A complex unit for a complex disease: the HCM-Family Unit

Hypertrophic cardiomyopathy (HCM) is a group of heterogeneous disorders that are most commonly passed on in a heritable manner. It is a relatively rare disease around the globe, but due to increased rates of consanguinity within the Kingdom of Saudi Arabia, we speculate a high incidence of undiagnos...
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Autor*in:	Olga Vriz [verfasserIn] Hani AlSergani [verfasserIn] Ahmed Nahid Elshaer [verfasserIn] Abdullah Shaik [verfasserIn] Ali Hassan Mushtaq [verfasserIn] Michele Lioncino [verfasserIn] Bandar Alamro [verfasserIn] Emanuele Monda [verfasserIn] Martina Caiazza [verfasserIn] Ciro Mauro [verfasserIn] Eduardo Bossone [verfasserIn] Zuhair N. Al-Hassnan [verfasserIn] Dimpna Albert-Brotons [verfasserIn] Giuseppe Limongelli [verfasserIn]

Format:	E-Artikel
Sprache:	Englisch

Erschienen:	2021

Schlagwörter:	Hypertrophic Cardiomyopathy Genetics Hypertrophic Cardiomyopathy Unit

Übergeordnetes Werk:	In: Monaldi Archives for Chest Disease - PAGEPress Publications, 2019, (2021)
Übergeordnetes Werk:	year:2021

