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316 Possible Causes for Erythropoietic Porphyria, Myalgia, Peripheral Neuropathy

  • 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] Features of Textbook of Peripheral Neuropathy Include : ̈ Practical yet comprehensiveóan accessible ìgo-toî reference for clinicians ̈ Covers all clinically relevant peripheral[books.google.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]

  • Porphyria

    Desnick, Congenital erythropoietic porphyria: Recent advances, Molecular Genetics and Metabolism, 10.1016/j.ymgme.2018.12.008, (2018).[doi.org] Any part of the nervous system may be involved with autonomic and peripheral neuropathy. Peripheral neuropathy may be symmetric or asymmetric.[symptoma.com] Part 1: peripheral neuropathies, Neurological Sciences, 10.1007/s10072-019-03778-7, (2019). Maureen B.[doi.org]

  • Acute Intermittent Porphyria

    There are seven main types of porphyrias; acute intermittent porphyria and plumboporphyria are predominantly neuropsychiatric; congenital erythropoietic porphyria, porphyria[ncbi.nlm.nih.gov] Both had a very poor quality of life as a result of years of frequent acute porphyria symptoms, chronic peripheral neuropathy and renal failure requiring dialysis.[ncbi.nlm.nih.gov] 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]

  • Erythropoietic Coproporphyria

    Prenatal exclusion of congenital erythropoietic porphyria (Günther's disease) in a fetus at risk. Hum. Genet. 53 (1980) 217–221 Google Scholar Doss, M.[link.springer.com] Features of Textbook of Peripheral Neuropathy Include : ̈ Practical yet comprehensiveóan accessible ìgo-toî reference for clinicians ̈ Covers all clinically relevant peripheral[books.google.de] Molecular genetics of congenital erythropoietic porphyria.[ncbi.nlm.nih.gov]

  • Lead Poisoning

    In the described case of the death of a 41-year-old-man, no enzymatic disturbances characteristic of congenital erythropoietic porphyria were ascertained, and furthermore,[ncbi.nlm.nih.gov] Simultaneously, the child showed anemia, encephalopathy, and peripheral neuropathy with albuminocytological dissociation mimicking Guillain-Barré syndrome.This case suggests[ncbi.nlm.nih.gov] Linear regression analysis showed log of BLL was significantly associated with abdominal pain, myalgia and anorexia.[ncbi.nlm.nih.gov]

  • Primary Hyperoxaluria

    Lipase Deficiency Congenital Erythropoietic Porphyria; UROS mutation: c.331G A Glycogen Storage Disease Type IV Mucopolysaccharidosis Type I (MPS I) Mucopolysaccharidosis[optimal-selection.com] Retinal epithelium and the macula  diminished visual acuity Hypothyroidism, peripheral neuropathy, dental problems Skin manifestations Livedo reticularis, peripheral[slideshare.net] […] joints, the retina, and the central nervous system, causing complications in the form of cardiomyopathy, disturbances in the cardiac conduction system, retinopathy, severe myalgia[symptoma.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] Electrophysiologic studies demonstrated a peripheral neuropathy with features of axonal degeneration and demyelination.[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]

  • Myoadenylate Deaminase Deficiency

    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] Neuropathy 405 Case 64 A Man with a Neuropathy Weight Loss and Lung Nodules 411 Case 65 A Woman with Difficulty Walking and Ataxia 415 Case 66 A Man with Progressive Neuropathy[books.google.com] 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]

  • Muckle-Wells Syndrome

    Myalgia, arthralgias and distal edema are very common. With age, patients develop eythematous band over the hands as well as digital clubbing.[orpha.net] porphyria pophyria charac by SEVERE PHOTOSENSITIVITY sun exposure -- vesicles bullae develop erythrodontia red-stained teeth porphyria charac by photosensitivity vesicle[quizlet.com] Pendred Syndrome Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss Perrault Syndrome Renal tubular acidosis with deafness Seizures, Sensorineural Deafness, Ataxia[genedx.com]

  • Glycogen Storage Disease due to Phosphoglycerate Mutase Deficiency

    Porphyria Congenital Erythropoietic Porphyria, Mild, Cutaneous-only Congenital Fast Channel Myasthenic Syndrome Congenital Heart Defects Congenital Heart Disease Heterotaxy[sequencing.com] Peripheral Neuropathy Natural Treatment Options This guide will help millions of people understand this condition so that they can take control of their lives and make informed[rrnursingschool.biz] We present a family with muscle phosphoglycerate mutase (PGaM) deficiency, mild glycogen storage and some exertional myalgia.[ncbi.nlm.nih.gov]

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