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5,483 Possible Causes for Cardiomyopathy, No Polydactyly, Onset of Renal Dysfunction in Early Childhood

  • Alstrom Syndrome

    Parental screening echocardiograms revealed no evidence of clinically silent dilated cardiomyopathy.[ncbi.nlm.nih.gov] Sufferers often develop early-onset type 2 diabetes, renal and hepatic dysfunction affecting the liver and kidneys, bladder and bowel problems, and cardiomyopathy, where the[dailymail.co.uk] […] childhood, progressive neurosensory hearing loss, diabetes mellitus, acanthosis nigricans, hypogonadism with normal secondary sex characteristics, and kyphoscoliosis without polydactyly[ncbi.nlm.nih.gov]

  • Microcephalic Primordial Dwarfism due to ZNF335 Deficiency

    , Dilated, 1ee MYH6 Cardiomyopathy, Dilated, 1g TTN Cardiomyopathy, Dilated, 1y TPM1 Cardiomyopathy, Familial Hypertrophic, 1 MYH6 Cardiomyopathy, Familial Hypertrophic, 14[selfdecode.com] […] syndrome Short rib-polydactyly syndrome, Beemer-Langer type Short rib-polydactyly syndrome, Majewski type Short rib-polydactyly syndrome, Saldino-Noonan type Short rib-polydactyly[se-atlas.de] 17; COXPD17 Combined oxidative phosphorylation deficiency-17 is an autosomal recessive disorder of mitochondrial dysfunction characterized by onset of severe hypertrophic cardiomyopathy[mendelian.co]

    Missing: Onset of Renal Dysfunction in Early Childhood
  • Spondyloepimetaphyseal Dysplasia-Hypotrichosis Syndrome

    1A Dilated cardiomyopathy 1A Dilated cardiomyopathy 1AA Dilated cardiomyopathy 1BB Dilated cardiomyopathy 1C Dilated cardiomyopathy 1D Dilated cardiomyopathy 1E Dilated cardiomyopathy[pentacorelab.hu] […] type A, Preaxial polydactyly type 3, Preaxial polydactyly type 4 GMPPB Limb-girdle muscular dystrophy-dystroglycanopathy, Muscular dystrophy-dystroglycanopathy (congenital[genda.com.ar] -14 Form of dilated cardiomyopathy MYH7 gene Form of scapuloperoneal myopathy Hypertrophic cardiomyopathy-1 Cardiomyopathy, dilated, 1S MYH9 gene Fechtner syndrome May-Hegglin[julesberman.blogspot.com]

    Missing: Onset of Renal Dysfunction in Early Childhood
  • Arthrogryposis due to Muscular Dystrophy

    […] muscular dystrophy, Reducing bod myopathy XL 26 62 FKBP10 Bruck syndrome 1, Osteogenesis imperfecta, type XI AR 20 44 FKTN Muscular dystrophy-dystroglycanopathy, Dilated cardiomyopathy[blueprintgenetics.com] Arthrogryposis can affect individual body parts, some joints even asymmetrically, and it is often seen combined with some other diseases like Marfan syndrome, syndactyly, polydactyly[physiobook.com] […] limbs, elbows extended, wrists flexed and ulnarly deviated, intrinsic plus deformity of hands, adducted thumbs, no flexion creases) Type III Full expression (type II) with polydactyly[orthobullets.com]

    Missing: Onset of Renal Dysfunction in Early Childhood
  • 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] Mirror hand is a congenital anomaly characterised by duplication of the ulnar ray, resulting in polydactyly and functional disability of the hand.[ncbi.nlm.nih.gov] Oudit, Hydroxychloroquine-Induced Cardiomyopathy: Case Report, Pathophysiology, Diagnosis, and Treatment, Canadian Journal of Cardiology, 30, 12, (1706), (2014).[doi.org]

    Missing: Onset of Renal Dysfunction in Early Childhood
  • Laurence Moon Syndrome

    Elbedour et al. reported 11 out of 22 patients (50%) had hypertrophy of the interventricular septum and dilated cardiomyopathy [ 6 ].[omicsonline.org] Figure 2: showing polydactyly in lower limbs Figure 3: showing polydactyly in left hand Figure 4: showing high arched palate.[medresearch.in] Anesthetic management of a patient with Bardet-Biedl syndrome and dilated cardiomyopathy.[joacp.org]

    Missing: Onset of Renal Dysfunction in Early Childhood
  • Limb-Girdle Muscular Dystrophy Type 2E

    LGMD1B patients often exhibit findings of both cardiomyopathy and dysrhythmia [ 7 ].[pubs.sciepub.com] […] calcification-moth-eaten skeletal dysplasia Microtubules Kinesin Charcot–Marie–Tooth disease 2A Hereditary spastic paraplegia 10 Dynein Primary ciliary dyskinesia Short rib-polydactyly[en.wikipedia.org] Calf hypertrophy, cardiomyopathy, respiratory impairment, tendon contractures, scoliosis, and exercise-induced myoglobinuria may be observed.[rarediseases.info.nih.gov]

    Missing: Onset of Renal Dysfunction in Early Childhood
  • Emery-Dreifuss Muscular Dystrophy Type 2

    An Indian family with an Emery-Dreifuss myopathy and familial dilated cardiomyopathy due to a novel LMNA mutation.[annalsofian.org] […] calcification-moth-eaten skeletal dysplasia Microtubules Kinesin Charcot–Marie–Tooth disease 2A Hereditary spastic paraplegia 10 Dynein Primary ciliary dyskinesia Short rib-polydactyly[en.wikipedia.org] Polydactyly 2 Short-Rib Thoracic Dysplasia 3 with or without Polydactyly 3 Short-Rib Thoracic Dysplasia 4 with or without Polydactyly 2 Short-Rib Thoracic Dysplasia 5 with[preventiongenetics.com]

    Missing: Onset of Renal Dysfunction in Early Childhood
  • Limb-Girdle Muscular Dystrophy Type 2F

    Keywords Delta-sarcoglycan Severe LGMD phenotype Cardiomyopathy References 1. Nigro V, Moreira ES, Piluso G, et al.[link.springer.com] […] calcification-moth-eaten skeletal dysplasia Microtubules Kinesin Charcot–Marie–Tooth disease 2A Hereditary spastic paraplegia 10 Dynein Primary ciliary dyskinesia Short rib-polydactyly[en.wikipedia.org] LGMD1B patients often exhibit findings of both cardiomyopathy and dysrhythmia [ 7 ] .[pubs.sciepub.com]

    Missing: Onset of Renal Dysfunction in Early Childhood
  • 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] […] calcification-moth-eaten skeletal dysplasia Microtubules Kinesin Charcot–Marie–Tooth disease 2A Hereditary spastic paraplegia 10 Dynein Primary ciliary dyskinesia Short rib-polydactyly[en.wikipedia.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]

    Missing: Onset of Renal Dysfunction in Early Childhood

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