Links:	Link aufrufen Link aufrufen Link aufrufen Journal toc Journal toc

DOI / URN:	10.4081/monaldi.2021.2147

Katalog-ID:	DOAJ070318506

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520			\|a Hypertrophic cardiomyopathy (HCM) is a group of heterogeneous disorders that are most commonly passed on in a heritable manner. It is a relatively rare disease around the globe, but due to increased rates of consanguinity within the Kingdom of Saudi Arabia, we speculate a high incidence of undiagnosed cases. The aim of this paper is to elucidate a systematic approach in dealing with HCM patients and since HCM has variable presentation, we have summarized differentials for diagnosis and how different subtypes and genes can have an impact on the clinical picture, management and prognosis. Moreover, we propose a referral multi-disciplinary team HCM-Family Unit in Saudi Arabia and an integrated role in a network between King Faisal Hospital and Inherited and Rare Cardiovascular Disease Unit-Monaldi Hospital, Italy (among the 24 excellence centers of the European Reference Network (ERN) GUARD-Heart). Graphical Abstract
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spelling	10.4081/monaldi.2021.2147 doi (DE-627)DOAJ070318506 (DE-599)DOAJ194b77147698416d9fffec52d9524e46 DE-627 ger DE-627 rakwb eng Olga Vriz verfasserin aut A complex unit for a complex disease: the HCM-Family Unit 2021 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Hypertrophic cardiomyopathy (HCM) is a group of heterogeneous disorders that are most commonly passed on in a heritable manner. It is a relatively rare disease around the globe, but due to increased rates of consanguinity within the Kingdom of Saudi Arabia, we speculate a high incidence of undiagnosed cases. The aim of this paper is to elucidate a systematic approach in dealing with HCM patients and since HCM has variable presentation, we have summarized differentials for diagnosis and how different subtypes and genes can have an impact on the clinical picture, management and prognosis. Moreover, we propose a referral multi-disciplinary team HCM-Family Unit in Saudi Arabia and an integrated role in a network between King Faisal Hospital and Inherited and Rare Cardiovascular Disease Unit-Monaldi Hospital, Italy (among the 24 excellence centers of the European Reference Network (ERN) GUARD-Heart). Graphical Abstract Hypertrophic Cardiomyopathy Genetics Hypertrophic Cardiomyopathy Unit Medicine R Hani AlSergani verfasserin aut Ahmed Nahid Elshaer verfasserin aut Abdullah Shaik verfasserin aut Ali Hassan Mushtaq verfasserin aut Michele Lioncino verfasserin aut Bandar Alamro verfasserin aut Emanuele Monda verfasserin aut Martina Caiazza verfasserin aut Ciro Mauro verfasserin aut Eduardo Bossone verfasserin aut Zuhair N. Al-Hassnan verfasserin aut Dimpna Albert-Brotons verfasserin aut Giuseppe Limongelli verfasserin aut In Monaldi Archives for Chest Disease PAGEPress Publications, 2019 (2021) (DE-627)537441069 (DE-600)2375904-5 25325264 nnns year:2021 https://doi.org/10.4081/monaldi.2021.2147 kostenfrei https://doaj.org/article/194b77147698416d9fffec52d9524e46 kostenfrei https://www.monaldi-archives.org/index.php/macd/article/view/2147 kostenfrei https://doaj.org/toc/1122-0643 Journal toc kostenfrei https://doaj.org/toc/2532-5264 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 2021
allfields_unstemmed	10.4081/monaldi.2021.2147 doi (DE-627)DOAJ070318506 (DE-599)DOAJ194b77147698416d9fffec52d9524e46 DE-627 ger DE-627 rakwb eng Olga Vriz verfasserin aut A complex unit for a complex disease: the HCM-Family Unit 2021 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Hypertrophic cardiomyopathy (HCM) is a group of heterogeneous disorders that are most commonly passed on in a heritable manner. It is a relatively rare disease around the globe, but due to increased rates of consanguinity within the Kingdom of Saudi Arabia, we speculate a high incidence of undiagnosed cases. The aim of this paper is to elucidate a systematic approach in dealing with HCM patients and since HCM has variable presentation, we have summarized differentials for diagnosis and how different subtypes and genes can have an impact on the clinical picture, management and prognosis. Moreover, we propose a referral multi-disciplinary team HCM-Family Unit in Saudi Arabia and an integrated role in a network between King Faisal Hospital and Inherited and Rare Cardiovascular Disease Unit-Monaldi Hospital, Italy (among the 24 excellence centers of the European Reference Network (ERN) GUARD-Heart). Graphical Abstract Hypertrophic Cardiomyopathy Genetics Hypertrophic Cardiomyopathy Unit Medicine R Hani AlSergani verfasserin aut Ahmed Nahid Elshaer verfasserin aut Abdullah Shaik verfasserin aut Ali Hassan Mushtaq verfasserin aut Michele Lioncino verfasserin aut Bandar Alamro verfasserin aut Emanuele Monda verfasserin aut Martina Caiazza verfasserin aut Ciro Mauro verfasserin aut Eduardo Bossone verfasserin aut Zuhair N. Al-Hassnan verfasserin aut Dimpna Albert-Brotons verfasserin aut Giuseppe Limongelli verfasserin aut In Monaldi Archives for Chest Disease PAGEPress Publications, 2019 (2021) (DE-627)537441069 (DE-600)2375904-5 25325264 nnns year:2021 https://doi.org/10.4081/monaldi.2021.2147 kostenfrei https://doaj.org/article/194b77147698416d9fffec52d9524e46 kostenfrei https://www.monaldi-archives.org/index.php/macd/article/view/2147 kostenfrei https://doaj.org/toc/1122-0643 Journal toc kostenfrei https://doaj.org/toc/2532-5264 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 2021
