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136 Possible Causes for Erythrocyte Sedimentation Rate Abnormal, Muscular Atrophy

  • Enthesitis-Related Arthritis

    For example, inflammatory markers such as erythrocyte sedimentation rate (ESR), C-reactive protein (CRP) may be elevated.[] Three patients (6.1%) had severe muscular atrophy. Four (8.2%) patients had growth failure; pubertal delay was seen in 2 (4.1%).[] sedimentation rate C-reactive protein Liver enzymes HLA-B27 marker Other important markers of inflammation Note that this disease is not associated with specific lab results[]

  • African Trypanosomiasis

    Treatment for human African trypanosomiasis is dependent on the species of trypanosome causing the disease and the stage of the disease (stage 1 defined by parasites being present in blood and lymphatics whilst for stage 2, parasites are found beyond the blood-brain barrier in the cerebrospinal fluid (CSF)).[…][]

  • Hemophilia

    Inhibitor development is one of the major problems in hemophilia patients. Whereas the inhibitor incidence in hemophilia A is estimated to be as high as 25-30%, it appears to be less frequent in hemophilia B, occurring in about 1-3% of hemophilia B patients. There are only a few case reports about immune tolerance[…][]

  • Hemophilia B

    Disseminated mycobacterial infection was found at autopsy in a male patient with hemophilia B and acquired immunodeficiency syndrome (AIDS). In May 1986, 23 months before death, the patient had encephalitis for one month and in July he developed a fever, malaise and generalized lymphoadenopathy. Human[…][]

  • Chronic Pancreatitis

    sedimentation rate Abnormality may indicate autoimmune pancreatitis 10 Laboratory Testing .[] The following genes are required for Invitae carrier screening and will be added to your order, CFTR (cystic fibrosis), SMN1 (spinal muscular atrophy), FMR1 (fragile X syndrome[] sedimentation rate Abnormality may indicate autoimmune pancreatitis 10 Table 3 Laboratory Tests Used in the Evaluation of the Patient with Suspected Chronic Pancreatitis[]

  • Multicentric Castleman's Disease

    Laboratory abnormalities: anemia, thrombocytopenia or thrombocytosis, elevated C-reactive protein, Westergren erythrocyte sedimentation rate, fibrinogen, hypergammaglobulinemia[] atrophy type Imaizumi Okinawa type Neuropathy Hereditary motor and sensory neoplasia congenital neutropenia Muscular atrophy adult spinal Imaizumi Kuroki syndrome Craniosynostosis[] (elevated erythrocyte sedimentation rate, hypergammaglobulinemia or hypoalbuminemia).[]

  • Familial Cold Urticaria

    Ice-cube tests and P-K tests were negative, and laboratory studies were remarkable only for a rise in leukocytes and erythrocytic sedimentation rate after positive challenge[] The following genes are required for Invitae carrier screening and will be added to your order, CFTR (cystic fibrosis), SMN1 (spinal muscular atrophy), FMR1 (fragile X syndrome[] Abnormal serum proteins were not found.[]

  • Congenital Clubbing of the Fingers

    sedimentation rate and abnormality of plasma viscosity R70.0 Elevated erythrocyte sedimentation rate R70.1 Abnormal plasma viscosity Reimbursement claims with a date of service[] The clinical application of preimplantation genetic diagnosis for the patient affected by congenital contractural arachnodactyly and spinal and bulbar muscular atrophy.[] R68.3 Clubbing of fingers R68.8 Other general symptoms and signs R68.83 Chills (without fever) R68.89 Other general symptoms and signs R69 Illness, unspecified R70 Elevated erythrocyte[]

  • CINCA Syndrome

    rate Abnormal facial features can sometimes be seen What causes NOMID/CINCA?[] Spinal muscular atrophy, distal, autosomal recessive, 2; ?[] Disruption of nongenomic testosterone signaling in a model of spinal and bulbar muscular atrophy. Mol Endocrinol . 2012 Jul. 26(7):1102-16. [Medline] .[]

  • Dermatomyositis

    Inflammatory markers (erythrocyte sedimentation rate and CRP) may/may not be abnormal despite active disease. The diagnosis of JDM needs strong clinical suspicion.[] atrophy).[] MDA addresses the muscular dystrophies, spinal muscular atrophy, ALS, Charcot-Marie-Tooth disease, myasthenia gravis, Friedreich's ataxia, metabolic diseases of muscle, and[]

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