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113 Possible Causes for Erythropoietic Porphyria, Hyponatremia, 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] Hyponatremia-associated rhabdomyolysis. Nephron. 1999;82(3):274-7. [8] 6- Rizzieri DA. Rhabdomyolysis after correction of hyponatremia due to psychogenic polydipsia.[revistanefrologia.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] Computed tomography was unremarkable, and blood tests demonstrated hyponatremia, acute kidney injury, and a neutrophilic leukocytosis.[ncbi.nlm.nih.gov] Severe hyponatremia, urine that develops orange colour on exposure to light and gastrointestinal symptom combination with neurologic symptoms are three valuable clues that[ncbi.nlm.nih.gov]

  • Acute Intermittent Porphyria

    Neurovisceral symptoms resolved, and severe hyponatremia was corrected with IV saline solution without complications.[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] There are seven main types of porphyrias; acute intermittent porphyria and plumboporphyria are predominantly neuropsychiatric; congenital erythropoietic porphyria, porphyria[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] Another important early sign of this disorder is hyponatremia.[hematologyandoncology.net] Molecular genetics of congenital erythropoietic porphyria.[ncbi.nlm.nih.gov]

  • 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] Serum sodium concentration should be checked in patients during attacks, since hyponatremia a quite common symptom.[symptoma.com] 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]

  • Acute Porphyria

    Called also intermittent acute porphyria. congenital erythropoietic porphyria (CEP) a form of erythropoietic porphyria, with cutaneous photosensitivity leading to mutilating[medical-dictionary.thefreedictionary.com] The hyponatremia and elevation of creatine kinase improved [Table 1].[mjdrdypu.org] 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

    Hypokalemia and hyponatremia in the setting of laxative and diuretic misuse/abuse.[sites.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] 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]

  • Hepatoerythropoietic Porphyria

    Hypomagnesemia - Ca 2 Hypercalcaemia / Hypocalcaemia / Disorders of calcium metabolism Fluid, electrolyte and acid-base balance Electrolyte disturbance - Na Hypernatremia / Hyponatremia[wikidoc.org] […] 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]

  • 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] Laboratory investigation revealed elevated blood urea nitrogen and creatinine level, hypocalcemia, hyperphosphatemia, and hyponatremia.[ncbi.nlm.nih.gov] […] 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]

  • 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] The author is aware of at least 3 patients whose clinical course deteriorated during the first three days of therapy with CaNa 2 EDTA chelation and in whom severe hyponatremia[emedicine.medscape.com] Linear regression analysis showed log of BLL was significantly associated with abdominal pain, myalgia and anorexia.[ncbi.nlm.nih.gov]

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