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Translucencia Nucal, El Marcador Ecografico de I Trimestre de Embarazo

Translucencia Nucal, El Marcador Ecografico de I Trimestre de Embarazo

          
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About the Book

Tenemos el gran placer de presentar este libro sobre la Translucencia Nucal, considerado el mejor marcador ecográfico fetal para el cribado de cromosomopatías fetales en I trimestre de embarazo. Desde la primera observación llevada a cabo hace más de 100 años por el Dr. Langdon Down, que en 1866 constató que la piel de individuos afectados por la trisomía 21 parecía estar en exceso en la región cervical, hasta 1990, año en el que Szabo y Gellen describieron por primera vez en la literatura, trabajo publicado en The Lancet, la presencia de líquido subcutáneo en la región nucal, a partir de la semana 10 de embarazo, de un feto afecto de síndrome de Down, ya han pasado más de dos décadas. Cuando en 1992 Nicolaides propuso su uso como método de cribado en el primer trimestre, denominándola Translucencia Nucal (TN), es decir, el grosor ecograficamente anecoico (fluido), entre la parte externa del hueso occipital y la parte interna de la piel a nivel de la nuca del feto. Fue tal el impacto de esta herramienta de la ultrasonografía diagnóstica que generalmente asociamos este examen con screening de aneuploidías. de tal modo que hoy día la TN aumentada entre las semanas 11 y 14 es el marcador ultrasonográfico más efectivo para la detección de trisomía 21 y otras alteraciones cromosómicas y patología fetales.Desde entonces, son muchas las publicaciones existentes sobre este marcador ecográfico, pero no hemos podido encontrar ningún tratado sobre el mismo. Por ello, y con la magnífica colaboración de un grupo de expertos, nos propusimos elaborar este libro, que hoy, y tras mucho esfuerzo de todos, ve la luz.Hemos elaborado un índice ambicioso, en el que tuviera cabida todo lo relacionado con la Translucencia Nucal Fetal, su detallada medida, basada en una precisa metodología con una estandarización perfectamente establecida, siguiendo las guías de la Fetal Medical Foundation (FMF). También, los problemas prácticos que pueden surgir con su medida, su diagnóstico diferencial, el manejo adecuado ante una TN aumentada en un feto con cariotipo normal, la trascendencia que tiene el cribado combinado de cromosomopatías, y los controles de calidad existentes al respecto. Agradecemos a los editores invitados y a todos los amigos y colegas de Iberoamérica que han colaborado en este libro, muchas gracias por su tiempo y dedicación. También a José Manuel Padilla, por su esmerado trabajo de maquetación y diseño. Esperamos que les guste y que sea de gran utilidad práctica para todos aquellos que nos dedicamos al apasionante mundo de la Medicina Fetal y Perinatal.


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Product Details
  • ISBN-13: 9781731530967
  • Publisher: Independently Published
  • Publisher Imprint: Independently Published
  • Height: 279 mm
  • No of Pages: 176
  • Series Title: Colección de Libros Dr. Manuel Gallo Y Cols
  • Weight: 580 gr
  • ISBN-10: 173153096X
  • Publisher Date: 08 Dec 2018
  • Binding: Paperback
  • Language: Spanish
  • Returnable: N
  • Spine Width: 12 mm
  • Width: 216 mm


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