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83 Possible Causes for Complete Blood Count Abnormal, Generalized Dystonia, Myopathy

  • Stiff-Person Syndrome

    Initial misdiagnoses included functional movement disorder (n   2), generalized dystonia and parkinsonism (n   1), and hereditary spastic paraparesis (n   1).[] ( G72.1 ) cramp and spasm ( R25.2 ) drug-induced myopathy ( G72.0 ) myalgia ( M79.1- ) stiff-man syndrome ( G25.82 ) Type 2 Excludes nontraumatic hematoma of muscle ( M79.81[] Prior diagnoses included psychogenic movement disorder (n   2), idiopathic generalized dystonia and parkinsonism (n   1), and hereditary spastic paraparesis (n   1).[]

  • Meige Syndrome

    The complete blood count, liver and kidney function tests, blood sugar, serum electrolytes, and thyroid function tests were normal.[] Deep brain stimulation of the globus pallidus internus (GPi DBS) is effective in the treatment of primary segmental and generalized dystonia.[] Deep brain stimulation for primary generalized dystonia: long-term outcomes. Arch Neurol 2009;66:465–470. 6. Jankovic J.[]

  • Influenza

    Previously described patients have suffered from acute-onset myoclonus and/or dystonia or post-viral parkinsonism.[] Immune-mediated necrotizing myopathy is a very rare inflammatory disease affecting skeletal muscles.[] Longer-term myalgias may be indicative of a metabolic myopathy, some nutritional deficiencies, or chronic fatigue syndrome.[]

  • Subacute Combined Degeneration of Spinal Cord

    Blood tests that may be ordered include: Complete blood count (CBC) Vitamin B12 blood level Methylmalonic acid blood level Vitamin B12 is given, usually by injection into[] Generalized dystonia (e.g., dystonia musculorum deformans) is an inherited condition in which persistent and often painful twisting and writhing movements of any muscle group[] Clinically, vitamin E deficiency causes a sensory peripheral neuropathy, ataxia, retinitis pigmentosa, and skeletal and cardiac myopathy.[]

  • Thiamine Deficiency

    For all 33 patients, complete blood counts and blood chemistries processed on admission were normal. Some cases had evidence of hepatic and renal abnormalities.[] Most commonly BTBGD is characterized by recurrent subacute onset of encephalopathy manifest as confusion, generalized seizures, ataxia, dystonia, supranuclear facial palsy[] The younger brother presented aged 19 years with a myopathy (patient 2, now 35 years old).[]

  • MELAS Syndrome

    Complete blood count, electrolyte levels, liver function tests, blood urea nitrogen, and creatinine levels were all normal. Serum glucose was elevated.[] ; alternating with ataxia, dystonia, choreoathetosis and spastic paraplegia.[] Abstract Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome is a rare neurodegenerative disease caused by the decreased ability[]

  • Myxedema

    […] swelling Macroglossia Ptosis Periorbital edema Coarse, sparse hair Nonpitting edema TABLE 2 Physical Findings in Myxedema Coma Altered mentation Alopecia Bladder dystonia[] This hypertrophic myopathy may impair ability to dilate the upper airway. The hypothyroidism induced myopathy is known to affect proximal limb muscles.[] The pathogenesis of thyroid myopathy is still not well understood. Isolated serum CK elevation is the most common abnormality.[]

  • Congenital Acquired Immune Deficiency Syndrome

    Blood tests, including a complete blood count (CBC), are done.[] Generalized dystonia (e.g., dystonia musculorum deformans) is an inherited condition in which persistent and often painful twisting and writhing movements of any muscle group[] […] associated with acquired immunodeficiency syndrome (disorder) Cryptosporidiosis associated with acquired immunodeficiency syndrome (disorder) Human immunodeficiency virus myopathy[]

  • Granulomatosis with Polyangiitis

    These tests may include: Complete blood count (CBC) to look for: Evidence of anemia (common in Granulomatosis with polyangiitis (Wegener's)) Abnormal white blood cell count[] 0001332 Epileptic encephalopathy 0200134 Generalized myoclonic seizures 0002123 Hyperreflexia Increased reflexes 0001347 Hypertonia 0001276 Intellectual disability Mental[] […] junction والعضلات Myasthenia gravis - Muscular dystrophy - Myotonic dystrophy - Myotonia congenita - Thomsen disease - Neuromyotonia - Paramyotonia congenita - Centronuclear myopathy[]

  • McLeod Neuroacanthocytosis Syndrome

    The routine investigations, complete blood count, renal function tests, liver function tests, serum electrolytes, HIV ELISA, 24 hour urinary copper and serum cerruloplasmin[] Clincial features include chorea, oromandibular dystonia (which may be mutilating) or generalized dystonia, phonic tics, feeding/ tongue protrusion dystonia, head drops, ‘[] McLeod myopathy revisited – more neurogenic and less benign.[]

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