Literature DB >> 28421916

Mucopolysaccharidoses Causing Valvular Heart Disease: Report and Review of Surgical Management.

Carlos O Encarnacion1, Dustin Hang1, Michael Earing2, Michael E Mitchell3,4.   

Abstract

Mucopolysaccharidosis type I is a genetic disorder with impaired glycosaminoglycan degradation. Cardiac pathologic involvement in this subset of patients is predominantly valvular heart disease. Valvular heart disease seen in these patients will most likely require surgical intervention in their lifetime. Only a limited amount of reports are dedicated to the cardiac surgical management of mucopolysaccharidoses. We present the case of a 32-year-old female with Hurler-Scheie syndrome who required multiple valve replacements due to progression of valvular dysfunction and decline in the quality of life. Multidisciplinary evaluation and discussion early are crucial for quality of life optimization in this cohort of patients.

Entities:  

Keywords:  adult congenital heart disease; congenital heart disease; congenital heart surgery; mitral valve replacement

Mesh:

Year:  2017        PMID: 28421916     DOI: 10.1177/2150135117690105

Source DB:  PubMed          Journal:  World J Pediatr Congenit Heart Surg        ISSN: 2150-1351


  4 in total

Review 1.  Surgical Management of Valvular Heart Disease in Mucopolysaccharidoses: A Review of Literature.

Authors:  Barbara A Rosser; Calvin Chan; Andreas Hoschtitzky
Journal:  Biomedicines       Date:  2022-02-04

Review 2.  Pre-operative Considerations in Adult Mucopolysaccharidosis Patients Planned for Cardiac Intervention.

Authors:  Benjamin Cross; Karolina M Stepien; Chaitanya Gadepalli; Ahmed Kharabish; Peter Woolfson; Govind Tol; Petra Jenkins
Journal:  Front Cardiovasc Med       Date:  2022-04-04

3.  Heart valve disease in Hurler-Scheie syndrome.

Authors:  María Del Carmen García Del Rey; Javier Castrodeza; Ángel Pinto; Maria Ángeles Espinosa Castro; Cecilia Muñoz Delgado; Francisco Fernández-Avilés
Journal:  Cardiol J       Date:  2022-07-12       Impact factor: 3.487

4.  Diagnosis of Mucopolysaccharidosis Based on History and Clinical Features: Evidence from the Bajio Region of Mexico.

Authors:  Douglas Colmenares-Bonilla; Christian Colin-Gonzalez; Alejandra Gonzalez-Segoviano; Enrique Esquivel Garcia; Ma Martha Vela-Huerta; Fanny Guadalupe Lopez-Gomez
Journal:  Cureus       Date:  2018-11-20
  4 in total

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