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The VACTERL association (also VATER association, and less accurately VACTERL syndrome) refers to a recognized group of birth defects which tend to co-occur (see ). This pattern is a recognized association, as opposed to a syndrome, because there is no known pathogenetic cause to explain the grouped incidence. No specific genetic or chromosome problem has been identified with VACTERL association. VACTERL can be seen with some chromosomal defects such as Trisomy 18 and is more frequently seen in babies of diabetic mothers. VACTERL association, however, is most likely caused by multiple factors.

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  • متلازمة فاكترل (ar)
  • VACTERL-Assoziation (de)
  • Síndrome de VACTERL (es)
  • VATERL sindrome (eu)
  • Syndrome de VACTERL (fr)
  • Sindrome di VATER (it)
  • Asocjacja VACTERL (pl)
  • Associação VACTERL (pt)
  • Ассоциация VACTERL (ru)
  • VACTERL association (en)
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  • متلازمة فاكترل أو فاتر هي متلازمة تتميز بعيوب خلقية معينة، توجد ثلاثة منها على الأقل في الجنين: عيوب الفقرات، رتق الشرج، عيوب خلقية في القلب، ناسور قصبي مريئي، عيوب الكلى وعيوب الأطراف. (ar)
  • El VACTERL es una asociación de alta frecuencia, es decir, un conjunto de múltiples anomalías que no pueden catalogarse como un síndrome y que se presentan en al menos dos individuos y que no pueden atribuirse al azar. Se trata de una enfermedad extremadamente rara del desarrollo embrionario que afecta a diversas estructuras y vísceras del cuerpo humano.[cita requerida] (es)
  • Le syndrome de VACTERL (ou « association VACTERL ») est un ensemble d'anomalies congénitales ou malformations, qui ne répondent à aucun critère précis de regroupement, mais qui n'apparaissent pas non plus de manière aléatoire.C'est une extension du syndrome de VATER. (fr)
  • Ассоциация VACTERL — группа сочетанных аномалий развития. Название VACTERL составлено из первых букв пороков, входящих в состав синдрома: * V (англ. Vertebral anomalies) — аномалии позвоночника (70 %), * А (англ. Anal аtresia) — атрезия ануса (55 %), * С (англ. Cardiovascular anomalies) — дефекты перегородок и другие пороки сердца (75 %), * ТЕ (англ. Tracheo-esophageal fistula) — трахеопищеводный свищ с атрезией пищевода (70 %), * R (англ. Renal defects) — аномалии почек (50 %) — агенезия, дисплазия, гидронефроз; единственная пупочная артерия. * L (англ. Limb defects) — дефекты лучевой кости — гипоплазия I пальца или лучевой кости, преаксиальная полидактилия и синдактилия (70 %); (ru)
  • Die Bezeichnung VACTERL-Assoziation fasst eine Kombination komplexer Fehlbildungen auf dem Boden embryonaler, möglicherweise autosomal-rezessiv vererbter Entwicklungsstörungen zusammen. VACTERL ist ein Acronym, das die möglichen Fehlbildungen beschreibt: Hat ein Kind mindestens drei dieser Fehlbildungen, wird es medizinisch gesehen zur Gruppe der Kinder mit VACTERL-Assoziation gerechnet, synonym gebräuchlich ist auch VATER-Syndrom. (de)
  • edo VACTERL elkartzea (GNS:Q87.2) sortzetiko malformazioen ez-randomizaturiko elkartzea da. Sindrome baino asoziazio edo elkartze deitzearen arrazoia gaixotasun hauekin loturiko geneak ez ezagutzea da. Izena ingelesezko akronimoan du jatorria eta ohikoen diren sortzetiko akatsak deskribatzen ditu: Gaixo bakoitzak duen sintoma multzoen konbinaketa bakarra da, beste gaixoetatik bereizituz. Kausak edo arrazoiak oraindik eztabaidan daude, baina ziurrenik jatorri multifaktoriala izango du: (eu)
  • The VACTERL association (also VATER association, and less accurately VACTERL syndrome) refers to a recognized group of birth defects which tend to co-occur (see ). This pattern is a recognized association, as opposed to a syndrome, because there is no known pathogenetic cause to explain the grouped incidence. No specific genetic or chromosome problem has been identified with VACTERL association. VACTERL can be seen with some chromosomal defects such as Trisomy 18 and is more frequently seen in babies of diabetic mothers. VACTERL association, however, is most likely caused by multiple factors. (en)
  • La sindrome di VATER è un'associazione di difetti congeniti. È infatti anche chiamata associazione di VACTERL, dalle iniziali dei difetti, perché tutti i difetti sono connessi tra loro. Tuttavia è ancora sconosciuto il gene o il set genico che la causa. Alcuni individui presentano Trisomia 18, e si è notata una frequenza maggiore in figli di madri presentanti diabete.È a ogni modo preferita la tesi che sia dovuta a una serie di fattori concomitanti. (it)
  • Asocjacja VACTERL (ang. VACTERL association) – skojarzenie (asocjacja) wad wrodzonych; angielskie nazwy możliwych wad wchodzących w skład tej asocjacji tworzą akronim VACTERL i są to: * V – wady kręgów (ang. vertebral anomalies) * A – atrezja odbytu (anal atresia) * C – wrodzone wady serca (cardiac abnormalities) * T – przetoka tchawiczo-przełykowa (tracheo-esophagal fistula) * E – atrezja przełyku (esophagal atresia) * R – wady nerek (renal abnormalities) albo dysplazja kości promieniowej (radial dysplasia) * L – wady kończyn (limb abnormalities). (pl)
  • A associação ou síndrome de VACTERL (VATER) é uma associação não-aleatória de defeitos congênitos. Embora todos esses defeitos estejam ligados, ainda é desconhecido o gene ou o grupo de genes que causam essas malformações de nascença, razão para se chamar essa desordem, preferencialmente, de "associação", ao invés de "síndrome". As causas dessa associação são discutidas. A associação VACTERL pode estar ligada a outras condições semelhantes, como a Síndrome de Klippel-Feil ou de Goldenhar, inclusive a cruzamentos de condições. (pt)
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  • VACTERL association (en)
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  • VACTERL association (en)
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  • http://commons.wikimedia.org/wiki/Special:FilePath/VACTERL.jpg
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