A study of a family with inherited disease of cardiac and skeletal muscle - Part I. Clinical, electrocardiographic, echocardiographic, Haemodynamic, electrophysiological and electron microscopic studies
A family consisting of parents and their 6 sons were investigated to elucidate the relationship between a hypertrophic cardiomyopathy, musculoskeletal abnormalities and mental subnormality.
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| Veröffentlicht in: | South African medical journal 1981-03, Vol.59 (11), p.363-373 |
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| container_end_page | 373 |
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| container_issue | 11 |
| container_start_page | 363 |
| container_title | South African medical journal |
| container_volume | 59 |
| creator | Przybojewski, J.Z., Hoffman, H., de Graaf, A.S., van der Walt, J.J., Tiedt, F.A.C., O'Kennedy, A., Torrington, M., Lochner, A. & Hewlett, R. |
| description | A family consisting of parents and their 6 sons were investigated to elucidate the relationship between a hypertrophic cardiomyopathy, musculoskeletal abnormalities and mental subnormality. |
| format | Article |
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Clinical, electrocardiographic, echocardiographic, Haemodynamic, electrophysiological and electron microscopic studies</title><title>South African medical journal</title><addtitle>S Afr Med J</addtitle><description>A family consisting of parents and their 6 sons were investigated to elucidate the relationship between a hypertrophic cardiomyopathy, musculoskeletal abnormalities and mental subnormality.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Anthropometry</subject><subject>Cardiology</subject><subject>Cardiomyopathy, Hypertrophic - genetics</subject><subject>Diagnosis</subject><subject>ECG</subject><subject>Echocardiography</subject><subject>Electrocardiography</subject><subject>Electroencephalography</subject><subject>Electromyography</subject><subject>Family study</subject><subject>Female</subject><subject>Haemodynamics</subject><subject>Heart - physiopathology</subject><subject>Hemodynamics</subject><subject>Histocompatibility Testing</subject><subject>Histology</subject><subject>HLA Antigens - analysis</subject><subject>Humans</subject><subject>Hypertrophic cardiomyopathy</subject><subject>Intellectual Disability - genetics</subject><subject>Male</subject><subject>Mental subnormality</subject><subject>Microscopy, Electron</subject><subject>Mitochondria, Muscle - pathology</subject><subject>Muscles - pathology</subject><subject>Musculoskeletal abnormality</subject><subject>Myocardium - pathology</subject><subject>Myofibrils - ultrastructure</subject><subject>Neurology</subject><subject>Neuromuscular Diseases - genetics</subject><issn>0256-9574</issn><issn>2078-5135</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1981</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkc1q3DAQx01JSbdpH6GgU09xkWRrJR2XJemmBNJD7mYsjWO1suVKNsGv2KeKdrPkkNMw8__N94diw6lUpWCVuCg2lIttqYWsPxWfU_pDsy_09rK4lExXlag3xf8dSfNiVxI6AqSDwfmVPLu5J27sMboZLbEuISQ8IgaidWAIjJakv-hxBk-GJRmPpCS_Ic7k7gfZezc6A_6aZMLMMZzSwlOEqXcmR03_PnQAHIJdxzyAeUub-jW54MPTsdip51kYScZiSCZMzpwWcJi-FB878Am_nu1V8Xh787g_lPcPP-_2u_ty0kyWtZLMKl1bBW2nwDLdcWlaUPlURtWKylpbqlqknbACoTK63YqtRclqzlhXXRXfX8tOMfxbMM3N4JJB72HEsKRGCiE41zSD387g0g5omym6AeLanG-f9fJVT9C6EecmAWa0YVRw2ux-7Y6fPD6yYRXnsnoBY0mTPw</recordid><startdate>19810314</startdate><enddate>19810314</enddate><creator>Przybojewski, J.Z., Hoffman, H., de Graaf, A.S., van der Walt, J.J., Tiedt, F.A.C., O'Kennedy, A., Torrington, M., Lochner, A. & Hewlett, R.</creator><general>Health and Medical Publishing Group (HMPG)</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>19810314</creationdate><title>A study of a family with inherited disease of cardiac and skeletal muscle - Part I. Clinical, electrocardiographic, echocardiographic, Haemodynamic, electrophysiological and electron microscopic studies</title><author>Przybojewski, J.Z., Hoffman, H., de Graaf, A.S., van der Walt, J.J., Tiedt, F.A.C., O'Kennedy, A., Torrington, M., Lochner, A. & Hewlett, R.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p917-4871d894d8abf8ad19f27cba8256c8480749d08be0f5d5ea3c9b656de714211f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1981</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Anthropometry</topic><topic>Cardiology</topic><topic>Cardiomyopathy, Hypertrophic - genetics</topic><topic>Diagnosis</topic><topic>ECG</topic><topic>Echocardiography</topic><topic>Electrocardiography</topic><topic>Electroencephalography</topic><topic>Electromyography</topic><topic>Family study</topic><topic>Female</topic><topic>Haemodynamics</topic><topic>Heart - physiopathology</topic><topic>Hemodynamics</topic><topic>Histocompatibility Testing</topic><topic>Histology</topic><topic>HLA Antigens - analysis</topic><topic>Humans</topic><topic>Hypertrophic cardiomyopathy</topic><topic>Intellectual Disability - genetics</topic><topic>Male</topic><topic>Mental subnormality</topic><topic>Microscopy, Electron</topic><topic>Mitochondria, Muscle - pathology</topic><topic>Muscles - pathology</topic><topic>Musculoskeletal abnormality</topic><topic>Myocardium - pathology</topic><topic>Myofibrils - ultrastructure</topic><topic>Neurology</topic><topic>Neuromuscular Diseases - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Przybojewski, J.Z., Hoffman, H., de Graaf, A.S., van der Walt, J.J., Tiedt, F.A.C., O'Kennedy, A., Torrington, M., Lochner, A. & Hewlett, R.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>South African medical journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Przybojewski, J.Z., Hoffman, H., de Graaf, A.S., van der Walt, J.J., Tiedt, F.A.C., O'Kennedy, A., Torrington, M., Lochner, A. & Hewlett, R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A study of a family with inherited disease of cardiac and skeletal muscle - Part I. 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| identifier | ISSN: 0256-9574 |
| ispartof | South African medical journal, 1981-03, Vol.59 (11), p.363-373 |
| issn | 0256-9574 2078-5135 |
| language | eng |
| recordid | cdi_proquest_miscellaneous_75552290 |
| source | Sabinet African Journals Open Access Collection |
| subjects | Adolescent Adult Anthropometry Cardiology Cardiomyopathy, Hypertrophic - genetics Diagnosis ECG Echocardiography Electrocardiography Electroencephalography Electromyography Family study Female Haemodynamics Heart - physiopathology Hemodynamics Histocompatibility Testing Histology HLA Antigens - analysis Humans Hypertrophic cardiomyopathy Intellectual Disability - genetics Male Mental subnormality Microscopy, Electron Mitochondria, Muscle - pathology Muscles - pathology Musculoskeletal abnormality Myocardium - pathology Myofibrils - ultrastructure Neurology Neuromuscular Diseases - genetics |
| title | A study of a family with inherited disease of cardiac and skeletal muscle - Part I. Clinical, electrocardiographic, echocardiographic, Haemodynamic, electrophysiological and electron microscopic studies |
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