Atypical VACTERL Syndrome in an Infant: a Case Report from CHU Mere-Enfant Fondation Jeanne Ebori

MJ Myrtille, NM NJ, A Kinga, TL Midili, AK CP… - HEALTH SCIENCES …, 2023 - hsd-fmsb.org
Le syndrome de VACTERL est une association malformative polymorphe rare, qui intéresse
1/10.000 à 1/40.000 naissances vivantes. Le diagnostic repose sur la présence variable de …

[PDF][PDF] Significance of foetal autopsy in diagnosis of VACTERL association

JP Jessy, R Kumar, A Kaur, K Kapoor, M Sharma… - EJA, 2023 - researchgate.net
SUMMARY VACTERL association occurs in 1 in 10000-40000 live births and is associated
with vertebral defects, anal atresia, cardiac malformations, tracheoesophageal fistula, renal …

[HTML][HTML] Ассоциация VACTERL в практике врача-неонатолога

ЕА Саркисян, АП Хохлова, ИЮ Зяблова… - Лечащий …, 2024 - cyberleninka.ru
Введение. На сегодняшний день врожденные пороки развития занимают лидирующие
позиции в структуре заболеваемости и смертности детей в неонатальном периоде …

Actualización y revisión del síndrome de Vacterl

BBS Romina, TÁM Vinicio - Polo del Conocimiento: Revista …, 2023 - dialnet.unirioja.es
El síndrome o asociación de VACTERL tiene una baja incidencia de 1 a 10-40 mil nacidos
vivos con mayores casos presentados en varones, el diagnóstico prenatal oportuno es la …

[HTML][HTML] Left Nostril Agenesis in a Fetus with VACTERL Association: A Case Report

M Martínez-Gómez, E Satorres-Pérez… - Open Journal of …, 2023 - scirp.org
VACTERL association represents a rare condition with a broad spectrum of coexisting
congenital abnormalities. Although a multifactorial origin has been described, the etiology is …

Actualización y revisión del síndrome de Vacterl

SR Bravo Banda - 2023 - repositorio.uta.edu.ec
El síndrome o asociación de VACTERL tiene una baja incidencia de 1 a 10-40 mil nacidos
vivos con mayores casos presentados en varones, el diagnóstico prenatal oportuno es la …

[PDF][PDF] EKTOPIČAN KARLIČNI BUBREG DETETA–PRIKAZ SLUČAJA

J Miolski, J Marjanović, S Stanojević… - Medical Journal …, 2022 - researchgate.net
Uvod. Ektopičan karlični bubreg je anatomska anomalija u položaju bubrega. U fazi
metanefrosa izostaju njegovo kretanje, rotacija i podizanje iz karlice ka lumbalnoj loži. Zbog …

[PDF][PDF] Surgical Management of an Obstructive Müllerian Anomaly in a Patient with VACTERL Association: A Case Report

C Lavoie, M Au, H Syed, C Do, Z Baker… - Clin Case Rep Int … - clinicalcasereportsint.com
Background: The incidence of VACTERL association alone has been estimated at around 1
in 10,000 to 1 in 40,000 live born infants. Upon review of existing literature, few if any other …

Asocieri malformative rare. Split notochord sindrom (SNS)

O Utchina, V Boian, A Draganel - Chirurgie pediatrică–prezent și viitor, 2023 - ibn.idsi.md
Anorectal malformations are the most severe congenital malformations of the
gastrointestinal tract from the point of view of surgical correction and anatomo-functional …

Ektopičan karlični bubreg kod dece

J Miolski, J Marjanović, S Stanojević, N Didić… - Medicinski …, 2022 - aseestant.ceon.rs
Sažetak Uvod: Ektopičan karlični bubreg je anatomska anomalija u položaju bubrega. U fazi
metanefrosa izostaje njegovo podizanje i rotacija iz karlice u sakralnom delu kičme u …