Malouf Syndrome with Hypergonadotropic Hypogonadism and Cardiomyopathy: Two-Case Report and Literature Review
Malouf syndrome is a very rarely encountered syndrome which was first diagnosed in 1985 upon the examination of two sisters, with findings of hypergonadotropic hypogonadism, dilated cardiomyopathy, blepharoptosis, and broad nasal base. Later on, Narahara diagnosed another sporadic case with the same...
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Hindawi Limited
2014-01-01
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Series: | Case Reports in Obstetrics and Gynecology |
Online Access: | http://dx.doi.org/10.1155/2014/275710 |
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doaj-a451151a03984bcf8a62c6d4a96c8f0b2020-11-24T22:46:31ZengHindawi LimitedCase Reports in Obstetrics and Gynecology2090-66842090-66922014-01-01201410.1155/2014/275710275710Malouf Syndrome with Hypergonadotropic Hypogonadism and Cardiomyopathy: Two-Case Report and Literature ReviewDilek Benk Şilfeler0Atilla Karateke1Raziye Keskin Kurt2Özgür Aldemir3Alper Buğra Nacar4Ali Baloğlu5Department of Obstetrics and Gynecology, Mustafa Kemal University Medical School, Hatay, TurkeyClinics of Obstetrics and Gynecology, Hatay Antakya Maternity Hospital, Hatay, TurkeyDepartment of Obstetrics and Gynecology, Mustafa Kemal University Medical School, Hatay, TurkeyDepartment of Genetics, Mustafa Kemal University Medical School, Hatay, TurkeyDepartment of Cardiology, Mustafa Kemal University Medical School, Hatay, TurkeyDepartment of Obstetrics and Gynecology, Mustafa Kemal University Medical School, Hatay, TurkeyMalouf syndrome is a very rarely encountered syndrome which was first diagnosed in 1985 upon the examination of two sisters, with findings of hypergonadotropic hypogonadism, dilated cardiomyopathy, blepharoptosis, and broad nasal base. Later on, Narahara diagnosed another sporadic case with the same findings. A survey of relevant literature leads us to three women cases in total. Here we present two cases of Malouf syndrome and literature review.http://dx.doi.org/10.1155/2014/275710 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Dilek Benk Şilfeler Atilla Karateke Raziye Keskin Kurt Özgür Aldemir Alper Buğra Nacar Ali Baloğlu |
spellingShingle |
Dilek Benk Şilfeler Atilla Karateke Raziye Keskin Kurt Özgür Aldemir Alper Buğra Nacar Ali Baloğlu Malouf Syndrome with Hypergonadotropic Hypogonadism and Cardiomyopathy: Two-Case Report and Literature Review Case Reports in Obstetrics and Gynecology |
author_facet |
Dilek Benk Şilfeler Atilla Karateke Raziye Keskin Kurt Özgür Aldemir Alper Buğra Nacar Ali Baloğlu |
author_sort |
Dilek Benk Şilfeler |
title |
Malouf Syndrome with Hypergonadotropic Hypogonadism and Cardiomyopathy: Two-Case Report and Literature Review |
title_short |
Malouf Syndrome with Hypergonadotropic Hypogonadism and Cardiomyopathy: Two-Case Report and Literature Review |
title_full |
Malouf Syndrome with Hypergonadotropic Hypogonadism and Cardiomyopathy: Two-Case Report and Literature Review |
title_fullStr |
Malouf Syndrome with Hypergonadotropic Hypogonadism and Cardiomyopathy: Two-Case Report and Literature Review |
title_full_unstemmed |
Malouf Syndrome with Hypergonadotropic Hypogonadism and Cardiomyopathy: Two-Case Report and Literature Review |
title_sort |
malouf syndrome with hypergonadotropic hypogonadism and cardiomyopathy: two-case report and literature review |
publisher |
Hindawi Limited |
series |
Case Reports in Obstetrics and Gynecology |
issn |
2090-6684 2090-6692 |
publishDate |
2014-01-01 |
description |
Malouf syndrome is a very rarely encountered syndrome which was first diagnosed in 1985 upon the examination of two sisters, with findings of hypergonadotropic hypogonadism, dilated cardiomyopathy, blepharoptosis, and broad nasal base. Later on, Narahara diagnosed another sporadic case with the same findings. A survey of relevant literature leads us to three women cases in total. Here we present two cases of Malouf syndrome and literature review. |
url |
http://dx.doi.org/10.1155/2014/275710 |
work_keys_str_mv |
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