Results 61 to 70 of about 46,412 (209)
Fístulas enterovesicales adquiridas
Se analiza una serie de 12 pacientes portadores de fístulas enterovesicales adquiridas en un período comprendido entre 1990 y 2002. Se consideran aspectos etiológicos, de la presentación clínica y paraclínica, y de las conductas terapéuticas confrontando
Carlos Barberousse +2 more
doaj
ABSTRACT Fanconi Anemia (FA) is the most frequent inherited bone marrow failure syndrome. A role for the XRCC2 gene in FA was suspected in 2012 and confirmed in 2016, but only two affected individuals have been described thus far, and no long‐term follow‐up is available.
Sabina Cenciarelli +11 more
wiley +1 more source
El objetivo de esta revisión pictográfica es la evaluación de las fístulas anorrectales mediante resonancia magnética. Esta técnica ha demostrado ser altamente confiable para estudiar la anatomía de la región perianal.
Pablo Soffia S +6 more
doaj
ABSTRACT Vascular Ehlers–Danlos syndrome (vEDS) is a hereditary connective tissue disorder caused by heterozygous pathogenic variants in COL3A1. European studies have shown that celiprolol may reduce the risk of life‐threatening vascular events, but outcomes in non‐European populations and the therapy's psychological impact remain unclear. We conducted
Megumi Furuhata‐Yoshimura +2 more
wiley +1 more source
Stents en fístulas esofagogástricas postquirúrgicas: in medio virtus
Rodrigo Castaño Llano
doaj +1 more source
[Objectives] To analyze the clinical data of patients with complex high anal fistulas having supralevator rectal opening (SRO), aiming to provide valuable insights for the clinical management of these patients.
Hu Jiansheng, Wang Wen, Sun Linmei
doaj +1 more source
FÍSTULAS DUODENAIS TARDIAS EM TRANSPLANTE PANCREÁTICO COM DRENAGEM VESICAL TRATADAS SEM CONVERSÃO
O uso da drenagem vesical inicialmente aumentou a segurança do transplante pancreático, porém, ao preço de um aumento da morbidade. Fístulas urinárias relacionadas principalmente ao coto duodenal, apesar de pouco freqüentes, ainda são controversas ...
João Eduardo Nicoluzzi +2 more
doaj +1 more source
Expanded Phenotype Associated With an Intronic PPP1R12A Variant: A Case Report and Literature Review
ABSTRACT Autosomal dominant PPP1R12A‐related genitourinary and/or brain malformation syndrome is a recently described multisystem disorder caused by loss‐of‐function variants in the protein phosphatase 1 regulatory subunit 12a (PPP1R12A) gene. To date, 22 affected individuals have been reported with variable brain malformations and genitourinary ...
Emily M. Bland +4 more
wiley +1 more source
Co‐Occurring Non‐Cardiac Congenital Anomalies Among Cases With Congenital Heart Defects
ABSTRACT Cases with congenital heart defects (CHD) often have other associated anomalies. The aim of this investigation was to assess the prevalence and the types of co‐occurring anomalies in CHD in a well‐defined population. The anomalies co‐occurring with CHD were ascertained in all live births, stillbirths and terminations of pregnancy for fetal ...
Claude Stoll +2 more
wiley +1 more source
Fístulas arteriovenosas traumáticas agudas
Se presenta casos de Traumatismo simultáneo arterial y venoso de los troncos subclavios y poplíteos. A propósito de ellos se plantea la consideTación de la FAV traumática aguda, como una entida,d definida.
Armando Lanfranconi +3 more
doaj

