Create issue ticket

245 Possible Causes for Ketonuria, Pediatric Disorder

  • Methylmalonic Acidemia

    Department of Pediatric Metabolic Disorders Tehran University of Medical Sciences Tehran Iran 3.[link.springer.com] Laboratory analysis showed hyperglycemia with acidosis and ketonuria. She was treated with parenteral fluid, electrolyte, and insulin infusion.[ncbi.nlm.nih.gov] All patients had previous episodes of metabolic acidosis, lactic acidemia, ketonuria, and hyperammonemia.[ncbi.nlm.nih.gov]

  • Isovaleric Acidemia

    In contrast to an untreated older sister with the same disorder, the treated infant has had fewer periods of acidosis and has manifested normal psychomotor development.[pediatrics.aappublications.org] Hyperglycemia, ketonemia, ketonuria and metabolic acidosis are the main clinical features of diabetic ketoacidosis (DKA) and these same symptoms can also be seen in acute[ncbi.nlm.nih.gov] At admission, he had vomiting associated with dehydration, acidosis, ketonuria, coma and a pungent, rather unpleasant odor.[ncbi.nlm.nih.gov]

  • Propionic Acidemia

    She is a member of the Academy of Nutrition and Dietetics, the Pediatric Nutrition Practice Group and the Society for Inherited Metabolic Disorders (SIMD) and serves on the[books.google.ro] […] presented, paying special attention to the early symptoms of this disease, such as increased drowsiness, muscular hypotonia, poor feeding, hypothermia, metabolic acidosis, ketonuria[ncbi.nlm.nih.gov] It is frequently accompanied by metabolic acidosis with anion gap, ketonuria, hypoglycemia, hyperammonemia, and cytopenias.[ncbi.nlm.nih.gov]

  • Diabetic Ketotic Coma

    You’ll benefit from unique, global perspectives on adult and pediatric endocrinology prepared by an international team of renowned authorities.[books.google.com] Because of a preferential increase in 3-OHBA, ketonuria seemed to be absent in the regular nitroprusside test.[ncbi.nlm.nih.gov] Special considerations in hypoglycemic patients include alcohol abuse, the pediatric population, and conditions involving no IV access.[ahcmedia.com]

  • Acute Alcohol Intoxication

    The inactive ALDH2(2) allele is dominant , J Clin Invest , 1989 , vol. 83 (pg. 314 - 6 ) Diagnostic and Statistical Manual of Mental Disorders , 2000 4th ed Washington, DC[academic.oup.com] Urinalysis and urine toxicology for the presence of opiates and cocaine metabolites, ketonuria or evidence of infection.[clinicaladvisor.com] American Psychiatry Association Text Revision Estimated blood alcohol concentrations for child and adolescent drinking and their implications for screening instruments , Pediatrics[academic.oup.com]

  • Glycogen Storage Disease Type 1

    Nelson Textbook of Pediatrics. 16th ed. Philadelphia: Saunders; 2000. p. 405. 6. Bickel H, Manz F.[journalofpediatriccriticalcare.com] Laboratory findings are fasting hypoglycemia and ketonuria, hyperglycemia and hypergalactosemia in the postabsorptive state, hypercholesterolemia and hyper-lipidemia, moderately[wjgnet.com] […] patients with inheritable metabolic disorders.[ojrd.biomedcentral.com]

  • Fructose-1,6-Diphosphatase Deficiency

    Disorders E-2903 168 Measurement of Health Outcomes in Pediatric Neurologic Disorders E-2910 169 The Influence of Computer Resources on Child Neurology E-2918 170 Education[books.google.de] Fructose-1,6-diphosphatase (FDPase) deficiency is characterized by episodes of lactic acidemia, hypoglycemia, and ketonuria.[ncbi.nlm.nih.gov] They presented with ketonuria, elevated plasma transaminase activity and severe metabolic acidosis during hypoglycaemic crises, which resembled Reye syndrome.[ncbi.nlm.nih.gov]

  • Russell-Silver Syndrome

    Written by distinguished authorities, this volume is a comprehensive text on the mechanisms, diagnosis, and management of pediatric endocrine disorders.[books.google.com] Ketonemia and ketonuria normally precede hypoglycemia.[magicfoundation.org] Disorders of growth hormone/insulin-like growth factor secretion and action. In: Sperling MA, ed. Pediatric Endocrinology . 4th ed.[stlukes-stl.com]

  • Hyperammonemia

    Pediatrics 2002;109;150-152 Enns, GM. Neurologic Damage and Neurocognitive Dysfunction in Urea Cycle Disorders. Semin Pediatr Neurol 15:132–139 Gropman A, Rigas A.[nucdf.org] It is frequently accompanied by metabolic acidosis with anion gap, ketonuria, hypoglycemia, hyperammonemia, and cytopenias.[ncbi.nlm.nih.gov] Urea cycle disorders are an important and treatable cause of hyperammonemia in the newborn and pediatric age group.[ncbi.nlm.nih.gov]

  • Multiple Carboxylase Deficiency

    Disorders E-2903 168 Measurement of Health Outcomes in Pediatric Neurologic Disorders E-2910 169 The Influence of Computer Resources on Child Neurology E-2918 170 Education[books.google.com] Clinical considerations: Poor feeding, vomiting, lethargy, tachypnea Ketonuria Metabolic ketoacidosis Hyperammonemia Hypoglycemia Referral: If signs are present or infant[archildrens.org] Provide emergency treatment/referral for signs/symptoms of hypoglycemia, metabolic acidosis, ketonuria, or seizures.[medicalhomeportal.org]

Further symptoms

Similar symptoms