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225 Possible Causes for Ketonuria, Pediatric Disorder

  • 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[] American Psychiatry Association Text Revision Estimated blood alcohol concentrations for child and adolescent drinking and their implications for screening instruments , Pediatrics[]

  • Diabetic Ketotic Coma

    You’ll benefit from unique, global perspectives on adult and pediatric endocrinology prepared by an international team of renowned authorities.[] Because of a preferential increase in 3-OHBA, ketonuria seemed to be absent in the regular nitroprusside test.[] Often 50 mmol/L - no detectable ketonuria or acidosis - hypernatraemia (may be hypo-) - uraemia - /- respiratory alkalosis - increased osmolality Differential diagnosis -[]

  • Anorexia Nervosa

    Identifying and treating eating disorders. Pediatrics. 2003;111:204-11. ).[] Eating disorders. Indian J Pediatr, 1998; 65(4): 487-94. Lewinsohn PM, Striegel-Moore RH, Seeley JR.[] Finally, he was diagnosed with early-onset anorexia nervosa and anxiety disorder based on the Diagnostic and Statistical Manual of Mental Disorders 5. the case highlights[]

  • Isovaleric Acidemia

    , Hospital de Cruces, Group of Metabolism, Biocruces Health Research Institute, Barakaldo, Spain. 3 Metabolic Disorders, Dietetics and Nutrition Unit, Virgen del Rocío University[] 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[] At admission, he had vomiting associated with dehydration, acidosis, ketonuria, coma and a pungent, rather unpleasant odor.[]

  • Methylmalonic Acidemia

    Department of Pediatric Metabolic Disorders Tehran University of Medical Sciences Tehran Iran 3.[] Laboratory analysis showed hyperglycemia with acidosis and ketonuria. She was treated with parenteral fluid, electrolyte, and insulin infusion.[] Biochemically, the disorder is typically characterized by: metabolic acidosis, ketonemia or ketonuria, hyperammonemia, leukopenia, thrombocytopenia and anemia.[]

  • 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[] […] presented, paying special attention to the early symptoms of this disease, such as increased drowsiness, muscular hypotonia, poor feeding, hypothermia, metabolic acidosis, ketonuria[] It is frequently accompanied by metabolic acidosis with anion gap, ketonuria, hypoglycemia, hyperammonemia, and cytopenias.[]

  • Glycogen Storage Disease Type 1

    Nelson Textbook of Pediatrics. 16th ed. Philadelphia: Saunders; 2000. p. 405. 6. Bickel H, Manz F.[] Additional laboratory findings include fasting hypoglycemia, ketonuria and hypercholesterolemia.[] Rev Endocr Metab Disord. 2003;4:95-102. Shin YS. Glycogen storage disease: Clinical, biochemical, and molecular heterogeneity. Semin Pediatr Neurol. 2006;13:115-20.[]

  • Kwashiorkor

    […] primer on the disorders and diseases that may affect the gastrointestinal tract in neonates and children.[] ケトン尿 ketonuria ケトン尿症 ketosis ケトーシス ketosis prone diabetes ketosis prone diabetes ketotic hypoglycemia ケトン性低血糖症 kidney biopsy 腎生検 kidney failure 腎不全 kidney transplantation[] References Krebs NF, Primak LE, Hambridge KM (2005) Normal childhood nutrition & its disorders. In: Hay. Current Pediatric Diagnosis & Treatment, 17th edn.[]

  • Heat Exhaustion

    Abstract This is a two-dimensional and Doppler echocardiographic study of the hemodynamic changes in patients with heatstroke and heat exhaustion. It demonstrates that the hemodynamic changes in severe heat exposure reflect a hyperdynamic circulation with tachycardia and high cardiac output states. Relative[…][]

  • Hypoglycemia

    Abstract CHARGE syndrome is a rare autosomal dominant disorder involving multiple organs.[] […] childhood or later with acute episodes of ataxia and vomiting Applies To Disturbances of metabolism of leucine, isoleucine, and valine Hypervalinemia Intermittent branched-chain ketonuria[] Pediatrics 1990;85:834-837. Cornblath M, Schwartz R. Disorders of Carbohydrate Metabolism in Infancy. 3rd ed. Philadelphia: W.B. Saunders, 1991, pp. 87-124, 225-246.[]

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