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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Main Authors: Dilek Benk Şilfeler, Atilla Karateke, Raziye Keskin Kurt, Özgür Aldemir, Alper Buğra Nacar, Ali Baloğlu
Format: Article
Language:English
Published: Hindawi Limited 2014-01-01
Series:Case Reports in Obstetrics and Gynecology
Online Access:http://dx.doi.org/10.1155/2014/275710
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spelling 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
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