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Revisión bibliográfica y presentación de un caso: síndrome de marfán
(Universidad de Cuenca, 2016-05)
Marfan syndrome is a rare disease, caused
by a genetic mutation of fibrillin-1, essential
for the synthesis of connective tissue elastic
fibers. It is characterized by a high penetrance
and a marked phenotypic ...
Estrategias terapéuticas de aneurisma abdominal en sindrome de Marfan a propósito de un caso
(Universidad de Cuenca. Facultad de Ciencias Médicas, 2001-12)
It is presented a case of a patient who attends outpatient
consultation at the Vicente Corral Moscoso
hospital with a diagnosis of abdominal aortic
aneurysm which was identified through tomography.
Besides, the patient ...