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Uhl's Anomaly in Adulthood.
Mohamed, Omar A M; El-Dardeery, Marwa; Zayed, Kareem; Mosaad, Eleia; Abdulwahhab, Muhammad M; Romeih, Soha.
Afiliación
  • Mohamed OAM; Department of Critical Care Medicine, Magdi Yacoub Heart Foundation, Aswan Heart Center, Aswan, Egypt.
  • El-Dardeery M; Department of Adult Congenital Heart Disease, Magdi Yacoub Heart Foundation, Aswan Heart Center, Aswan, Egypt.
  • Zayed K; Department of Cardiac Surgery, Magdi Yacoub Heart Foundation, Aswan Heart Center, Aswan, Egypt.
  • Mosaad E; Department of Critical Care Medicine, Magdi Yacoub Heart Foundation, Aswan Heart Center, Aswan, Egypt.
  • Abdulwahhab MM; Department of Critical Care Medicine, Magdi Yacoub Heart Foundation, Aswan Heart Center, Aswan, Egypt.
  • Romeih S; Department of Adult Congenital Heart Disease, Magdi Yacoub Heart Foundation, Aswan Heart Center, Aswan, Egypt.
World J Pediatr Congenit Heart Surg ; 15(4): 523-525, 2024 Jul.
Article en En | MEDLINE | ID: mdl-38693789
ABSTRACT
Uhl's anomaly is a rare congenital syndrome characterized by the absence of right ventricular myocardium. The widely accepted pathological mechanism is intrauterine myocardial apoptosis. Uhl's syndrome carries a poor prognosis. In rare situations, patients with Uhl's anomaly reach adulthood. We will present a case of a 29-year-old patient with Uhl's syndrome treated at our center, highlighting the diagnostic, surgical, and postoperative challenges in management.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Cardiopatías Congénitas Límite: Adult / Female / Humans / Male Idioma: En Revista: World J Pediatr Congenit Heart Surg Año: 2024 Tipo del documento: Article País de afiliación: Egipto Pais de publicación: Estados Unidos
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Cardiopatías Congénitas Límite: Adult / Female / Humans / Male Idioma: En Revista: World J Pediatr Congenit Heart Surg Año: 2024 Tipo del documento: Article País de afiliación: Egipto Pais de publicación: Estados Unidos