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203 Possible Causes for Anemia, Mild Facial Muscle Weakness

  • Orthostatic Hypotension

    The case of a patient who developed aseptic meningitis, hemolytic anemia, hepatitis, and orthostatic hypotension simultaneously during treatment with trimethoprim-sulfamethoxazole[ncbi.nlm.nih.gov] […] findings in some affected individuals: Arched palate Hyperextensible joints Sluggish deep-tendon reflexes Mild facial-muscle weakness Hypotonic skeletal muscles Findings[ncbi.nlm.nih.gov] Although previous reports have shown that the mechanism by which erythropoietin improves orthostatic hypotension is related to improvement in anemia, other mechanisms may[ncbi.nlm.nih.gov]

  • Subacute Combined Degeneration of Spinal Cord

    […] response in a fourth patient with mild pernicious anemia but severe subacute combined degeneration of the spinal cord. 3.[bloodjournal.org] Less commonly, muscle weakness occurs in specific patterns—for example, involving only the facial, shoulder, or calf muscles—and the progress of the disease is much slower[britannica.com] This is what leads to megaloblastic anemia.[symptoma.com]

  • Polymyositis

    No history of (or current) autoimmune hemolytic anemia. No current anticoagulant therapy.[clinicaltrials.gov] Facial muscles are unaffected in PM and DM, but mild facial muscle weakness is common in patients with IBM.[accessmedicine.mhmedical.com] Rituximab was stopped; peripheral blood smear revealed schistocytes with anemia and thrombocytopenia suggestive of TTP.[annalsofian.org]

  • Congenital Acquired Immune Deficiency Syndrome

    The neonate had mild anemia but no other signs of congenital CMV infection.[experts.umn.edu] Less commonly, muscle weakness occurs in specific patterns—for example, involving only the facial, shoulder, or calf muscles—and the progress of the disease is much slower[britannica.com] Hepatitis Nephropathy Persistent fever lasting more than one month Neutropenia ( 1,000/µL), thrombocytopenia ( 100,000/µL) or anemia ( 8 g/dL).[symptoma.com]

  • Congenital Muscular Dystrophy

    A CELLULE FALCIFORMI ANEMIA CONGENITA DISERITROPOIETICA ANEMIA DI FANCONI ANEMIA SIDEROBLASTICA ANGELMAN SINDROME DI ANGIOEDEMA DI QUINCK ANGIOMA ANOMALIA MITRALICA CONGENITA[birdfoundation.org] Atrophy and weakness of facial muscles, ptosis, and frontal baldness produce a characteristic facial appearance.[neuropathology-web.org] AGAMMAGLOBULINEMIA AICARDI SINDROME DI ALBRIGHT MALATTIA DI ALFA1-ANTITRIPSINA (AAT) DEFICIT DI ALKAPTONURIA ALLERGIE ALZHEIMER MORBO DI AMILOIDOSI ANCORAGGIO MIDOLLARE ANEMIA[birdfoundation.org]

  • Bloom Syndrome

    The Fanconi's anemia complementation group C gene was mapped to chromosome 9q22.3, but its product function is not sufficiently clear.[ncbi.nlm.nih.gov] ., shoulders, elbows, hips, knees, ankles), clinodactyly, and evidence of mild but generalized muscle weakness.[accessanesthesiology.mhmedical.com] Interestingly, one of the complexes, termed BRAFT, also contains five of the Fanconi anemia (FA) complementation group proteins (FA proteins).[ncbi.nlm.nih.gov]

  • Stiff-Person Syndrome

    It is frequently associated with other autoimmune diseases such as diabetes, thyroiditis, vitiligo, and pernicious anemia.[ninds.nih.gov] In later stages of SPS, mild atrophy and muscle weakness are likely.[mdedge.com] This case report describes stiff-person syndrome in association with pernicious anemia and diabetes mellitus.[ncbi.nlm.nih.gov]

  • Platelet-Type Bleeding Disorder 19

    Related phenotypes are anemia and spontaneous hematomas UniProtKB/Swiss-Prot : 76 Bleeding disorder, platelet-type 19: A disorder characterized by increased bleeding tendency[malacards.org] Systemic Features: Mild facial muscle weakness may be apparent.[disorders.eyes.arizona.edu] At least 40% of affected individuals also develop one or more autoimmune conditions, including hemolytic anemia, immune thrombocytopenic purpura, immune-mediated neutropenia[centogene.com]

  • Carcinoma of the Prostate

    Microangiopathic hemolytic anemia associated with cancers. Symptomatic treatment by plasma exchange. Ann Med interne (Paris), 145 (1994), pp. 365-368 [4] V.[htct.com.br] The patient had oral candidiasis, thin skin, multiple petechiae on the chest, a small supraclavicular fat pad and proximal muscle weakness.[ec.bioscientifica.com] The evolution at the end of two months is marked by the occurrence of repeated anemias requiring several transfusions with erythrocyte pellets, then the patient’s death.[scirp.org]

  • Brandt Syndrome

    Other features associated with severe and chronic zinc deficiency include failure to thrive, mental slowness, photophobia, hypogeusia, anemia, poor wound healing, hypogonadism[orpha.net] . • The syndrome can cause intellectual disability, a characteristic facial appearance and weak muscle tone in infancy.[timesfreepress.com] It presents as erythematous skin lesions, hyperglucagonemia, diabetes mellitus, anemia, weight loss, glossitis, cheilitis, neuropsychiatric disturbances, steatorrhea and diarrhea[explainmedicine.com]

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