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706 Possible Causes for Cardiomyopathy, Joint Stiffness, Progressive Contractures

  • Rheumatoid Arthritis

    (0.50–0.66) Cardiac diseases Acute MI 2.6 (0.9) 7.8 (1.3) 0.31 (0.27–0.34) Chronic ischemic heart disease 4.0 (0.9) 11.7 (0.7) 0.32 (0.29–0.35) Congestive heart failure/cardiomyopathy[ncbi.nlm.nih.gov] Erosion of the articular cartilage, together with ligamentous changes, result in deformity and contractures. As the disease progresses, pain and deformity increase.[orthoinfo.aaos.org] The common signs include joint stiffness, swelling, pain, redness and warmth. These are typical hallmarks of inflammation.[techtimes.com]

  • Congenital Muscular Dystrophy

    cardiomyopathy died at the ages of 2 years 1 month, and 7 years 4 months respectively.[ncbi.nlm.nih.gov] We report the first known Egyptian patient with FCMD, established by clinical features of generalized weakness, pseudohypertrophy of calf muscles, progressive joint contractures[ncbi.nlm.nih.gov] CMD results in overall muscle weakness with possible joint stiffness or looseness.[mda.org]

  • Mucopolysaccharidosis 2

    Diarrhea Short stature Skeletal deformities Joint stiffness Inguinal or umbilical hernia Developmental delay Intellectual disability Hyperactivity Seizures Hepatomegaly Cardiomyopathy[symptoma.com] Flexion contractures. Progressive deafness - usually mixed sensorineural/conductive variety.[patient.info] Mucopolysaccharidosis II affects multiple organs and physiologic systems and has a variable age of onset and variable rate of progression.[pediatrics.aappublications.org]

  • Mucopolysaccharidosis

    Cardiac involvement is common in MPS patients and usually consists of progressive valvular thickening with incompetence and cardiomyopathy.[ncbi.nlm.nih.gov] ; hip containment surgeries; corrective osteotomy for progressive valgus deformity at the knee; posterior spinal fusion Multispecialty care is mandatory for these patients[emedicine.medscape.com] […] mucopolysaccharidosis type VI) is a rare lysosomal storage disorder in which the pathologic storage of glycosaminoglycans in various tissues can lead to severe symptoms, including cardiomyopathy[ncbi.nlm.nih.gov]

  • Systemic Scleroderma

    , rare rheumatologic disease, lung disease, autoimmune cardiomyopathy Authority control Q5340515 Reasonator Scholia Statistics Subcategories This category has the following[commons.wikimedia.org] With disease progression, ulcerations over joints and flexion contractures of the fingers, wrists, and elbows may occur.[aafp.org] Other signs and symptoms of systemic scleroderma from internal organ involvement may include: Joint inflammation with stiffness and pain Sores (ulcers), mostly on the fingertips[my.clevelandclinic.org]

  • Mucopolysaccharidosis 1

    Cardiomyopathy and coronary heart disease. Hepatosplenomegaly.[patient.info] Currently, no patient has any clinical evidence of cardiomyopathy.[adc.bmj.com] stiffness The cause of MPS I is inherited genetic mutations on chromosome 4 that leads to deficiency in the lysosomal enzyme a-L-iduronidase.[medicinenet.com]

  • Mucopolysaccharidosis 1H

    Corneal opacities, hepatosplenomegaly, cardiomyopathy and upper airway obstruction are present.[pedsradiology.com] The two patients with graft failure (patients 14 and 15) experienced progressive contractures in almost all joints.[ojrd.biomedcentral.com] Joint stiffness: Joint stiffness occurs by the age of 2 years and is progressive. There is a characteristic claw-hand deformity due to phalangial dysostosis.[symptoma.com]

  • Mucopolysaccharidosis 6

    Additional heart abnormalities can include disease or weakening of the heart muscle (cardiomyopathy) and endocardial fibroelastosis.[rarediseases.org] , hirsutism, joint contractures, hepatosplenomegaly, short stature, and skeletal, respiratory, and cardiac abnormalities, with a characteristic pattern of a chronic and progressive[scielo.br] The major clinical manifestations are corneal clouding, joint stiffness, and a skeletal dysplasia known as dysostosis multiplex.[egl-eurofins.com]

  • Emery-Dreifuss Muscular Dystrophy

    Emery-Dreifuss muscular dystrophy: humeroperoneal muscular atrophy and weakness, neck and elbow contractures with sinus bradycardia, first-degree atrioventricular block, and dilated cardiomyopathy[ncbi.nlm.nih.gov] Abstract Emery-Dreifuss muscular dystrophy (EDMD) is a neuromuscular disorder resulting in progressive muscle weakness, contractures, and cardiomyopathy.[ncbi.nlm.nih.gov] The condition causes slowly progressive (worsening) weakness in the muscles of the shoulders, upper arms, and lower legs and joint stiffness (contractures).[nationwidechildrens.org]

  • Arthrogryposis Multiplex Congenita

    AMC is rarely associated with cardiomyopathy.[ncbi.nlm.nih.gov] Abstract Arthrogryposis multiplex congenita (AMC) is a rare disorder characterized by non-progressive, multiple contractures.[ncbi.nlm.nih.gov] Arthrogryposis multiplex congenita (AMC) is a complex disorder that leads to joint stiffness and deformities in 2 or more joints in afflicted children.[ncbi.nlm.nih.gov]

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