allfieldsGer	10.4081/monaldi.2021.2147 doi (DE-627)DOAJ070318506 (DE-599)DOAJ194b77147698416d9fffec52d9524e46 DE-627 ger DE-627 rakwb eng Olga Vriz verfasserin aut A complex unit for a complex disease: the HCM-Family Unit 2021 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Hypertrophic cardiomyopathy (HCM) is a group of heterogeneous disorders that are most commonly passed on in a heritable manner. It is a relatively rare disease around the globe, but due to increased rates of consanguinity within the Kingdom of Saudi Arabia, we speculate a high incidence of undiagnosed cases. The aim of this paper is to elucidate a systematic approach in dealing with HCM patients and since HCM has variable presentation, we have summarized differentials for diagnosis and how different subtypes and genes can have an impact on the clinical picture, management and prognosis. Moreover, we propose a referral multi-disciplinary team HCM-Family Unit in Saudi Arabia and an integrated role in a network between King Faisal Hospital and Inherited and Rare Cardiovascular Disease Unit-Monaldi Hospital, Italy (among the 24 excellence centers of the European Reference Network (ERN) GUARD-Heart). Graphical Abstract Hypertrophic Cardiomyopathy Genetics Hypertrophic Cardiomyopathy Unit Medicine R Hani AlSergani verfasserin aut Ahmed Nahid Elshaer verfasserin aut Abdullah Shaik verfasserin aut Ali Hassan Mushtaq verfasserin aut Michele Lioncino verfasserin aut Bandar Alamro verfasserin aut Emanuele Monda verfasserin aut Martina Caiazza verfasserin aut Ciro Mauro verfasserin aut Eduardo Bossone verfasserin aut Zuhair N. Al-Hassnan verfasserin aut Dimpna Albert-Brotons verfasserin aut Giuseppe Limongelli verfasserin aut In Monaldi Archives for Chest Disease PAGEPress Publications, 2019 (2021) (DE-627)537441069 (DE-600)2375904-5 25325264 nnns year:2021 https://doi.org/10.4081/monaldi.2021.2147 kostenfrei https://doaj.org/article/194b77147698416d9fffec52d9524e46 kostenfrei https://www.monaldi-archives.org/index.php/macd/article/view/2147 kostenfrei https://doaj.org/toc/1122-0643 Journal toc kostenfrei https://doaj.org/toc/2532-5264 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 2021
allfieldsSound	10.4081/monaldi.2021.2147 doi (DE-627)DOAJ070318506 (DE-599)DOAJ194b77147698416d9fffec52d9524e46 DE-627 ger DE-627 rakwb eng Olga Vriz verfasserin aut A complex unit for a complex disease: the HCM-Family Unit 2021 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Hypertrophic cardiomyopathy (HCM) is a group of heterogeneous disorders that are most commonly passed on in a heritable manner. It is a relatively rare disease around the globe, but due to increased rates of consanguinity within the Kingdom of Saudi Arabia, we speculate a high incidence of undiagnosed cases. The aim of this paper is to elucidate a systematic approach in dealing with HCM patients and since HCM has variable presentation, we have summarized differentials for diagnosis and how different subtypes and genes can have an impact on the clinical picture, management and prognosis. Moreover, we propose a referral multi-disciplinary team HCM-Family Unit in Saudi Arabia and an integrated role in a network between King Faisal Hospital and Inherited and Rare Cardiovascular Disease Unit-Monaldi Hospital, Italy (among the 24 excellence centers of the European Reference Network (ERN) GUARD-Heart). Graphical Abstract Hypertrophic Cardiomyopathy Genetics Hypertrophic Cardiomyopathy Unit Medicine R Hani AlSergani verfasserin aut Ahmed Nahid Elshaer verfasserin aut Abdullah Shaik verfasserin aut Ali Hassan Mushtaq verfasserin aut Michele Lioncino verfasserin aut Bandar Alamro verfasserin aut Emanuele Monda verfasserin aut Martina Caiazza verfasserin aut Ciro Mauro verfasserin aut Eduardo Bossone verfasserin aut Zuhair N. Al-Hassnan verfasserin aut Dimpna Albert-Brotons verfasserin aut Giuseppe Limongelli verfasserin aut In Monaldi Archives for Chest Disease PAGEPress Publications, 2019 (2021) (DE-627)537441069 (DE-600)2375904-5 25325264 nnns year:2021 https://doi.org/10.4081/monaldi.2021.2147 kostenfrei https://doaj.org/article/194b77147698416d9fffec52d9524e46 kostenfrei https://www.monaldi-archives.org/index.php/macd/article/view/2147 kostenfrei https://doaj.org/toc/1122-0643 Journal toc kostenfrei https://doaj.org/toc/2532-5264 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 2021
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authorswithroles_txt_mv	Olga Vriz @@aut@@ Hani AlSergani @@aut@@ Ahmed Nahid Elshaer @@aut@@ Abdullah Shaik @@aut@@ Ali Hassan Mushtaq @@aut@@ Michele Lioncino @@aut@@ Bandar Alamro @@aut@@ Emanuele Monda @@aut@@ Martina Caiazza @@aut@@ Ciro Mauro @@aut@@ Eduardo Bossone @@aut@@ Zuhair N. Al-Hassnan @@aut@@ Dimpna Albert-Brotons @@aut@@ Giuseppe Limongelli @@aut@@
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author	Olga Vriz
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topic_title	A complex unit for a complex disease: the HCM-Family Unit Hypertrophic Cardiomyopathy Genetics Hypertrophic Cardiomyopathy Unit
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title	A complex unit for a complex disease: the HCM-Family Unit
