Eisenmenger Syndrome in Congenital Heart Disease with Clinical Features of Differential (Fingers and Toes) Clubbing and Cyanosis

Mateo Porres-Aguilar; Carlos E. Rodriguez-Castro; Mateo Porres-Munoz; Cesar A. Siska; Jose L. Aguirre; Alma Santiago-Balandran; Aamer Abbas; Oscar C. Munoz; Debabrata Mukherjee

doi:10.12659/MSCR.892953

Eisenmenger Syndrome in Congenital Heart Disease with Clinical Features of Differential (Fingers and Toes) Clubbing and Cyanosis

Mateo Porres-Aguilar
, Carlos E. Rodriguez-Castro
, Mateo Porres-Munoz
, Cesar A. Siska
, Jose L. Aguirre
, Alma Santiago-Balandran
, Aamer Abbas
, Oscar C. Munoz
, Debabrata Mukherjee

Texas Tech University Health Sciences Center
Autonomous University of Tamaulipas
Universidad Autonoma de Ciudad Juarez
Department of Emergency Medicine, Hospital General de Ciudad Constitucion, Cuidad Constitucion, Mexico
Department of Cardiovascular Diseases and Invasive Cardiology, Del Sol Medical Center, El Paso, TX, USA

Research output: Contribution to journal › Article › peer-review

Original language	American English
Journal	Medical Science Case Reports
Volume	1
DOIs	https://doi.org/10.12659/MSCR.892953
State	Published - Nov 29 2014
Externally published	Yes

Disciplines

Medicine and Health Sciences
Cardiology
Surgery
Internal Medicine

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10.12659/MSCR.892953License: Unspecified

Cite this

@article{95a4df58b95a48aaa3ceb6ce577a2dfe,

title = "Eisenmenger Syndrome in Congenital Heart Disease with Clinical Features of Differential (Fingers and Toes) Clubbing and Cyanosis",

author = "Mateo Porres-Aguilar and Rodriguez-Castro, \{Carlos E.\} and Mateo Porres-Munoz and Siska, \{Cesar A.\} and Aguirre, \{Jose L.\} and Alma Santiago-Balandran and Aamer Abbas and Munoz, \{Oscar C.\} and Debabrata Mukherjee",

note = "b]Background[/b] Eisenmenger syndrome represents the most advanced form of pulmonary arterial hypertension (PAH) associated with congenital heart disease. Although patients with Eisenmenger syndrome frequently survive in to their third or fourth decade of life, the severity and progression of symptoms of the disease, including cardiac dysrhythmias, prothrombotic and bleeding diathesis, and right ventricular failure represent frequent late complications and causes of sudden death.",

year = "2014",

month = nov,

day = "29",

doi = "10.12659/MSCR.892953",

language = "American English",

volume = "1",

journal = "Medical Science Case Reports",

}

TY - JOUR

T1 - Eisenmenger Syndrome in Congenital Heart Disease with Clinical Features of Differential (Fingers and Toes) Clubbing and Cyanosis

AU - Porres-Aguilar, Mateo

AU - Rodriguez-Castro, Carlos E.

AU - Porres-Munoz, Mateo

AU - Siska, Cesar A.

AU - Aguirre, Jose L.

AU - Santiago-Balandran, Alma

AU - Abbas, Aamer

AU - Munoz, Oscar C.

AU - Mukherjee, Debabrata

N1 - b]Background[/b] Eisenmenger syndrome represents the most advanced form of pulmonary arterial hypertension (PAH) associated with congenital heart disease. Although patients with Eisenmenger syndrome frequently survive in to their third or fourth decade of life, the severity and progression of symptoms of the disease, including cardiac dysrhythmias, prothrombotic and bleeding diathesis, and right ventricular failure represent frequent late complications and causes of sudden death.

PY - 2014/11/29

Y1 - 2014/11/29

UR - https://www.medscicaserep.com/abstract/index/idArt/892953

U2 - 10.12659/MSCR.892953

DO - 10.12659/MSCR.892953

M3 - Article

VL - 1

JO - Medical Science Case Reports

JF - Medical Science Case Reports

ER -

Eisenmenger Syndrome in Congenital Heart Disease with Clinical Features of Differential (Fingers and Toes) Clubbing and Cyanosis

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