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Books on the topic 'Congenital anomally'

Author: Grafiati

Published: 5 June 2025

Last updated: 2 August 2025

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1

Great Britain. Office for National Statistics., ed. Congenital anomaly statistics: Notifications : a statistical review of notifications of congenital malformations receivedas part of the England and Wales national congenital anomaly system. Stationery Office., 1997.

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2

Great Britain. Office for National Statistics. Congenital anomaly statistics: Notifications: a statistical review of notifications of congenital anomalies received as part of the England and Wales Congenital Anomaly System, 2001. Stationery Office, 2002.

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3

Hras̆ka, Viktor. Surgical management of congenital heart disease I: Complex transposition of great arteries right and left, ventricular outflow, tract obstruction, Ebsteins anomaly : a video manual. Springer, 2012.

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4

British Isles Network of Congenital Anomaly Registers. Congenital Anomaly Statistics 2010. Dandy Booksellers Ltd, 2013.

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5

Statistics, Office for National. Congenital Anomaly Statistics Notification. Palgrave Macmillan, 2006.

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6

Statistics, Office for National. Congenital Anomaly Statistics (Series MB3). Stationery Office Books, 1998.

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7

Statistics, Office for National. Congenital Anomaly Statistics (Series MB3). Stationery Office Books, 1999.

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8

The Office for National Statistics. Congenital Anomaly Statistics Notification 2007 No. 22. Palgrave Macmillan Limited, 2009.

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9

NA, NA. Congenital Anomaly Statistics Notification 2003 No. 18. Palgrave Macmillan, 2005.

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10

NA, NA. Congenital Anomaly Statistics Notification 2005 No. 20. Palgrave Macmillan, 2007.

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11

Tso. Congenital Anomaly Statistics: Notifications, 1997 (Series MB3). Stationery Office Books (TSO), 1999.

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12

Office for National Statistics Staff. Congenital Anomaly Statistics: Notifications - A Statistical Review of Notifications of Congenital Anomalies Received As Part of the England and Wales Congenital Anomaly System. Stationery Office, The, 2002.

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13

Office for National Statistics Staff. Congenital Anomaly Statistics: Notifications - A Statistical Review of Notifications of Congenital Anomalies Received As Part of the England and Wales Congenital Anomaly System. Stationery Office, The, 2001.

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14

Great Britain: Office for National Statistics. Congenital anomaly Statistics: Notifications, a statistical review of notifications of congenital anomalies received as part of the England and Wales National Congenital Anomaly System 2002. Stationery Office, The, 2004.

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15

Lancellotti, Patrizio, and Bernard Cosyns. Adult Congenital Heart Disease. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780198713623.003.0013.

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Echocardiography has a fundamental role in patients with adult congenital heart disease. This chapter identifies the role of echocardiography in atrial septal defects, ventricular septal defects, atrioventricular septal defects, patent ductus arteriosus, and persistent left superior vena cava. For each condition, the role of transthoracic and transoesophagael echocardiogram are shown alongside examples of main types and features and haemodynamic effect. Echocardiographic findings of LV outflow tract obstruction, supravalvular aortic stenosis, aortic stenosis, and aortic coarction are covered,

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16

Tso. Congenital Anomaly Statistics: Notifications 1999 (Opcs Series Mb3, 14). Stationery Office, 2001.

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17

Orchard, Liz. Congenital heart disease in adults. Edited by Patrick Davey and David Sprigings. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199568741.003.0088.

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Congenital heart disease is the most common congenital abnormality, affecting 0.8% of births. There have been major advances in both the surgical and interventional treatment of congenital heart disease, with about 85% of patients now surviving into adulthood. Congenital heart disease can be divided into simple and complex lesions. Simple lesions include atrial septal defect, ventricular septal defect, patent ductus arteriosus, coarctation of the aorta, and left ventricular outflow tract lesions. Complex lesions include tetralogy of Fallot, complete transposition of great arteries, single vent

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18

The national congenital anomaly system: A guide for users and suppliers. Office for National Statistics, 1999.

