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54 Possible Causes for Complete Blood Count Abnormal, 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[] Possibly or definitely related AEs reported in two or more cases were injection site reactions and myalgia; all of these events were mild.[] Four patients were assessed as having AEs possibly related to study drug, including injection site reaction (mild and self-limiting), hypersensitivity, myalgia, headache,[]

  • Porphyria

    Desnick, Congenital erythropoietic porphyria: Recent advances, Molecular Genetics and Metabolism, 10.1016/j.ymgme.2018.12.008, (2018).[] What is congenital erythropoietic porphyria?[] Erythropoietic porphyrias include erythropoietic protoporphyria and congenital erythropoietic porphyria.[]

  • Acute Intermittent Porphyria

    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.[] Neurological manifestations can affect the central nervous system as much as the peripheral nervous system (myalgia, paresis, ascending flaccid paralysis of the limbs, or[]

  • 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.[] Molecular genetics of congenital erythropoietic porphyria.[] From her mother she inherited the trait of hereditary coproporphyria; from both parents she inherited the trait of congenital erythropoietic porphyria (Günther disease).[]

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

  • Hepatoerythropoietic Porphyria

    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[] Certain clinical and biochemical features distinguish HEP from erythropoietic porphyria and erythropoietic protoporphyria, the two diseases with which HEP is often confused[]

  • Anemia

    Often, anemia caused by chronic diseases goes undetected until a routine test such as a complete blood count (CBC) reveals abnormal results.[] Metabolic correction of congenital erythropoietic porphyria with iPSCs free of reprogramming factors. Am. J. Hum. Genet. 91, 109–121 (2012). 104.[] Empiric use of steroids prior to retreatment may diminish minor reactions that occur the next day. 62 Patients may also experience self-limited arthralgia, myalgias, and/or[]

  • Thrombocytopenia

    In a patient who is otherwise in his/her usual state of good health who has not taken a new medication, has thrombocytopenia and no other abnormality found in a complete blood[] When the spleen bleeds following physical trauma Following spontaneous rupture For long-term treatment of congenital erythropoietic porphyria (CEP) if severe hemolytic anemia[] CASE PRESENTATION: We report a 65-year old lady who was admitted in a Tertiary Care Center in the state of Kerala in India, with 7 day history of fever, myalgia and reduced[]

  • Sideroblastic Anemia

    Complete blood count with differential will show variable severity of anemia, with usually normal leukocytes and platelets.[] Congenital erythropoietic porphyria (CEP), an autosomal recessive disorder, results from the markedly deficient activity of uroporphyrinogen III synthase [UROS] (also known[] […] features; onset: childhood-adulthood Slender build Facial muscle weakness; exertional dyspnea; obstructive sleep apnea; myopathy w/weakness, atrophy, exercise intolerance, myalgia[]

  • Urticaria

    Dominantly inherited cutaneous and neurocutaneous porphyrias ( porphyria cutanea tarda, hereditary coproporphyria, variegate porphyria and erythropoietic protoporphyria )[] […] to increased activity of kinins. 2 It is speculated that interleukin 1 (IL-1) is released on the skin exposed to pressure, and it would be responsible for fever, malaise, myalgia[] […] inflammation of the anterior eye, uveitis, periorbital oedema, serositis, stomatitis, ulcers, meningeal inflammation leading to headaches, abdominal complaints, arthralgia, myalgia[]

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