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108 Possible Causes for Pseudohypertrophy of Calf Muscles

  • Becker Muscular Dystrophy

    , fatigue and pseudohypertrophy of calf muscles[medical-dictionary.thefreedictionary.com] ) in calf muscles Muscle wasting that begins in the legs and pelvis, then progresses to the muscles of the shoulders, neck, arms, and respiratory system Laboratory tests that[rarediseases.info.nih.gov] Becker's muscular dystrophy Neurology An X-linked condition characterized by slowly progressive muscle weakness of the legs and pelvis, difficulty walking, mental retardation[medical-dictionary.thefreedictionary.com]

  • Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2E

    […] recessive inheritance 0000007 Calf muscle pseudohypertrophy 0003707 Juvenile onset Signs and symptoms begin before 15 years of age 0003621 Limb-girdle muscle weakness 0003325[rarediseases.info.nih.gov] License: Public Domain On examination, you may find pseudohypertrophy of gastrocnemius (calf) muscles. Examine the mental state of the child as retardation is common.[lecturio.com] 0001638 Dilated cardiomyopathy Stretched and thinned heart muscle 0001644 Myoglobinuria 0002913 Percent of people who have these symptoms is not available through HPO Autosomal[rarediseases.info.nih.gov]

  • Duchenne Muscular Dystrophy

    Early signs may include pseudohypertrophy (enlargement of calf muscles), low endurance, and difficulties in standing unaided or inability to ascend staircases.[disabled-world.com] There is pseudohypertrophy of tongue (macroglossia in 30% cases) and calf muscles (60% cases).[symptoma.com] Clinical examination reveals muscle pseudohypertrophy affecting the calf muscles and there may be atrophy of more proximal muscles such as the quadriceps.[orpha.net]

  • Muscular Dystrophy

    Pseudohypertrophy of the calf muscles is due to fibrous tissue and fat infiltration. Involvement of the heart consists of usually terminal cardiomyopathy.[icd9data.com] Calf muscles initially enlarge and the enlarged muscle tissue is eventually replaced with fat and connective tissue (pseudohypertrophy).[genome.gov]

  • Hyaline Body Myopathy

    muscle pseudohypertrophy 0003707 Centrally nucleated skeletal muscle fibers 0003687 Congestive heart failure Cardiac failure Cardiac failures Heart failure [ more ] 0001635[rarediseases.info.nih.gov] […] available through HPO Abnormality of the cardiovascular system Cardiovascular abnormality 0001626 Autosomal dominant inheritance 0000006 Autosomal recessive inheritance 0000007 Calf[rarediseases.info.nih.gov]

  • Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2C

    License: Public Domain On examination, you may find pseudohypertrophy of gastrocnemius (calf) muscles. Examine the mental state of the child as retardation is common.[lecturio.com]

  • Limb-Girdle Muscular Dystrophy due to POMK Deficiency

    muscle pseudohypertrophy Attention deficit hyperactivity disorder Chorea Poor speech Hepatic steatosis Unsteady gait Carious teeth Abnormality of movement Abnormality of[mendelian.co] […] onset Recurrent ear infections Asymmetric growth Vomiting X-linked recessive inheritance Hyperactivity EEG abnormality Achalasia Nyctalopia Chest pain Speech apraxia Tremor Calf[mendelian.co]

  • Spinal Muscular Atrophy Type 3

    Spinal musular atrophies are a group of genetic disorders distinguished by progressive degeneration of anterior horn cells in the spinal cord. Proximal weakness of the extremities that may require use of assistive devices and minimal respiratory difficulties appearing between 18 months and 30 years of age are[…][symptoma.com]

  • Spinal Muscular Atrophy

    The full text of this article hosted at iucr.org is unavailable due to technical difficulties. Histone Deacetylase Inhibition Activity and Molecular Docking of ( E )‐Resveratrol: Its Therapeutic Potential in Spinal Muscular Atrophy First published: 05 February 2009 Cited by: 25 Abstract Spinal muscular atrophy is an[…][doi.org]

  • Adult Spinal Muscular Atrophy

    Adult spinal muscular atrophy is a genetic neurodegenerative disorder characterized by muscle wasting and weakness. In adults, normal life expectancy is achieved, as only mild weakness may be encountered. The diagnosis rests on confirming genetic mutations. Adult spinal muscular atrophy or spinal muscular atrophy[…][symptoma.com]

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