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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Autores principales: Şilfeler, Dilek Benk, Karateke, Atilla, Keskin Kurt, Raziye, Aldemir, Özgür, Buğra Nacar, Alper, Baloğlu, Ali
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4269178/
https://www.ncbi.nlm.nih.gov/pubmed/25544917
http://dx.doi.org/10.1155/2014/275710
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author Şilfeler, Dilek Benk
Karateke, Atilla
Keskin Kurt, Raziye
Aldemir, Özgür
Buğra Nacar, Alper
Baloğlu, Ali
author_facet Şilfeler, Dilek Benk
Karateke, Atilla
Keskin Kurt, Raziye
Aldemir, Özgür
Buğra Nacar, Alper
Baloğlu, Ali
author_sort Şilfeler, Dilek Benk
collection PubMed
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.
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spelling pubmed-42691782014-12-28 Malouf Syndrome with Hypergonadotropic Hypogonadism and Cardiomyopathy: Two-Case Report and Literature Review Şilfeler, Dilek Benk Karateke, Atilla Keskin Kurt, Raziye Aldemir, Özgür Buğra Nacar, Alper Baloğlu, Ali Case Rep Obstet Gynecol Case Report 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. Hindawi Publishing Corporation 2014 2014-12-03 /pmc/articles/PMC4269178/ /pubmed/25544917 http://dx.doi.org/10.1155/2014/275710 Text en Copyright © 2014 Dilek Benk Şilfeler et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Şilfeler, Dilek Benk
Karateke, Atilla
Keskin Kurt, Raziye
Aldemir, Özgür
Buğra Nacar, Alper
Baloğlu, Ali
Malouf Syndrome with Hypergonadotropic Hypogonadism and Cardiomyopathy: Two-Case Report and Literature Review
title 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_short 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
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4269178/
https://www.ncbi.nlm.nih.gov/pubmed/25544917
http://dx.doi.org/10.1155/2014/275710
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