Cardiomegaly causes: Difference between revisions
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| '''Genetic''' | | '''Genetic''' | ||
|bgcolor="Beige"| [[1p36 deletion syndrome]], [[Alstrom syndrome]], [[Barth syndrome]], [[Becker muscular dystrophy]], [[Beckwith–Wiedemann syndrome]], [[cardiofaciocutaneous syndrome]], [[carnitine palmitoyl transferase deficiency]], [[congenital generalized lipodystrophy]], [[Costello syndrome]], [[Danon disease]], [[Desmin-related myofibrillar myopathy]], [[Duchenne muscular dystrophy]], [[Emery-Dreifuss muscular dystrophy, X-linked]], [[Fabry disease]], [[hypertrophic cardiomyopathy|familial hypertrophic cardiomyopathy]], [[friedreich ataxia]], [[fucosidosis]], [[Gaucher disease]], [[glycogenosis type 2]], [[glycogenosis type 2b]], [[hemochromatosis]], [[hereditary spherocytosis]], [[Hunter syndrome]], [[hypertrichotic osteochondrodysplasia]], [[infantile sialic acid storage disorder]], [[Isobutyryl-CoA dehydrogenase deficiency]], [[Laing distal myopathy]], [[long-chain acyl-CoA dehydrogenase deficiency]], [[Malonyl-CoA decarboxylase deficiency]], [[McLeod neuroacanthocytosis syndrome]], [[MELAS]], [[Morquio syndrome]], [[mucopolysaccharidosis type IIIB]], [[Hurler syndrome]], [[Marfan's syndrome]], [[Mulibrey nanism]], [[ | |bgcolor="Beige"| [[1p36 deletion syndrome]], [[Alstrom syndrome]], [[Barth syndrome]], [[Becker muscular dystrophy]], [[Beckwith–Wiedemann syndrome]], [[cardiofaciocutaneous syndrome]], [[carnitine palmitoyl transferase deficiency]], [[congenital generalized lipodystrophy]], [[Costello syndrome]], [[Danon disease]], [[Desmin-related myofibrillar myopathy]], [[Duchenne muscular dystrophy]], [[Emery-Dreifuss muscular dystrophy, X-linked]], [[Fabry disease]], [[hypertrophic cardiomyopathy|familial hypertrophic cardiomyopathy]], [[friedreich ataxia]], [[fucosidosis]], [[Gaucher disease]], [[glycogenosis type 2]], [[glycogenosis type 2b]], [[hemochromatosis]], [[hereditary spherocytosis]], [[Hunter syndrome]], [[hypertrichotic osteochondrodysplasia]], [[infantile sialic acid storage disorder]], [[Isobutyryl-CoA dehydrogenase deficiency]], [[Laing distal myopathy]], [[long-chain acyl-CoA dehydrogenase deficiency]], [[Malonyl-CoA decarboxylase deficiency]], [[McLeod neuroacanthocytosis syndrome]], [[MELAS]], [[Morquio syndrome]], [[mucopolysaccharidosis type IIIB]], [[Hurler syndrome]], [[Marfan's syndrome]], [[Mulibrey nanism]], [[multiple lentigines syndrome]], [[myotonic dystrophy]], [[Naxos disease]], [[Noonan syndrome]], [[Pompe's disease]], [[Refsum disease]], [[Salih myopathy]], [[Sandhoff disease]], [[sickle cell disease]], [[Singleton-Merten syndrome]], [[Tay-Sachs' disease]], [[thalassemia]], [[very long-chain acyl-CoA dehydrogenase deficiency]], [[dilated cardiomyopathy|X-linked dilated cardiomyopathy]], [[Yunis-Varon syndrome]] | ||
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| '''Hematologic''' | | '''Hematologic''' | ||
|bgcolor="Beige"| [[Anemia]], [[ | |bgcolor="Beige"| [[Anemia]], [[hemochromatosis]], [[hereditary spherocytosis]], [[McLeod neuroacanthocytosis syndrome]], [[sickle cell disease]], [[thalassemia]] | ||
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Revision as of 02:30, 9 August 2013
Cardiomegaly Microchapters |
Diagnosis |
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Treatment |
Case Studies |
Cardiomegaly causes On the Web |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
There are numerous causes of cardiomegaly some of which include medications, genetic conditions, endocrine conditions, infectious processes, toxins and iatrogenic causes.
Causes
Life Threatening Causes
Common Causes
- Heart valve disease
- Cardiomyopathy
- Arrhythmia
- Pulmonary hypertension
- Anemia
- Thyrotoxicosis
- Hemochromatosis
- Amyloidosis
Causes by Organ System
Causes in Alphabetical Order
References
- ↑ Goel, Ramil; Alharthi, MohsenS; Jiamsripong, Panupong; Cha, Stephen; Mookadam, Farouk (2010). "Epicardial fat and its association with cardiovascular risk: A cross-sectional observational study". Heart Views. 11 (3): 103. doi:10.4103/1995-705X.76801. ISSN 1995-705X.