Create issue ticket

12 Possible Causes for Dizziness, Myoglobinuria after Exertion, Neonatal Hypoglycemia

  • Glycogen Storage Disease Type 1

    […] nodule Mitral regurgitation Hemiparesis Migraine Abnormality of exocrine pancreas physiology Gastrointestinal hemorrhage Anorexia Cranial nerve paralysis Aortic regurgitation Vertigo[mendelian.co] However, several cases of FBG have been detected through neonatal screening of galactose levels.[orpha.net] […] muscle fatigue, myalgia, muscle cramps, muscle swelling; myoglobinuria due to rhabdomyolysis may occur after exercise; severe myoglobinuria may lead to acute renal failure[clinicaladvisor.com]

  • Glycogen Storage Disease Type 3

    Older infants may also present with difficulty waking from sleep, poor growth, increased appetite, and dizziness.[encyclopedia.com] […] from hypoglycemia and accumulated glycogen, potentially improving the long-term health of children living in the eastern Hudson Bay region.[cmaj.ca] […] muscle fatigue, myalgia, muscle cramps, muscle swelling; myoglobinuria due to rhabdomyolysis may occur after exercise; severe myoglobinuria may lead to acute renal failure[clinicaladvisor.com]

  • Glycogen Storage Disease Type 4

    Older infants may also present with difficulty waking from sleep, poor growth, increased appetite, and dizziness.[encyclopedia.com] Myoglobinuria may occur after exercise[ 163 ].[wjgnet.com] Weakness and stiffness invariably appear in muscle groups subjected to vigorous or prolonged exertion. Upon ischemic exercise test, venous lactate fails to rise.[wjgnet.com]

  • Acute Exertional Rhabdomyolysis

    Overexertion combined with dehydration has many negative consequences that are well known to endurance athletes, with symptoms of muscle cramps, dizziness, and perhaps even[racereadycoaching.com] Phenotype The clinical phenotypes are very similar to VLCAD deficiency with three main forms: 1) fatal neonatal form presenting with dysmorphic features, severe skeletal and[ojrd.biomedcentral.com] Known triggering effects include fasting, fever and anti-inflammatory drugs. 5 The patient suffered myoglobinuria after performing prolonged physical exertions.[revistanefrologia.com]

  • Rhabdomyolysis

    Stiverne said he felt dizzy in the dressing room after the fight and was desperate for water.[sports.yahoo.com] Depending on the age at presentation (neonatal, childhood or adulthood), this disease has different clinical manifestations. ( 4 ) The neonatal-onset form manifests as liver[scielo.br] The development of an acute exertional rhabdomyolysis was confirmed by the increased serum enzyme levels and myoglobinuria.[casesjournal.biomedcentral.com]

  • Glycogen Storage Disease due to Phosphoglycerate Kinase 1 Deficiency

    Under such conditions pyruvate does not accumulate as it is converted to- a) Ethanol b) Lactic acid c) Acetyl co A d) Alanine e) Oxaloacetate. 5) A patient presents with dizziness[namrata.co] ABCC8 Diabetes mellitus, transient neonatal, Diabetes, permanent neonatal, Hyperinsulinemic hypoglycemia, Hypoglycemia, leucine-induced ABCD1 Adrenoleukodystrophy ABCD4 Methylmalonic[genda.com.ar] It usually presents with episodic cramps, weakness or myoglobinuria after exertion or prolonged exercise.[annalsofneurosciences.org]

  • Paroxysmal Rhabdomyolysis

    She did not have a urinary catheter, palpitations, dyspnea, back pain, abdominal pain, dysuria, or dizziness.[nejm.org] Phenotype The clinical phenotypes are very similar to VLCAD deficiency with three main forms: 1) fatal neonatal form presenting with dysmorphic features, severe skeletal and[ojrd.biomedcentral.com] Derstappen T, Mathias K, Losse B (1995) Complications of an idiopahic rhabdomyolysis (Meyer-Betz syndrome) after physical exertion.[link.springer.com]

  • Polyglucosan Body Myopathy Type 2

    , see Ménière disease AUH defect, see 3-methylglutaconyl-CoA hydratase deficiency aural vertigo, see Ménière disease auricular fibrillation, see familial atrial fibrillation[mygenomics.com] Clinical Presentation  Neonate-hypoglycemia, lactic acidosis.  Infancy- hepatomegaly, hypoglycemic seizures.  Doll like features-obesity, prominent cheeks, thin extremities[slideshare.net] It usually presents with episodic cramps, weakness or myoglobinuria after exertion or prolonged exercise.[annalsofneurosciences.org]

  • Carnitine Deficiency

    The cardiac muscle may also weaken, which can lead to fatigue, dizziness, chest pain and heart arrhythmia.[livestrong.com] hypoglycemia and sudden death JOURNAL-OF-CLINICAL-INVESTIGATION.[malattierare.regione.veneto.it] Known triggering effects include fasting, fever and anti-inflammatory drugs. 5 The patient suffered myoglobinuria after performing prolonged physical exertions.[revistanefrologia.com]

  • Genetic Recurrent Myoglobinuria

    Autonomic nervous system: heat and cold intolerance, temperature dysregulation, abnormal sweating, pallor, blotchiness, mottling of the skin with or without provocation, dizziness[sciencewerkedx.com] Phenotype The clinical phenotypes are very similar to VLCAD deficiency with three main forms: 1) fatal neonatal form presenting with dysmorphic features, severe skeletal and[ojrd.biomedcentral.com] Known triggering effects include fasting, fever and anti-inflammatory drugs. 5 The patient suffered myoglobinuria after performing prolonged physical exertions.[revistanefrologia.com]

Similar symptoms