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114 Possible Causes for Dark Urine, Erythropoietic Porphyria, Myalgia

  • Acute Hepatic Porphyria

    Muscle weakness, tremor, diaphoresis, dysuria, dark urine, bladder distension and severe neuropathy may be encountered as well, and a missed diagnosis may lead to severe and[] 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[] Possibly or definitely related AEs reported in two or more cases were injection site reactions and myalgia; all of these events were mild.[]

  • Porphyria

    Signs and Symptoms Diagnosis Treatment Symptoms vary depending on the type of porphyria, but some of the more common include: Dark urine Skin sensitivity, including blistering[] Desnick, Congenital erythropoietic porphyria: Recent advances, Molecular Genetics and Metabolism, 10.1016/j.ymgme.2018.12.008, (2018).[] urine AR, autosomal recessive; XL, X-linked Pathophysiology Heterogenous group of inherited or acquired disorders of heme biosynthesis Partial deficiency of 1 of 7 enzymes[]

  • Acute Intermittent Porphyria

    A 47-year-old man presented with abdominal pain, neck stiffness, severe transient hypertension and unusually dark urine.[] There are seven main types of porphyrias; acute intermittent porphyria and plumboporphyria are predominantly neuropsychiatric; congenital erythropoietic porphyria, 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.[]

  • Erythropoietic Coproporphyria

    Uroporphyrin I and III; Dark urine is passed from birth Coproporphyrin I and III Protoporphyrin Hereditary Coproporphyria (HCP) Hepatic; Autosomal dominant; Young adulthood[] Prenatal exclusion of congenital erythropoietic porphyria (Günther's disease) in a fetus at risk. Hum. Genet. 53 (1980) 217–221 Google Scholar Doss, M.[] […] reddish urine 64 Dark/reddish urine 55 Sores/crusting 50 Muscular pain 63 Abnormal hair growth 33 Blisters 32 Muscular weakness 59 Increased pigmentation 30 Palpitations[]

  • Hereditary Coproporphyria

    The patient showed dark urine, complained of hair loss and took since 1994 a hormonal oral contraceptive. No photosensitivity was observed.[] From her mother she inherited the trait of hereditary coproporphyria; from both parents she inherited the trait of congenital erythropoietic porphyria (Günther disease).[] Neurological manifestations can affect the central nervous system as much as the peripheral nervous system (myalgia, paresis, ascending flaccid paralysis of the limbs, or[]

  • Myoadenylate Deaminase Deficiency

    Urine 526 Case 84 A Woman with Progressive Proximal Muscle Weakness 533 Case 85 A Sedentary Man with Acute Respiratory Failure and Myoglobinuria 539 Case 86 A Uremic Man[] 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[] A diagnosis of tension myalgia or myofascial-type pain is often considered when no objective findings are seen in the evaluation.[]

  • Hepatoerythropoietic Porphyria

    urine) Familial Mediterranean fever Best Tests Subscription Required Therapy Subscription Required References Subscription Required Last Reviewed: 03/09/2017 Last Updated[] Erythropoietic porphyrias include erythropoietic protoporphyria and congenital erythropoietic porphyria.[] […] paralysis Urinary retention Abnormal urinary color Psychotic episodes Hypertensive crisis Elevated urinary delta-aminolevulinic acid Paralytic ileus Micrognathia Focal seizures Myalgia[]

  • Extrahepatic Cholestasis

    The biochemical derangement is reinforced by clinical symptoms and signs: pale stool - no bilirubin reaching gastrointestinal tract for conversion to stercobilin dark orange[] ., thalassemia, pernicious anemia, erythropoietic porphyria, and sideroblastic anemia ) Resolving hematoma or internal hemorrhage (e.g., in trauma patients or postsurgical[] A trial of corticosteroids in patients with idiopathic granulomatous hepatitis who are symptomatic, with fever, myalgias, and arthralgias, may be helpful.[]

  • Toxic Hepatitis

    Four weeks later; he developed dark urine and pale stools, associated with asthenia and right hypochondrial pain.[] Can J Physiol Pharmacol 1987; 65: 1762–79Gelman, S Gross U, Hoffman GF, Doss MO: Erythropoietic and hepatic porphyrias.[] […] inhibition of mitochondrial DNA polymerase γ by fialuridine and its metabolites. 9 Mechanisms of idiosyncratic adverse drug reactions Pharmaceutical variation—eosinophilia-myalgia[]

  • Primary Hyperoxaluria

    CASE 3: A 2.5-year-old girl had attacks of dark urine without any pain; renal stones were imaged on sonography.[] Lipase Deficiency Congenital Erythropoietic Porphyria; UROS mutation: c.331G A Glycogen Storage Disease Type IV Mucopolysaccharidosis Type I (MPS I) Mucopolysaccharidosis[] […] joints, the retina, and the central nervous system, causing complications in the form of cardiomyopathy, disturbances in the cardiac conduction system, retinopathy, severe myalgia[]

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