Results 31 to 40 of about 1,312,947 (193)

Diaphragmatic Hernia as a Prenatal Feature of Glycosylphosphatidylinositol Biosynthesis Defects and the Overlap With Fryns Syndrome – Literature Review

Frontiers in Genetics, 2021
Fryns syndrome is an autosomal recessive multiple congenital anomaly syndrome, with diaphragmatic defects and secondary lung hypoplasia as cardinal features. Despite it was reported first in 1979, its exact etiology has not been established to date. With
Przemyslaw Kosinski, Milena Greczan, Aleksandra Jezela-Stanek   +2 more
doaj   +1 more source

Proximal Interruption of the Pulmonary Artery: A Case Series [PDF]

Journal of Clinical and Diagnostic Research, 2015
We present a few cases of Proximal Interruption of the Pulmonary Artery, an uncommon developmental anomaly associated with congenital heart disease. The cases had varied clinical presentations.
S.H. Anand, Anitha Jasper, Sunithi Elizabeth Mani, Elizabeth Joseph, John Mathai   +4 more
doaj   +1 more source

Geographic variation and localised clustering of congenital anomalies in Great Britain [PDF]

, 2007
Background Environmental pollution as a cause of congenital anomalies is sometimes suspected because of clustering of anomalies in areas of higher exposure.
Grundy C, Wellesley, D, Loane, M, Dolk Helen, Rankin Judith, Loane Maria, Rankin, Judith, Stone David, Loane M, Wellesley, D., Stone, D, Abramsky L, Stone, David, Pattenden, S., Armstrong, B.G., Dunn, C.E., Pattenden S, Armstrong BG, Armstrong, Ben G, Dolk, H, Dolk, H., Armstrong Ben G, Grundy, C., Boyd Patricia A, Boyd, Patricia A, Armstrong, B, Rankin, J., Boyd, P, Dunn, Chris E, Dunn CE, Loane, M., Wellesley, Diana, Boyd PA, Vrijheid, M., Stone, D., Grundy Chris, Vrijheid Martine, Dolk H, Abramsky, L, Stone D, Abramsky, Lenore, Abramsky Lenore, Vrijheid M, Grundy, C, Vrijheid, Martine, Grundy, Chris, Dolk, Helen, Boyd, P.A., Pattenden Sam, Wellesley Diana, Pattenden, Sam, Wellesley D, Dunn Chris E, Abramsky, L., Dunn, C, Pattenden, S, Boyd, P., Loane, Maria, Rankin J, Rankin, J   +59 more
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Number of publications per type of congenital anomaly.

, 2023
Number of publications per type of congenital anomaly.
Caroline Osoro (16462479), Nkwati Michel Maboh (13531332), Linda Barlow-Mosha (3389495), Ieda Orioli (16462470), Ushma Mehta (59853), Phylis Kisa (16462464), Ronald Kusolo (13200268), Lorenzo D. Botto (9420518), Hamisi Kimaro Shabani (16462485), Philippa Musoke (224519), Daniel Mumpe-Mwanja (10258516), Robert Serujogi (16462473), Idowu Ayede (16462467), Helen Dolk (3169182), Aminkeng Zawuo Leke (13531329), Clarisse Dah (10321042), Helen Malherbe (16462461), Bodo Bongomin (16462476), Emma Kalk (2226307), Rebecca Zash (3860278), Olive Sentumbwe–Mugisha (16462482), Lee Fairlie (355761)   +21 more
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Surgical management of congenital lung anomalies

Srpski arhiv za celokupno lekarstvo, 2004
Prenatal diagnosis allows for insight into the evaluation of fetal lung anomalies. Serial ultrasonographic studies of fetuses helped in evaluation and definition of the natural course of these lesions as well as necessity for fetal therapy. It has been found that the overall prognosis depends on the size of the lung mass and the secondary ...
Marija Lukac, Sanja Sindjic, Zoran Krstic, Aleksandar Ljubic, Zeljko Smoljanic, Polina Pavicevic, Svjetlana Maglajlic, Dragana Vujovic, Radoslav Lukac   +8 more
openaire   +1 more source

Risk of congenital anomaly in relation to residence near hazardous waste landfill sites. [PDF]

The main aim of this thesis is to investigate whether residence near hazardous waste landfill sites is associated with an increased risk of congenital anomaly.
Vrijheid, Martine
core   +1 more source

Bilobed gallbladder: a rare congenital anomaly of the biliary system [PDF]

, 2021
Duplication of the gallbladder is a rare congenital anomaly, which Boyden first illustrated in 1926. No additional risk of cholelithiasis or malignancy with this congenital anomaly was documented.
Saini, Aditi, Verma, Prashant Kumar, Syed, Anjum, Agarwal, Srishti, Roul, Pradeep Kumar, Srishti Agarwal, Pradeep Kumar Roul, Aditi Saini, Anjum Syed, Prashant Kumar Verma   +9 more
core   +1 more source

CT features of lung agenesis – a case series (6 cases)

BMC Medical Imaging, 2018
Back ground Lung agenesis is a rare congenital anomaly. The main etiology of the disease is unknown whereas genetic, iatrogenic and viral factors as well as vitamin A deficiency during early pregnancy may result in developmental failure of primitive lung
Jamshid Sadiqi, Hidayatullah Hamidi
doaj   +1 more source

Case Report: Transcatheter treatment of aortic coarctation in a 58-year-old patient with LACHT syndrome and left lung agenesis

Frontiers in Cardiovascular Medicine, 2023
LACHT (Lung Agenesis, Congenital Heart, and Thumb anomalies) syndrome is an extremely rare congenital anomaly and presents significant challenges in adults due to its poor survival rates.
Qingxian Tu, Nanqu Huang, Fujia Guo, Minhong Luo, Min Xu, Jiaji Liu, Zhengqiang Yuan, Qianfeng Jiang   +7 more
doaj   +1 more source

3 year old with chronic wet cough : Intralobar Bronchopulmonary sequestration [PDF]

, 2016
Bronchopulmonary sequestration (BPS) is a rare congenital foregut anomaly of the lung, consisting of nonfunctioning primitive tissue that does not communicate with the healthy tracheobronchial tree.
Micallef, S.P., Sammut, Patrick, DeGiovanni, Joseph V., Grech, Victor E.   +3 more
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