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4,673 Possible Causes for Cardiomyopathy, Green Jaundice, Increased Serum Creatine Phosphate

  • Autosomal Dominant Limb-Girdle Muscular Dystrophy Type 1B

    acid synthesis defect with cholestasis and malabsorption Biotin-thiamine-responsive basal ganglia disease Biotinidase deficiency Björnstad syndrome Blue diaper syndrome Brachytelephalangic[se-atlas.de] Emery-Dreifuss muscular dystrophy (EDMD) and limb-girdle muscular dystrophy type 1B (LGMD1B) are characterized by cardiac dysrhythmias, late-onset cardiomyopathy, slowly progressive[ncbi.nlm.nih.gov] LGMD1B is caused by variants in the LMNA gene, and there is considerable phenotypic overlap with the laminopathies, dilated cardiomyopathy and the autosomal dominant form[exeterlaboratory.com]

  • Autosomal Dominant Limb-Girdle Muscular Dystrophy Type 1H

    jaundice Green monkey disease Greig cephalopolysyndactyly syndrome Greither disease GRFoma GRF tumor Grisart-Destrée syndrome Griscelli-Pruniéras syndrome Griscelli-Pruniéras[orpha.net] LGMD1B patients often exhibit findings of both cardiomyopathy and dysrhythmia [ 7 ].[pubs.sciepub.com] cardiomyopathy 7, 2 Nemaline myopathy 4, 5 Tropomyosin Hypertrophic cardiomyopathy 3 Nemaline myopathy 1 Titin Hypertrophic cardiomyopathy 9 Other Fibrillin Marfan syndrome[en.wikipedia.org]

  • Duchenne Muscular Dystrophy

    BACKGROUND: Duchenne muscular dystrophy (DMD) is frequently complicated by development of a cardiomyopathy.[ncbi.nlm.nih.gov] She was treated for peripartum cardiomyopathy (PPCM) with angiotensin converting enzyme inhibitors (ACEi), beta-blockers and diuretics with normalisation of her cardiac function[ncbi.nlm.nih.gov] We present the case of a 29-year-old man with mutation-positive Duchenne muscular dystrophy and mutation-positive hypertrophic cardiomyopathy.[ncbi.nlm.nih.gov]

    Missing: Green Jaundice
  • Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2E

    Calf hypertrophy, cardiomyopathy, respiratory impairment, tendon contractures, scoliosis, and exercise-induced myoglobinuria may be observed.[rarediseases.info.nih.gov] LGMD1B patients often exhibit findings of both cardiomyopathy and dysrhythmia [ 7 ].[pubs.sciepub.com] Disease of the heart muscle 0001638 Dilated cardiomyopathy Stretched and thinned heart muscle 0001644 Myoglobinuria 0002913 Percent of people who have these symptoms is not[rarediseases.info.nih.gov]

    Missing: Green Jaundice
  • Emery-Dreifuss Muscular Dystrophy Type 1

    Abstract The original Virginia family with X‐linked muscular dystrophy with early contractures and cardiomyopathy (Emery‐Dreifuss type) has been reinvestigated 25 years later[doi.org] […] elbow, and neck tendons, beginning during early childhood and leading to limited joint movement; and cardiac anomalies (conduction defects, rhythm disturbances, and dilated cardiomyopathy[link.springer.com] The findings confirm that a cardiomyopathy, presenting most often as atrioventricular block, is a significant feature of the disease, which is characterized by the triad of[doi.org]

    Missing: Green Jaundice
  • Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2C

    Symptoms may additionally include: enlargement (hypertrophy) of the calf muscle and tongue, diseases of the heart muscle ( cardiomyopathy ), and respiratory abnormalities.[rarediseases.info.nih.gov] Patients may also experience cardiomyopathy and lung disease, and may develop scoliosis and joint contractures as the disease progresses.[sema4genomics.com] LGMD1B patients often exhibit findings of both cardiomyopathy and dysrhythmia [ 7 ].[pubs.sciepub.com]

    Missing: Green Jaundice
  • Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2I

    Clinical features include weakness of the hip and shoulder girdle, difficulty walking, spinal abnormalities including scoliosis, lordosis and kyphosis, and cardiomyopathy.[sema4genomics.com] LGMD1B patients often exhibit findings of both cardiomyopathy and dysrhythmia [ 7 ].[pubs.sciepub.com] Cardiomyopathy, familial hypertrophic (CAV3) Dilated cardiomyopathy, 1I (DES) Cardiomyopathy, dilated, 3B, X-linked (DMD) Cardiomyopathy, familial hypertrophic, 1 (MYH7)[meduniwien.ac.at]

    Missing: Green Jaundice
  • Glycogen Storage Disease Type 2

    , lysosomal disease with hypertrophic cardiomyopathy, glycogen storage disease with hypertrophic cardiomyopathy, lysosomal glycogen storage disease Prende il nome da Johannes[commons.wikimedia.org] If left untreated, affected infants often die from hypertrophic cardiomyopathy during their first year of life.[symptoma.com] The infantile form is fatal in infancy and presents with hypotonia and a hypertrophic cardiomyopathy (cardiomyopathy, hypertrophic).[icd10data.com]

    Missing: Green Jaundice
  • Becker Muscular Dystrophy

    Patients with Becker muscular dystrophy-related cardiomyopathy typically survive into their 30s, when they succumb to complications of cardiomyopathy or receive heart transplants[ncbi.nlm.nih.gov] Ivabradine normalizes sinus tachycardia and resolves heart failure in patients with dilated cardiomyopathy from BMD.[ncbi.nlm.nih.gov] A 54-year-old patient with Becker muscular dystrophy and dilated cardiomyopathy underwent laparoscopic cholecystectomy under total intravenous anesthesia.[ncbi.nlm.nih.gov]

    Missing: Green Jaundice
  • Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2N

    acid synthesis defect with cholestasis and malabsorption Biotin-thiamine-responsive basal ganglia disease Biotinidase deficiency Björnstad syndrome Blue diaper syndrome Brachytelephalangic[se-atlas.de] LGMD1B patients often exhibit findings of both cardiomyopathy and dysrhythmia [ 7 ].[pubs.sciepub.com] Cardiomyopathy, familial hypertrophic (CAV3) Dilated cardiomyopathy, 1I (DES) Cardiomyopathy, dilated, 3B, X-linked (DMD) Cardiomyopathy, familial hypertrophic, 1 (MYH7)[meduniwien.ac.at]

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