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title_full	A complex unit for a complex disease: the HCM-Family Unit
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author_browse	Olga Vriz Hani AlSergani Ahmed Nahid Elshaer Abdullah Shaik Ali Hassan Mushtaq Michele Lioncino Bandar Alamro Emanuele Monda Martina Caiazza Ciro Mauro Eduardo Bossone Zuhair N. Al-Hassnan Dimpna Albert-Brotons Giuseppe Limongelli
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title_sort	complex unit for a complex disease: the hcm-family unit
title_auth	A complex unit for a complex disease: the HCM-Family Unit
abstract	Hypertrophic cardiomyopathy (HCM) is a group of heterogeneous disorders that are most commonly passed on in a heritable manner. It is a relatively rare disease around the globe, but due to increased rates of consanguinity within the Kingdom of Saudi Arabia, we speculate a high incidence of undiagnosed cases. The aim of this paper is to elucidate a systematic approach in dealing with HCM patients and since HCM has variable presentation, we have summarized differentials for diagnosis and how different subtypes and genes can have an impact on the clinical picture, management and prognosis. Moreover, we propose a referral multi-disciplinary team HCM-Family Unit in Saudi Arabia and an integrated role in a network between King Faisal Hospital and Inherited and Rare Cardiovascular Disease Unit-Monaldi Hospital, Italy (among the 24 excellence centers of the European Reference Network (ERN) GUARD-Heart). Graphical Abstract
abstractGer	Hypertrophic cardiomyopathy (HCM) is a group of heterogeneous disorders that are most commonly passed on in a heritable manner. It is a relatively rare disease around the globe, but due to increased rates of consanguinity within the Kingdom of Saudi Arabia, we speculate a high incidence of undiagnosed cases. The aim of this paper is to elucidate a systematic approach in dealing with HCM patients and since HCM has variable presentation, we have summarized differentials for diagnosis and how different subtypes and genes can have an impact on the clinical picture, management and prognosis. Moreover, we propose a referral multi-disciplinary team HCM-Family Unit in Saudi Arabia and an integrated role in a network between King Faisal Hospital and Inherited and Rare Cardiovascular Disease Unit-Monaldi Hospital, Italy (among the 24 excellence centers of the European Reference Network (ERN) GUARD-Heart). Graphical Abstract
abstract_unstemmed	Hypertrophic cardiomyopathy (HCM) is a group of heterogeneous disorders that are most commonly passed on in a heritable manner. It is a relatively rare disease around the globe, but due to increased rates of consanguinity within the Kingdom of Saudi Arabia, we speculate a high incidence of undiagnosed cases. The aim of this paper is to elucidate a systematic approach in dealing with HCM patients and since HCM has variable presentation, we have summarized differentials for diagnosis and how different subtypes and genes can have an impact on the clinical picture, management and prognosis. Moreover, we propose a referral multi-disciplinary team HCM-Family Unit in Saudi Arabia and an integrated role in a network between King Faisal Hospital and Inherited and Rare Cardiovascular Disease Unit-Monaldi Hospital, Italy (among the 24 excellence centers of the European Reference Network (ERN) GUARD-Heart). Graphical Abstract
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title_short	A complex unit for a complex disease: the HCM-Family Unit
url	https://doi.org/10.4081/monaldi.2021.2147 https://doaj.org/article/194b77147698416d9fffec52d9524e46 https://www.monaldi-archives.org/index.php/macd/article/view/2147 https://doaj.org/toc/1122-0643 https://doaj.org/toc/2532-5264
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author2	Hani AlSergani Ahmed Nahid Elshaer Abdullah Shaik Ali Hassan Mushtaq Michele Lioncino Bandar Alamro Emanuele Monda Martina Caiazza Ciro Mauro Eduardo Bossone Zuhair N. Al-Hassnan Dimpna Albert-Brotons Giuseppe Limongelli
author2Str	Hani AlSergani Ahmed Nahid Elshaer Abdullah Shaik Ali Hassan Mushtaq Michele Lioncino Bandar Alamro Emanuele Monda Martina Caiazza Ciro Mauro Eduardo Bossone Zuhair N. Al-Hassnan Dimpna Albert-Brotons Giuseppe Limongelli
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up_date	2024-07-03T14:09:27.594Z
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It is a relatively rare disease around the globe, but due to increased rates of consanguinity within the Kingdom of Saudi Arabia, we speculate a high incidence of undiagnosed cases. The aim of this paper is to elucidate a systematic approach in dealing with HCM patients and since HCM has variable presentation, we have summarized differentials for diagnosis and how different subtypes and genes can have an impact on the clinical picture, management and prognosis. Moreover, we propose a referral multi-disciplinary team HCM-Family Unit in Saudi Arabia and an integrated role in a network between King Faisal Hospital and Inherited and Rare Cardiovascular Disease Unit-Monaldi Hospital, Italy (among the 24 excellence centers of the European Reference Network (ERN) GUARD-Heart). 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A complex unit for a complex disease: the HCM-Family Unit

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