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19

Thorne, Sara, and Paul Clift, eds. Rare conditions presenting in adulthood. Oxford University Press, 2011. http://dx.doi.org/10.1093/med/9780199228188.003.0026.

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Coronary anomalies 190Sinus of valsalva aneurysm 192 See Table 15.1.• Rare.• Occur in isolation or with associated congenital cardiac lesions.• Clinical significance depends on potential of the anomaly to cause ischaemia and sudden death.• Ischaemia is main indication for surgical repair and is associated with:...

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20

Congenital Uterine Anomalies: Education for Patients and the Public. Exon Publications, 2025. https://doi.org/10.36255/congenital-uterine-anomalies-patient-public-education.

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Congenital uterine anomalies are birth-related abnormalities in the structure of the uterus that may impact menstrual health, fertility, or pregnancy outcomes. These conditions arise during fetal development when the uterus does not form correctly. Some women may have no symptoms at all, while others discover the condition during evaluation for infertility or recurrent pregnancy loss. This article explains in clear language what congenital uterine anomalies are and outlines the different types, such as septate, bicornuate, and didelphys uterus. It describes how these structural differences occ

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21

Lee, Ryan W. Smith-Lemli-Opitz Syndrome. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199937837.003.0078.

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Smith-Lemli-Opitz syndrome (OMIM 270400) (SLOS) is a multiple congenital anomaly disorder caused by an inborn error of cholesterol synthesis. Studies demonstrated that mutations in the gene for 3b-hydroxysterol-D7 reductase (DHCR7) result in low plasma cholesterol and corresponding increases in 7DHC. Distinctive facial features of include ptosis, small nose with anteverted nares, and micrognathia. Acral dysgenesis is common, foremost of which involve syndactyly and polydactyly. Children with SLOS often have a behavioral phenotype within the autism spectrum.

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22

Thorne, Sara, and Sarah Bowater. Valve and outflow tract lesions. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780198759959.003.0008.

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This chapter discusses valve and outflow tract lesions. It considers left ventricular outflow tract obstruction (LVOTO), including subvalvar aortic stenosis (AS), bicuspid aortic valve, and supravalvar AS. Also discussed are left ventricular inflow lesions, including congenital mitral valve abnormalities, cor triatriatum, and Shone syndrome. It also covers right ventricular outflow tract obstruction (RVOTO), including pulmonary valvar stenosis, supravalvar pulmonary stenosis, pulmonary artery stenosis, pulmonary atresia with intact septum, and double-chambered right ventricle. Ebstein anomaly

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23

Hraska, Viktor, and Peter Murin. Surgical Management of Congenital Heart Disease I: Complex Transposition of Great Arteries Right and Left Ventricular Outflow Tract Obstruction Ebstein's Anomaly A Video Manual. Springer, 2017.

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24

Hraska, Viktor, and Peter Murin. Surgical Management of Congenital Heart Disease I: Complex Transposition of Great Arteries Right and Left Ventricular Outflow Tract Obstruction Ebstein´s Anomaly A Video Manual. Springer, 2012.

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25

Mariani, Giulia Adalgisa. Varianti anatomiche. Bononia University Press, 2020. http://dx.doi.org/10.30682/alph06.

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Con il termine variante anatomica si definisce una particolare struttura anatomica la cui morfologia si discosta da quella osservata nella maggior parte degli individui. Diversamente dalle anomalie congenite, che per definizione sono considerate patologiche, le varianti rientrano in un quadro di normalità. È però evidente che conformazioni anatomiche peculiari possono interferire con le procedure diagnostiche e aumentare il rischio di complicanze durante gli interventi chirurgici. La conoscenza dell’anatomia umana e lo studio delle sue varianti rappresentano perciò un requisito indispensabile

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