Embriopatía por isotretinoína con microtia-anotia y cardiopatía. Presentación de un caso
نویسندگان
چکیده
منابع مشابه
Una aproximación dirigida por modelos para diseñar y construir esquemas XML: Un caso de estudio
In this ar ticle we show the usefulness of the model dr iven methodological framework called MIDAS for the transformation of conceptual schemas in UML (Platform Independent Model) to XML schemes (Platform Specific Model) by means of its application to a case study. In addition, the limitations that this methodological approach presents at the moment of gather ing ...
متن کاملPeripheral Spondyloarthritis in a Patient With Noonan’s Syndrome
Noonan’s syndrome is an autosomal dominant genetic disorder with high phenotypic variability, characterized mainly by facial dysmorphism, congenital heart disease and short stature. We describe the case of a male patient diagnosed with Noonan’s syndrome and peripheral spondyloarthritis, a previously undescribed association in the literature. © 2013 Elsevier España, S.L.U. All rights reserved. P...
متن کاملComunicación en las Organizaciones y TICs: Un Estudio de Caso
Resumen. Se plantea en base a la investigación empírica y la experiencias recolectadas, los elementos que se deben de considerar cuando se trata de invertir en herramientas de comunicación con el objetivo de facilitar la docencia y mejorar los resultados. El marco de referencia para presentar el caso en estudio es la Universidad de La Frontera. El estudio hace énfasis en los modelos de la comun...
متن کاملThe epidemiology of anotia and microtia.
We studied a large data set from three registries of congenital malformations (central-east France, Sweden, and California), a total of 954 cases, known chromosome anomalies excluded. The prevalence at birth varied significantly between programmes, probably to a large extent because of different ascertainment and inclusion criteria, from 0.76 per 10,000 births in the French programme to 2.35 in...
متن کاملIDientes de Capdepont - un Defecto de Dentina Hereditario. Reporte de Caso y Revisión de la Literatura
Dentinogenesis imperfecta is an autosomal dominant genetic disorder with abnormal dentin structure affecting both primary and permanent dentitions leading to discolouration and attrition of teeth. Diagnosis is usually based on family history, a detailed clinical examination and pedigree construction. Treatment involves preservation of teeth, removal of infection, restoration of function and est...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Archivos Argentinos de Pediatria
سال: 2012
ISSN: 0325-0075
DOI: 10.5546/aap.2012.e47