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62 Possible Causes for Hyperactive Deep Tendon Reflexes, Hypokalemia

  • Hypomagnesemia

    Hypokalemia events were related to malnutrition (odds ratio, 2.79; 95% confidence interval, 1.09-7.14; P .045).[] deep tendon reflexes Chvostek's and Trousseau's signs Nystagmus Ataxia Cardiac arrhythmia Diagnostic Test Results-Laboratory Serum magnesium level is less than 1.5 mEq/L.[] deep tendon reflexes Chvostek's and Trousseau's signs Nystagmus Ataxia Cardiac arrhythmia Hypomagnesemia Diagnostic Test Results-Laboratory Serum magnesium level is less[]

  • Paraparesis

    The condition needs to be considered in the differential diagnosis of neuromuscular weakness in the context of hypokalemia by the treating physicians.[] deep-tendon reflexes in the lower limbs.[] We present a case of TPP in a 19-year male with rapidly progressive paraparesis & hypokalemia.[]

  • Hypocalcemia

    The patient improved with cessation of drugs and appropriate management of hypocalcemia and hypokalemia with calcium, vitamin D, magnesium, and potassium replacement.[] Manifestations include hyperactive deep tendon reflexes, Chvostek's sign, muscle and abdominal cramps, and carpopedal spasm.[] ‘Other conditions that may prolong QT intervals are clinical hypocalcemia, hypokalemia, ischemia, or infarction.’[]

  • Electrolyte Imbalance

    Here, we present a case of a heart donor with severe electrolyte imbalance, specifically severe hypokalemia, and severe hypernatremia.[] deep tendon reflexes.[] […] hypomagnesemia t widened hypercalcemia t tall hyperkalemia hypomagnesemia t inverted hypokalemia shallow, flat u prominent hypokalemia Quote from fa2z thank you very much[]

  • Hypermagnesemia

    We present a 44-year-old white man referred for hypokalemia. Clinical evaluation was unremarkable.[] Signs and symptoms include muscle tremors and weakness, athetoid movements (continuous, slow, involuntary twisting/writhing movements), ataxia, and hyperactive deep tendon[] Physical examination revealed 3/5 muscle strength in the right extremities and 4-/5 in the left extremities with diffusely hyporeflexic deep tendon reflexes.[]

  • Hypokalemia

    External links [ edit ] Low potassium (hypokalemia) Low Potassium (Hypokalemia) Low Potassium (Hypokalemia) Content of[] On the first post-operative day, her physical exam reveals hyperactive deep tendon reflexes. Which of the following electrolyte abnormalities is most likely present?[] Hypokalemia is a common clinical disorder caused by a variety of different mechanisms.[]

  • Chromosome 17p13.1 Deletion Syndrome

    September 27, 2018 by Peter Ciszewski Hypokalemic periodic paralysis (HOKPP) is characterized by episodes of muscle paralysis associated with a fall in blood potassium levels (hypokalemia[] deep tendon reflexes 0006801 Inverted nipples 0003186 Joint laxity Joint instability Lax joints Loose-jointedness Loosejointedness [ more ] 0001388 Knee flexion contracture[] deep tendon reflexes 10% Contiguous gene syndrome 10% Long hallux 10% Craniosynostosis 10% Bilateral single transverse palmar creases 10% Choanal atresia 10% Holoprosencephaly[]

  • Electrolytes Abnormal

    Hyperkalemia Several concepts in hypokalemia are relevant to hyperkalemia.[] deep tendon reflexes, dysrhythmias, mood changes, confusion, reduced motility with anorexia, nausea, constipation and distention.[] […] moderate hypokalemia.[]

  • Ocular Albinism with Congenital Sensorineural Deafness

    […] hormone level Immune System Recurrent candida infections Recurrent vulvovaginal candidiasis Digestive System Hepatosplenomegaly Feeding difficulties Metabolism/homeostasis Hypokalemia[] deep tendon reflexes Hypopigmentation of hair Telecanthus Abnormal conjugate eye movement Clumsiness Abnormality of skin pigmentation Diffuse cerebellar atrophy Limb dysmetria[] Skeletal muscle atrophy Hypopigmentation of the fundus Red hair Abnormal anterior chamber morphology White eyelashes Scoliosis Gaze-evoked horizontal nystagmus Late onset Hyperactive[]

  • Familial Primary Hypomagnesemia with Normocalciuria and Normocalcemia

    In patients with FXYD2 mutations, no hypokalemia or metabolic alkalosis is observed. In contrast, in patients with HNF1B mutations, hypokalemia can be detected.[] deep tendon reflexes 59 32 frequent (33%) Frequent (79-30%) HP:0006801 11 moderate global developmental delay 59 32 frequent (33%) Frequent (79-30%) HP:0011343 12 microcephaly[] Studies on the pathogenesis of hypokalemia in Gitelman's syndrome: role of bicarbonaturia and hypomagnesemia. Am J Nephrol . 1998. 18(1):42-9. [Medline] .[]

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