Create issue ticket

2,078 Possible Causes for Fainting Spells, Neonatal Hypoglycemia, Subsarcolemmal Accumulation of Normal Mitochondria

  • Carnitine Transporter Deficiency

    hypoglycemia and sudden death JOURNAL-OF-CLINICAL-INVESTIGATION.[malattierare.regione.veneto.it] […] and intermyofibrillar accumulation of mitochondria in muscles ( mitochondria stain red).[amboss.com] Carnitine deficiency may cause muscle necrosis, myoglobinuria, lipid-storage myopathy, hypoglycemia, fatty liver, and hyperammonemia with muscle aches, fatigue, confusion,[msdmanuals.com]

  • Hypoglycemia

    Convert to ICD-10-CM : 775.6 converts approximately to: 2015/16 ICD-10-CM P70.4 Other neonatal hypoglycemia Clinical Information Hypoglycemia that occurs during the neonatal[icd9data.com] We present a case of an 85-year-old man who presented to the endocrinology clinic with symptoms of "fainting spells after large meals."[ncbi.nlm.nih.gov] Persistent hyperinsulinemic hypoglycemia of infancy Self-induced hyperinsulinemia Transitory neonatal hypoglycemia Tumor-induced hypoglycemia Clinical Information Syndrome[icd9data.com]

    Missing: Subsarcolemmal Accumulation of Normal Mitochondria
  • Addison's Disease

    spells sores in the mouth cravings for salt nausea vomiting irritability or depression If Addison’s disease goes untreated for too long, it can become an Addisonian crisis[healthline.com] […] weakness in the muscles fatigue and tiredness darkening in skin color weight loss or decreased appetite a decrease in heart rate or blood pressure low blood sugar levels fainting[healthline.com]

    Missing: Subsarcolemmal Accumulation of Normal Mitochondria
  • Hereditary Fructose Intolerance

    Fructose-1,6-diphosphate deficiency is another form of fructose intolerance, which usually presents as neonatal hypoglycemia.[healthhype.com] […] enzyme fructose-1-phosphate aldolase, cannot be converted into glucose, so it accumulates in liver, intestine, and kidneys, and inhibits glucose synthesis, thus causing hypoglycemia[healthhype.com]

    Missing: Subsarcolemmal Accumulation of Normal Mitochondria
  • Medium Chain Acyl CoA Dehydrogenase Deficiency

    Adverse events occurred in 5 children, 4 985A-- G homozygotes and 1 compound heterozygote with a very high initial octanoylcarnitine: 2 survived severe neonatal hypoglycemia[ncbi.nlm.nih.gov] Adverse events occurred in 5 children, 4 985A G homozygotes and 1 compound heterozygote with a very high initial octanoylcarnitine: 2 survived severe neonatal hypoglycemia[pediatrics.aappublications.org] Management strategies for neonatal hypoglycemia. J Pediatr Pharmacol Ther JPPT Off J PPAG. 2013;18(3):199-208. Harker HE, Emhardt JD, Hainline BE.[journals.sbmu.ac.ir]

    Missing: Subsarcolemmal Accumulation of Normal Mitochondria
  • Glycogen Storage Disease Type 6

    Patients with type 1 glycogen storage disease can present during the neonatal period with lactic acidosis and hypoglycemia.[themedicalbiochemistrypage.org] Hypoglycemia in hospitalized patients. Causes and outcomes. N Engl J Med 1986; 315 : 1245–1250. 43. Wolf AD, Lavine JE. Hepatomegaly in neonates and children.[nature.com]

    Missing: Subsarcolemmal Accumulation of Normal Mitochondria
  • Long Chain Hydroxyacyl-CoA Dehydrogenase Deficiency

    Seven (15%) of the patients presented in the neonatal period.[pediatrics.aappublications.org] It presents during infancy or early childhood, and is characterized by hypoketotic hypoglycemia, cardiomyopathy, hypotonia, and hepatomegaly.[cags.org.ae] Thirty-nine patients (78%) presented with hypoketotic hypoglycemia, the classical features of a fatty acid oxidation disorder.[pediatrics.aappublications.org]

    Missing: Subsarcolemmal Accumulation of Normal Mitochondria
  • Methylmalonic Acidemia

    Barkovich AJ, Ali F, Rowley HA et al (1998) Imaging patterns of neonatal hypoglycemia. AJNR 19:523–528 PubMed Google Scholar 30.[doi.org]

    Missing: Subsarcolemmal Accumulation of Normal Mitochondria
  • Maple Syrup Urine Disease

    The classic form presents in the first week of life with ketoacidosis, hypoglycemia, emesis, neonatal seizures, and hypertonia.[icd10data.com] , emesis, neonatal seizures, and hypertonia; the intermediate and intermittent forms present in childhood or later with acute episodes of ataxia and vomiting Applies To Disturbances[icd9data.com] Time: 4-5 weeks Preferred Specimen: 2-5 mL Blood - Lavender Top Tube Alternative Specimen: Oral Rinse (30-40 mL) Buccal Swabs Billing ICD Codes: 796.6 Abnormal findings on neonatal[genedx.com]

    Missing: Subsarcolemmal Accumulation of Normal Mitochondria
  • Nesidioblastosis

    Nesidioblastosis is the most common cause of neonatal hypoglycemia.[ncbi.nlm.nih.gov] I have been having episodes of faint spells, dizziness, and the shakes. I crave sugar when this happens.[healthboards.com] It is well recognized in the pediatric population as a frequent cause of persistent neonatal hypoglycemia.[ncbi.nlm.nih.gov]

    Missing: Subsarcolemmal Accumulation of Normal Mitochondria

Similar symptoms