Vacterl/vater association

BD Solomon - Orphanet journal of rare diseases, 2011 - Springer
VACTERL/VATER association is typically defined by the presence of at least three of the
following congenital malformations: vertebral defects, anal atresia, cardiac defects, tracheo …

Congenital anomalies of the tracheobronchial tree, lung, and mediastinum: embryology, radiology, and pathology

T Berrocal, C Madrid, S Novo, J Gutiérrez, A Arjonilla… - Radiographics, 2004 - pubs.rsna.org
Congenital anomalies of the chest are an important cause of morbidity in infants, children,
and even adults. The evaluation of affected patients frequently requires multiple imaging …

Etiology and clinical presentation of birth defects: population based study

ML Feldkamp, JC Carey, JLB Byrne, S Krikov, LD Botto - bmj, 2017 - bmj.com
Objective To assess causation and clinical presentation of major birth defects. Design
Population based case cohort. Setting Cases of birth defects in children born 2005-09 to …

Oesophageal atresia, tracheo-oesophageal fistula, and the VACTERL association: review of genetics and epidemiology

C Shaw-Smith - Journal of medical genetics, 2006 - jmg.bmj.com
Oesophageal atresia and/or tracheo-oesophageal fistula are relatively common
malformations occurring in approximately 1 in 3500 births. In around half of the cases …

Resorbable bioscaffold for esophageal repair in a dog model

S Badylak, S Meurling, M Chen, A Spievack… - Journal of pediatric …, 2000 - Elsevier
Purpose: Porcine-derived, xenogeneic extracellular matrix (ECM) derived from either the
small intestinal submucosa (SIS) or urinary bladder submucosa (UBS) was used as a tissue …

The Mayer-Rokitansky-Küster-Hauser syndrome (congenital absence of uterus and vagina)–phenotypic manifestations and genetic approaches

D Guerrier, T Mouchel, L Pasquier, I Pellerin - Journal of negative results …, 2006 - Springer
Abstract The Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome affects at least 1 out of
4500 women and has for a long time been considered as a sporadic anomaly. Congenital …

One hundred three consecutive patients with anorectal malformations and their associated anomalies

S Cho, SP Moore, T Fangman - Archives of pediatrics & …, 2001 - jamanetwork.com
Objective A long-term retrospective analysis of 103 infants with anorectal malformations
(ARMs) was conducted to describe any associated congenital anomalies and surgical …

Sirenomelia: an epidemiologic study in a large dataset from the International Clearinghouse of Birth Defects Surveillance and Research, and literature review

IM Orioli, E Amar, J Arteaga‐Vazquez… - American Journal of …, 2011 - Wiley Online Library
Sirenomelia is a very rare limb anomaly in which the normally paired lower limbs are
replaced by a single midline limb. This study describes the prevalence, associated …

Spectrum of congenital anomalies in pregnancies with pregestational diabetes

E Garne, M Loane, H Dolk, I Barisic… - … Research Part A …, 2012 - Wiley Online Library
BACKGROUND Maternal pregestational diabetes is a well‐known risk factor for congenital
anomalies. This study analyses the spectrum of congenital anomalies associated with …

Anorectal anomalies associated with or as part of other anomalies

A Cuschieri… - American journal of …, 2002 - Wiley Online Library
Anorectal anomalies occurring with other anomalies or as part of syndromes were analyzed
to determine how their epidemiological characteristics differed from those of isolated anal …