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360 Possible Causes for Erythropoietic Porphyria, Myalgia

  • 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] Four patients were assessed as having AEs possibly related to study drug, including injection site reaction (mild and self-limiting), hypersensitivity, myalgia, headache,[dddmag.com]

  • Porphyria

    Desnick, Congenital erythropoietic porphyria: Recent advances, Molecular Genetics and Metabolism, 10.1016/j.ymgme.2018.12.008, (2018).[doi.org] What is congenital erythropoietic porphyria?[britishskinfoundation.org.uk] Erythropoietic porphyrias include erythropoietic protoporphyria and congenital erythropoietic porphyria.[ghr.nlm.nih.gov]

  • 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] 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] 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]

  • 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] Molecular genetics of congenital erythropoietic porphyria.[ncbi.nlm.nih.gov] From her mother she inherited the trait of hereditary coproporphyria; from both parents she inherited the trait of congenital erythropoietic porphyria (Günther disease).[link.springer.com]

  • 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] 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] CONCLUSION: MAD deficiency must be ruled out in every patient with exertional myalgia and increased CK which normalizes when asymptomatic.[pesquisa.bvsalud.org]

  • Muckle-Wells Syndrome

    porphyria pophyria charac by SEVERE PHOTOSENSITIVITY sun exposure -- vesicles bullae develop erythrodontia red-stained teeth porphyria charac by photosensitivity vesicle[quizlet.com] 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 porphyria cutanea tarda rare serious dz caused by accumulation of proteins as abnormal insoluble fibers (amyloids) - local or systemic a/w multiple myeloma -- get[quizlet.com]

  • Lead Poisoning

    Linear regression analysis showed log of BLL was significantly associated with abdominal pain, myalgia and anorexia.[ncbi.nlm.nih.gov] 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] […] motility Abnormal sperm Heme Synthesis Anemia Erythrocyte protoporphyrin elevation Renal Effects Chronic nephropathy with proximal tubular damage Hypertension Other Arthralgia Myalgia[health.ny.gov]

  • Hereditary Coproporphyria

    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] 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] 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]

  • Glycogen Storage Disease due to Phosphoglycerate Mutase Deficiency

    We present a family with muscle phosphoglycerate mutase (PGaM) deficiency, mild glycogen storage and some exertional myalgia.[ncbi.nlm.nih.gov] Uroporphyrinogen decarboxylase : Porphyria cutanea tarda; MIN:176090. Uroporphyrinogen-III synthase : Congenital erythropoietic porphyria (CEP); MIN:263700.[changbioscience.com] A 52-year-old African-American woman presented with exertional muscle contractures, myalgias, and weakness since childhood including an episode of rhabdomyolysis.[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] […] 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] ; HMBS mutation: c.844delGAG Acute Intermittent Porphyria; HMBS mutation c.107_110delACAG Acute Intermittent Porphyria; HMBS mutation c.826-1G A Chylomicronemia, Lipoprotein[optimal-selection.com]

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