Phenotypic characteristics and copy number variants in a cohort of colombian patients with vacterl association

OM Moreno, AI Sánchez, A Herreño, G Giraldo… - Molecular …, 2020 - karger.com
… Each specific birth defect is provided in Figure 1. Fourteen of … VACTERL association spectrum,
with a nonspecific pattern of VACTERL-type birth defects, including genital abnormalities, …

Exome survey of individuals affected by VATER/VACTERL with renal phenotypes identifies phenocopies and novel candidate genes

CM Kolvenbach, AT van der Ven… - American Journal of …, 2021 - Wiley Online Library
… with VATER/VACTERL and comprises a large spectrum of … association. A potential link
between the cholesterol pathway… congenital malformations resembling the VATER/VACTERL

Stillborn infants: associated malformations

LB Holmes, H Nasri, R Beroukhim, AT Hunt… - … Defects Research, 2018 - Wiley Online Library
… in stillborn infants was more severe than the spectrum of abnormalities … Multiple congenital
anomalies ? etiology … to the types of heart defects identified in this study (Tables 1 and 2). …

Substantial incidence of bladder dysfunction in patients with VACTERL association: Implications for surveillance

A Gomes, LF Zapata, CI Galarreta… - American Journal of …, 2024 - Wiley Online Library
… , the spectrum of anomalies was broadened … VACTERL association does not have a specific
ICD-10 code, we used the codes Q87.89 (other specified congenital malformation syndrome

Prenatal imaging of anorectal malformations—10-year experience at a tertiary center in Switzerland

L Rohrer, Y Vial, C Gengler, E Tenisch, L Alamo - Pediatric radiology, 2020 - Springer
… Anorectal malformation is a complex spectrum of congenital defects of the distal bowel …
associated anomalies; three had a VACTERL association and two a caudal regression syndrome. …

[HTML][HTML] Cancer incidence and spectrum among children with genetically confirmed Beckwith-Wiedemann spectrum in Germany: a retrospective cohort study

…, S Döhnert, C Kraus, G Kadgien, I Vater… - British Journal of …, 2020 - nature.com
Background Beckwith-Wiedemann syndrome (BWS) is a cancer predisposition syndrome
caused by defects on chromosome 11p15.5. The quantitative cancer risks in BWS patients …

Ear anomalies and hearing loss in patients with VACTERL association and the effect of maternal diabetes

CI Galarreta, E Hoyt, L Forero… - American Journal of …, 2023 - Wiley Online Library
… of VACTERL/VATER association involves a minimum of three congenital malformations
expression in patients with the VACTERL association spectrum. A possible explanation of this …

The DATE association: a separate entity or a further extension of the VACTERL association?

S Ceccanti, P Midrio, M Messina, G Mattioli… - … of surgical research, 2019 - Elsevier
birth defect, occurring in about 1 of every 4000 births worldwide. Although this spectrum of
malformations can … at least another birth defect, among which cardiac anomalies are the most …

[HTML][HTML] Developmental basis of trachea-esophageal birth defects

NA Edwards, V Shacham-Silverberg, L Weitz… - Developmental …, 2021 - Elsevier
… ), are a spectrum of life-threatening congenital anomalies in which the … Up until recently, the
developmental basis of these … of a syndrome in association with other defects (eg. VACTERL

Genetic counseling and diagnostics in anorectal malformation

C Marcelis, G Dworschak, I de Blaauw… - European Journal of …, 2021 - thieme-connect.com
… They separated the VACTERL patients in three groups: The STRICT-VACTERL
VACTERL-PLUS patients have an additional major congenital anomaly outside the VACTERL