Ebsteins anomaly of the tricuspid valve pathophysiology

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor-In-Chief: Cafer Zorkun, M.D., Ph.D. [2]; Claudia P. Hochberg, M.D. [3];Priyamvada Singh, MBBS [4],Associate Editor(s)-in-Chief: Maneesha Nandimandalam, M.B.B.S.[5]

Overview

The pathophysiology of Ebstein's anomaly depends on the morphology of tricuspid valve and the right ventricle. The annulus of the valve is in normal position. The valve leaflets however, are to a varying degree attached to the walls and septum of the right ventricle. There is subsequent atrialization of a portion of the morphologic right ventricle (which is then contiguous with the right atrium). This causes the right atrium to be large and the anatomic right ventricle to be small in size. 50% of cases involve an atrial shunt (either a PFO or an ASD). Mutations in MYH7, which a sarcomere gene encoding the cardiac beta-myosin heavy chain have been linked in the occurence of familial Ebstein anomaly. Commonly associated conditions include Aortic coarctation, Cleft anterior leaflet of the mitral valve, Coarctation of the aorta, corrected transposition of the great arteries, Hypoplastic pulmonary arteries, Left ventricular outflow obstruction etc.

Pathophysiology

  1. Failure of TV(tricuspid valve) leaflet delamination
  2. Apical descent of the functional tricuspid orifice
  3. Right ventricular dilation and “atrialization”
  4. Anterior leaflet abnormal fenestrations and tethering
  5. Right atrioventricular junction dilation

Source: National Library Of Medicine.


Tricuspid Valve

Right Ventricle

The right ventricle changes secondary to the malformed tricuspid valves. The right ventricle can be divided into two parts by the malformed valve:

Genetics

Associated Conditions

Commonly associated conditions include:[7][8][9][10]

Listed below are the other associated conditions:


References

  1. Kloesel B, DiNardo JA, Body SC (September 2016). "Cardiac Embryology and Molecular Mechanisms of Congenital Heart Disease: A Primer for Anesthesiologists". Anesth. Analg. 123 (3): 551–69. doi:10.1213/ANE.0000000000001451. PMC 4996372. PMID 27541719.
  2. Postma AV, van Engelen K, van de Meerakker J, Rahman T, Probst S, Baars MJ, Bauer U, Pickardt T, Sperling SR, Berger F, Moorman AF, Mulder BJ, Thierfelder L, Keavney B, Goodship J, Klaassen S (February 2011). "Mutations in the sarcomere gene MYH7 in Ebstein anomaly". Circ Cardiovasc Genet. 4 (1): 43–50. doi:10.1161/CIRCGENETICS.110.957985. PMID 21127202.
  3. Bettinelli AL, Mulder TJ, Funke BH, Lafferty KA, Longo SA, Niyazov DM (December 2013). "Familial ebstein anomaly, left ventricular hypertrabeculation, and ventricular septal defect associated with a MYH7 mutation". Am. J. Med. Genet. A. 161A (12): 3187–90. doi:10.1002/ajmg.a.36182. PMID 23956225.
  4. Holst KA, Connolly HM, Dearani JA (2019). "Ebstein's Anomaly". Methodist Debakey Cardiovasc J. 15 (2): 138–144. doi:10.14797/mdcj-15-2-138. PMC 6668741 Check |pmc= value (help). PMID 31384377.
  5. Klaassen S, Probst S, Oechslin E, Gerull B, Krings G, Schuler P, Greutmann M, Hürlimann D, Yegitbasi M, Pons L, Gramlich M, Drenckhahn JD, Heuser A, Berger F, Jenni R, Thierfelder L (June 2008). "Mutations in sarcomere protein genes in left ventricular noncompaction". Circulation. 117 (22): 2893–901. doi:10.1161/CIRCULATIONAHA.107.746164. PMID 18506004.
  6. Pierpont ME, Brueckner M, Chung WK, Garg V, Lacro RV, McGuire AL, Mital S, Priest JR, Pu WT, Roberts A, Ware SM, Gelb BD, Russell MW (November 2018). "Genetic Basis for Congenital Heart Disease: Revisited: A Scientific Statement From the American Heart Association". Circulation. 138 (21): e653–e711. doi:10.1161/CIR.0000000000000606. PMC 6555769 Check |pmc= value (help). PMID 30571578.
  7. Siehr SL, Punn R, Priest JR, Lowenthal A (January 2014). "Ebstein anomaly and Trisomy 21: A rare association". Ann Pediatr Cardiol. 7 (1): 67–9. doi:10.4103/0974-2069.126569. PMC 3959069. PMID 24701093.
  8. Davido A, Maarek M, Jullien JL, Corone P (May 1985). "[Ebstein's disease associated with Fallot's tetralogy. Apropos of a familial case, review of the literature, embryologic and genetic implications]". Arch Mal Coeur Vaiss (in French). 78 (5): 752–6. PMID 3925918.
  9. van Trier DC, Feenstra I, Bot P, de Leeuw N, Draaisma JM (August 2013). "Cardiac anomalies in individuals with the 18q deletion syndrome; report of a child with Ebstein anomaly and review of the literature". Eur J Med Genet. 56 (8): 426–31. doi:10.1016/j.ejmg.2013.05.002. PMID 23707655.
  10. Vermeer AM, van Engelen K, Postma AV, Baars MJ, Christiaans I, De Haij S, Klaassen S, Mulder BJ, Keavney B (August 2013). "Ebstein anomaly associated with left ventricular noncompaction: an autosomal dominant condition that can be caused by mutations in MYH7". Am J Med Genet C Semin Med Genet. 163C (3): 178–84. doi:10.1002/ajmg.c.31365. PMID 23794396.

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