Marfan's syndrome, dextrocardia and situs inversus associated with discrete subaortic stenosis and aortic insufficiency in an adult female: Case report

Mustafa Gökçe; Cevdet Erdöl; Sükrü Çelik; Merih Baykan; Hidayet Erdöl; Ahmet Sari; Ali Ahmetoglu

Marfan's syndrome, dextrocardia and situs inversus associated with discrete subaortic stenosis and aortic insufficiency in an adult female: Case report

Mustafa Gökçe
, Cevdet Erdöl^*
, Sükrü Çelik
, Merih Baykan
, Hidayet Erdöl
, Ahmet Sari
, Ali Ahmetoglu

^*Corresponding author for this work

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

2 Scopus citations

Abstract

Marfan's syndrome is an inherited connective tissue defect that affects many organs, especially of the musculoskeletal, ophthalmic and cardiovascular systems, and may be associated with some rare conditions. Here, we report the first known case of Marfan's syndrome, combined with situs inversus totalis with dextrocardia and discrete subaortic stenosis and aortic insufficiency in a 22-year-old woman.

Original language	English
Pages (from-to)	415-417
Number of pages	3
Journal	Journal of Heart Valve Disease
Volume	10
Issue number	3
State	Published - May 2001
Externally published	Yes

ASJC Scopus subject areas

Cardiology and Cardiovascular Medicine

Cite this

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title = "Marfan's syndrome, dextrocardia and situs inversus associated with discrete subaortic stenosis and aortic insufficiency in an adult female: Case report",

abstract = "Marfan's syndrome is an inherited connective tissue defect that affects many organs, especially of the musculoskeletal, ophthalmic and cardiovascular systems, and may be associated with some rare conditions. Here, we report the first known case of Marfan's syndrome, combined with situs inversus totalis with dextrocardia and discrete subaortic stenosis and aortic insufficiency in a 22-year-old woman.",

author = "Mustafa G{\"o}k{\c c}e and Cevdet Erd{\"o}l and S{\"u}kr{\"u} {\c C}elik and Merih Baykan and Hidayet Erd{\"o}l and Ahmet Sari and Ali Ahmetoglu",

year = "2001",

month = may,

language = "English",

volume = "10",

pages = "415--417",

journal = "Journal of Heart Valve Disease",

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TY - JOUR

T1 - Marfan's syndrome, dextrocardia and situs inversus associated with discrete subaortic stenosis and aortic insufficiency in an adult female

T2 - Case report

AU - Gökçe, Mustafa

AU - Erdöl, Cevdet

AU - Çelik, Sükrü

AU - Baykan, Merih

AU - Erdöl, Hidayet

AU - Sari, Ahmet

AU - Ahmetoglu, Ali

PY - 2001/5

Y1 - 2001/5

N2 - Marfan's syndrome is an inherited connective tissue defect that affects many organs, especially of the musculoskeletal, ophthalmic and cardiovascular systems, and may be associated with some rare conditions. Here, we report the first known case of Marfan's syndrome, combined with situs inversus totalis with dextrocardia and discrete subaortic stenosis and aortic insufficiency in a 22-year-old woman.

AB - Marfan's syndrome is an inherited connective tissue defect that affects many organs, especially of the musculoskeletal, ophthalmic and cardiovascular systems, and may be associated with some rare conditions. Here, we report the first known case of Marfan's syndrome, combined with situs inversus totalis with dextrocardia and discrete subaortic stenosis and aortic insufficiency in a 22-year-old woman.

UR - https://www.scopus.com/pages/publications/1642580657

M3 - Article

C2 - 11380111

AN - SCOPUS:1642580657

SN - 0966-8519

VL - 10

SP - 415

EP - 417

JO - Journal of Heart Valve Disease

JF - Journal of Heart Valve Disease

IS - 3

ER -

Marfan's syndrome, dextrocardia and situs inversus associated with discrete subaortic stenosis and aortic insufficiency in an adult female: Case report

Abstract

ASJC Scopus subject areas

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