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52 Possible Causes for Erythropoietic Porphyria, Generalized Motor Seizure, 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]

  • 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] There are seven main types of porphyrias; acute intermittent porphyria and plumboporphyria are predominantly neuropsychiatric; congenital erythropoietic porphyria, porphyria[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]

  • 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] Linear regression analysis showed log of BLL was significantly associated with abdominal pain, myalgia and anorexia.[ncbi.nlm.nih.gov] When Uroporphyrinogen III synthase is deficient, as in congenital erythropoietic Porphyria (Gunther’s disease), hydroxymethylbilane rapidly undergoes nonenzymatic ring closure[usmle.biochemistryformedics.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] 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]

  • Polycythemia Neonatorum

    Protoporphyria (Porphyria) Esophageal Achalasia (Achalasia) Esophageal Atresia Esophageal Cancer Esophageal Perforation Esophageal Spasm Esophageal Stricture - Benign Esophagitis[ezesauna.com] Posted On February 18, 2015 Free Searchable Online Version Of The 2009 Icd-9-cm 729.1 Myalgia And Myositis, Unspecified. 04 Num Summary: 776.4 Polycythemia Neonatorum - Icd[ygsearch.com] Erythremia (Polycythemia Vera) Erythroblastosis Fetalis Erythrocytosis Megalosplenica (Polycythemia Vera) Erythroderma (Exfoliative Dermatitis) Erythroplasia of Queyrat Erythropoietic[ezesauna.com]

  • Pallister W Syndrome

    Porphyria Cutanea Tarda Porphyria, Acute Intermittent Porphyria, ALA-D Porphyria, Congenital Erythropoietic Porphyria, Hereditary Coproporphyria Porphyria, Variegate Post[medschool.umaryland.edu] An influenzalike syndrome, consisting of fever, chills, myalgia, nausea, vomiting, and diarrhea, may be noted in 20% of patients.[emedicine.medscape.com] Porphyria Congenital Fiber Type Disproportion Congenital Fibrosis of the Extraocular Muscles Congenital Generalized Lipodystrophy Congenital Hepatic Fibrosis Congenital Hyperinsulinism[pastebin.com]

  • Hepatoerythropoietic Porphyria

    Short stature Generalized hypotonia Scoliosis Nystagmus Strabismus Failure to thrive Motor delay Muscular hypotonia Cryptorchidism Reduced bone mineral density Abnormal lung[mendelian.co] […] 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]

  • Kearns-Sayre Syndrome

    (ADP), Acute intermittent porphyria (AIP), Congenital erythopoietic porphyria (CEP), Erythropoietic protoporphyria (EPP), Hereditary coproporphyria (HCP) Porphyria cutanea[orphananesthesia.eu] […] features; onset: childhood-adulthood Slender build Facial muscle weakness; exertional dyspnea; obstructive sleep apnea; myopathy w/weakness, atrophy, exercise intolerance, myalgia[ncbi.nlm.nih.gov] […] type 2, acid alphaglucosidase (GAA) deficiency, GAA deficiency Porphyrie ( 1 Files ) Erkrankung: Porphyrie ICD 10: E80.0, E80.1, E80.2 Synonyme: ALA dehydratase deficiency porphyria[orphananesthesia.eu]

  • Meningeal Plague

    Initial signs and symptoms may be nonspecific with fever, chills, malaise, myalgia (muscular pain or tenderness), nausea, prostration, sore throat and headache.[ph.ucla.edu] Porphyria 赤血球生成性ポルフィリン症 PSYCHIATRIC DISORDERS 精神疾患 139.Delirium 譫妄 140.Bipolar Disorder 双極性障害 141.Eating Disorders 摂食障害 142.Factitious Disorder 虚偽性障害 143.Obsessive-Compulsive[igaku-shoin.co.jp] Signs and Symptoms: Infection causes febrile illness characterized by headache, myalgia, malaise, shaking chills, prostration, and gastrointestinal symptoms.[austincc.edu]

  • Benign Adult Familial Myoclonic Epilepsy

    (mostly on other seizure medications) and epileptic seizure type including primary-generalized, complex-partial or simple-partial seizures with motor component randomized[enotes.tripod.com] […] plaques MUTYH-related AFAP MUTYH-related attenuated familial adenomatous polyposis MUTYH-related attenuated familial polyposis coli MUTYH-related attenuated FAP MVA MVID Myalgia-eosinophilia[orpha.net] (ADP), Acute intermittent porphyria (AIP), Congenital erythopoietic porphyria (CEP), Erythropoietic protoporphyria (EPP), Hereditary coproporphyria (HCP) Porphyria cutanea[orphananesthesia.eu]

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