://doi.org/10.1038/s41598-021-83147-7
Publikováno v:
Ultrasound in Obstetrics & Gynecology
OBJECTIVES There were two objectives of this study. First, to examine the value of uterine artery pulsatility index (UtA-PI) at 19-24 weeks' gestation in the prediction of subsequent development of pre-eclampsia (PE) and to compare the performance of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0edde0556ba823521b7209e552226d6a
https://pubmed.ncbi.nlm.nih.gov/33645854
https://pubmed.ncbi.nlm.nih.gov/33645854