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47 Possible Causes for Erythropoietic Porphyria, Myalgia, Respiratory Muscle Paralysis

  • Acute Hepatic Porphyria

    porphyria E80.1 Porphyria cutanea tarda E80.2 Other and unspecified porphyria E80.20 Unspecified porphyria E80.21 Acute intermittent (hepatic) porphyria E80.3 Defects of[icd10data.com] Possibly or definitely related AEs reported in two or more cases were injection site reactions and myalgia; all of these events were mild.[businesswire.com] Proximal myopathy affecting the arms can progress to quadraparesis, respiratory muscle paralysis and respiratory arrest.[patient.info]

  • Porphyria

    Desnick, Congenital erythropoietic porphyria: Recent advances, Molecular Genetics and Metabolism, 10.1016/j.ymgme.2018.12.008, (2018).[doi.org] Proximal myopathy affecting the arms can progress to quadraparesis, respiratory muscle paralysis and respiratory arrest.[patient.info] What is congenital erythropoietic porphyria?[britishskinfoundation.org.uk]

  • Acute Intermittent Porphyria

    Her abdominal pain and myalgia subsided on the third day of dialysis. Her lower limb muscle power improved and she became ambulant by the fourth day.[ncbi.nlm.nih.gov] Over the next 15 days, she developed respiratory muscle paralysis, was intubated and put on mechanical ventilation.[joacp.org] There are seven main types of porphyrias; acute intermittent porphyria and plumboporphyria are predominantly neuropsychiatric; congenital erythropoietic porphyria, porphyria[ncbi.nlm.nih.gov]

  • Myoadenylate Deaminase Deficiency

    A diagnosis of tension myalgia or myofascial-type pain is often considered when no objective findings are seen in the evaluation.[ncbi.nlm.nih.gov] paralysis.[sites.google.com] porphyria E80.1 Porphyria cutanea tarda E80.2 Other and unspecified porphyria E80.20 Unspecified porphyria E80.21 Acute intermittent (hepatic) porphyria E80.3 Defects of[icd10data.com]

  • Hereditary Coproporphyria

    From her mother she inherited the trait of hereditary coproporphyria; from both parents she inherited the trait of congenital erythropoietic porphyria (Günther disease).[ncbi.nlm.nih.gov] Neurological manifestations can affect the central nervous system as much as the peripheral nervous system (myalgia, paresis, ascending flaccid paralysis of the limbs, or[orpha.net] […] of the arms and legs, body trunk, and respiratory muscles.[rarediseases.info.nih.gov]

  • Hepatoerythropoietic Porphyria

    […] paralysis Urinary retention Abnormal urinary color Psychotic episodes Hypertensive crisis Elevated urinary delta-aminolevulinic acid Paralytic ileus Micrognathia Focal seizures Myalgia[mendelian.co] Erythropoietic porphyrias include erythropoietic protoporphyria and congenital erythropoietic porphyria.[ghr.nlm.nih.gov] Certain clinical and biochemical features distinguish HEP from erythropoietic porphyria and erythropoietic protoporphyria, the two diseases with which HEP is often confused[ncbi.nlm.nih.gov]

  • Erythema Chronicum Migrans

    Back to Top Endocrine and Metabolic Disease Porphyrias Porphyrias are inherited or acquired disorders of heme biosynthesis and can be erythropoietic, hepatic, or mixed in[clevelandclinicmeded.com] The syndrome may include advancing erythematous rash stemming from an apparent insect bite, hyperesthesias, myalgias, malaise, fever, lymphadenopathy, and, rarely, meningitis[ncbi.nlm.nih.gov] Tick neurotoxin Incubation period : 2–7 days Weakness in lower extremities ascending flaccid paralysis that progresses rapidly over 24–48 hours can lead to respiratory failure[amboss.com]

  • Photosensitivity Disorder

    Urticarial responses are typical for solar urticaria; but urticarial lesions can also occur in erythropoietic porphyria.[accessemergencymedicine.mhmedical.com] ., arthralgias, myalgias, arthritis) and constitutional (e.g., fever, malaise, anorexia, weight loss) symptoms. 17,18 Certain agents are more closely linked with specific[uspharmacist.com] , paralysis and hazardous respiratory problems.[oncosec.com]

  • Autosomal Dominant Myoglobinuria

    , Acute Hepatic 2 Porphyria, Congenital Erythropoietic 3 Portal hypertension, noncirrhotic 2 Posterior Column Ataxia With Retinitis Pigmentosa 6 Potassium Aggravated Myotonia[preventiongenetics.com] Suite gene sharing: Human phenotypes related to Myoglobinuria, Autosomal Dominant: 33 # Description HPO Frequency HPO Source Accession 1 muscle weakness 33 HP:0001324 2 myalgia[malacards.org] In ALS, the most frequent form of MND, degeneration involves both upper and lower motor neurons and results in progressive muscle weakness, paralysis, and death from respiratory[mayocliniclabs.com]

  • Distal Myopathy Type 3

    (ADP), Acute intermittent porphyria (AIP), Congenital erythopoietic porphyria (CEP), Erythropoietic protoporphyria (EPP), Hereditary coproporphyria (HCP) Porphyria cutanea[orphananesthesia.eu] Organ system Disease Symptoms History Physical Examination Diagnosis Age of onset Muscle weakness Fever Myalgia Contractures Gait abnormality Neuropathy Atrophy Stiffness[wikidoc.org] […] associated with respiratory distress due to diaphragmatic paralysis. [1] Myasthenia Gravis [4] This is a group of diseases with mutations in genes leading to neuromuscular[explainmedicine.com]

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