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47 Possible Causes for Amyotrophic Lateral Sclerosis with Polyglucosan Bodies, Asymptomatic Hyperammonemia (2- to 5-fold Increase)

Did you mean: Amyotrophic Lateral Sclerosis with Polyglucosan Bodies, Asymptomatic Hyperammonemia (2- to 5-fold Increase

  • Unverricht-Lundborg Syndrome

    Alexander Disease Amyotrophic Lateral Sclerosis with Polyglucosan Bodies Canavan disease Cerebrocortical Degeneration of Infancy Cockayne syndrome Congenital Muscular Dystrophy[rgd.mcw.edu]

    Missing: Asymptomatic Hyperammonemia (2- to 5-fold Increase)
  • Adult Polyglucosan Body Disease

    lateral sclerosis and who was subsequently found to have adult polyglucosan body disease (APGBD) upon postmortem neuropathologic explorations.[ncbi.nlm.nih.gov] Except in type IV glycogenosis, the causes for accumulation of polyglucosan bodies are unknown.[ncbi.nlm.nih.gov] McDonald TD, Faust PL, Bruno C, DiMauro S, Goldman JE (1993) Polyglucosan body disease simulating amyotrophic lateral sclerosis.[link.springer.com]

    Missing: Asymptomatic Hyperammonemia (2- to 5-fold Increase)
  • Amyotrophic Lateral Sclerosis Type 1

    Amyotrophic Lateral Sclerosis Synonyms of Amyotrophic Lateral Sclerosis ALS Amyotrophic Lateral Sclerosis-Polyglucosan Bodies Aran-Duchenne Muscular Atrophy Gehrig's Disease[rarediseases.org] Lou Gehrig's Disease Motor System Disease (Focal and Slow) Subdivisions of Amyotrophic Lateral Sclerosis Benign Focal Amyotrophy of ALS Infantile Spinal Muscular Atrophy,[rarediseases.org]

    Missing: Asymptomatic Hyperammonemia (2- to 5-fold Increase)
  • Autosomal Recessive Lower Motor Neuron Disease with Childhood Onset

    Polyglucosan body disease simulating amyotrophic lateral sclerosis.[ncbi.nlm.nih.gov] Amyotroph Lateral Scler Other Motor Neuron Disord. 2004; 5 :208–12. [ PubMed : 15799548 ] Tonin P, Tomelleri G, Vio M, Rizzuto N. Polyglucosan body myopathy: a new case.[ncbi.nlm.nih.gov] Survival of 793 patients with amyotrophic lateral sclerosis diagnosed over a 28-year period.[ncbi.nlm.nih.gov]

    Missing: Asymptomatic Hyperammonemia (2- to 5-fold Increase)
  • Amyotrophic Lateral Sclerosis

    Polyglucosan body disease simulating amyotrophic lateral sclerosis.[ncbi.nlm.nih.gov] Amyotroph Lateral Scler Other Motor Neuron Disord. 2004; 5 :208–12. [ PubMed : 15799548 ] Tonin P, Tomelleri G, Vio M, Rizzuto N. Polyglucosan body myopathy: a new case.[ncbi.nlm.nih.gov] Survival of 793 patients with amyotrophic lateral sclerosis diagnosed over a 28-year period.[ncbi.nlm.nih.gov]

    Missing: Asymptomatic Hyperammonemia (2- to 5-fold Increase)
  • Motor Neuron Disease

    Eight patients with concurrent amyotrophic lateral sclerosis (ALS) and chorea had been described prior to 1993, when genetic testing for HD first became available. 2 Rubio[jamanetwork.com] body disease, dentatorubralpallidoluysian atrophy, and other spinocerebellar ataxias.[jamanetwork.com] […] can be seen in a variety of neurological disorders, such as Wilson disease, systemic lupus erythematosus, endocrinopathies, neuroacanthocytosis, GM2 gangliosidosis, adult polyglucosan[jamanetwork.com]

    Missing: Asymptomatic Hyperammonemia (2- to 5-fold Increase)
  • Primary Lateral Sclerosis

    E deficiency Lathyrism Neurodegenerative Amyotrophic lateral sclerosis Absence of: Marked fasciculations or muscle atrophy Sensory signs on exam Family history of similar[ncbi.nlm.nih.gov] body disease Infectious / Inflammatory Tropical Spastic Paraperesis (HTLV 1/2) HIV Syphilis Sarcoidosis Metabolic/Toxic Subacute combined degeneration (B12 deficiency) Vitamin[ncbi.nlm.nih.gov] Demyelinating Multiple Sclerosis/ Primary Progressive MS Vitamin E deficiency Hereditary Hereditary spastic paraplegia Leukodystrophy (metachromatic, adrenoleukodystrophy) Polyglucosan[ncbi.nlm.nih.gov]

    Missing: Asymptomatic Hyperammonemia (2- to 5-fold Increase)
  • Aprosencephaly and Cerebellar Dysgenesis

    […] to, 25; ALS25 OMIM:205250 Amyotrophic Lateral Sclerosis with Polyglucosan Bodies OMIM:162100 Amyotrophy, Hereditary Neuralgic; HNA OMIM:602440 Amyotrophy, Monomelic OMIM:[informatics.jax.org] Lateral Sclerosis-Parkinsonism/Dementia Complex 1 OMIM:617892 Amyotrophic Lateral Sclerosis, Susceptibility to, 24; ALS24 OMIM:617921 Amyotrophic Lateral Sclerosis, Susceptibility[informatics.jax.org] 608627 Amyotrophic Lateral Sclerosis 8; ALS8 OMIM:611895 Amyotrophic Lateral Sclerosis 9; ALS9 OMIM:205200 Amyotrophic Lateral Sclerosis, Juvenile, with Dementia OMIM:105500 Amyotrophic[informatics.jax.org]

    Missing: Asymptomatic Hyperammonemia (2- to 5-fold Increase)
  • Glycogen Storage Disease due to Muscle Beta-Enolase Deficiency

    A late-onset form of GSD IV causes adult polyglucosan body disease (APBD), a motor neuron disease that can mimic amyotrophic lateral sclerosis.[medlink.com] […] lower motor neurone dysfunction (sometimes simulating amyotrophic lateral sclerosis), sensory loss, sphincter problems and, inconsistently, dementia.  In APBD, polyglucosan[slideshare.net] . • GSD III and GSD IV (branching enzyme deficiency) cause congenital or later-onset weakness, sometimes accompanied by liver disease or cardiomyopathy.[medlink.com]

    Missing: Asymptomatic Hyperammonemia (2- to 5-fold Increase)
  • Glycogen Storage Disease due to Phosphoglycerate Kinase 1 Deficiency

    A late-onset form of GSD IV causes adult polyglucosan body disease (APBD), a motor neuron disease that can mimic amyotrophic lateral sclerosis.[medlink.com] […] lower motor neurone dysfunction (sometimes simulating amyotrophic lateral sclerosis), sensory loss, sphincter problems and, inconsistently, dementia.  In APBD, polyglucosan[slideshare.net] . • GSD III and GSD IV (branching enzyme deficiency) cause congenital or later-onset weakness, sometimes accompanied by liver disease or cardiomyopathy.[medlink.com]

    Missing: Asymptomatic Hyperammonemia (2- to 5-fold Increase)

Further symptoms