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1,294 Possible Causes for Phenylketonuria, Vomiting

  • Poisoning

    The first is phenylketonuria (PKU). One out of 20,000 babies is born without the ability to metabolize phenylalanine, one of the two amino acids in aspartame.[] The symptoms of vomiting, abdominal pain, diarrhea, hematochezia, and hematuria disappeared gradually.[] Staphylococcus aureus Nausea, vomiting, stomach cramps and diarrhoea.[]

  • Ileus

    Postoperative nausea and vomiting have high incidences.[] A 7-y-old girl with phenylketonuria and long-term constipation was admitted to the emergency department with symptoms of seizure, vomiting and abdominal distention.[] Vomiting was present in two patients from group A and in eight from group B (6.25 vs. 25.0%; p 0.03).[]

  • Morphine

    Nausea and vomiting are probably the most unpleasant side effects that occur when morphine used.[] Caution is advised if you have diabetes , alcohol dependence , liver disease, phenylketonuria (PKU), or any other condition that requires you to limit/avoid these substances[] Thirty minutes after admission to the post-anesthesia recovery unit the patient developed vomiting and diaphoresis being treated with 0.4 mg of naloxone followed by continuous[]

  • Hereditary Fructose Intolerance

    This is a report of a five-year-old girl with phenylketonuria (PKU) and hereditary fructose intolerance (HFI) who underwent elective strabismus surgery.[] Feeding difficulties (20X), vomiting (18X), and failure to thrive (16X) were leading symptoms.[] Classical phenylketonuria (PKU) and hereditary fructose intolerance (HFI) are two inborn errors of metabolism that have an autosomal recessive mode of inheritance.[]

  • Citrullinemia

    This article incorporates public domain text from this source) References v t e Metabolic pathology / Inborn error of metabolism ( E70-90 , 270-279 ) Amino acid Aromatic ( Phenylketonuria[] All three had episodes of vomiting, lethargy and hyperammonemia shortly after birth. The two more severe cases developed convulsions.[] We report the case of a 56-year-old woman with a history of episodes of vomiting and coma.[]

  • Urea Cycle Disorder

    Xp21.1)* Biochemical profile: Elevated ornithine and glutamine, decreased citrulline and arginine , markedly increased urine orotate Clinical features: In males, recurrent vomiting[] The most well known disorder in the larger group is phenylketonuria (PKU), characterized by an accumulation of the amino acid phenylalanine, which frequently results in mental[] Phenylketonuria Scientific Review Conference: State of the science and future research needs. Mol Genet Metab. 2014;112(2):87-122. Chin HL, Aw MM, Quak SH, et al.[]

  • Hydatidiform Mole

    The pregnancy was unremarkable except for the complaints of excessive nausea and vomiting.[] Strict control of hyperphenylalaninemia is necessary in pregnant women with phenylketonuria (PKU) in order to prevent phenylalanine embryopathy in the fetus, characterized[] The patient was admitted to our clinic complaining of acute abdominal pain, nausea and vomiting lasting one day.[]

  • Methylmalonic Acidemia

    She had clinical signs of diabetic ketoacidosis such as dehydration, deep sighing respiration, smell of ketones, lethargy, and vomiting.[] All 50 states screen newborns for phenylketonuria (PKU). Most states also test newborns for galactosemia.[] The clinical signs are recurrent episodes of ketoacidosis and bouts of vomiting, dehydration and mental retardation.[]

  • Hypervitaminosis A

    […] syndrome E67.3 Hypervitaminosis D E67.8 Other specified hyperalimentation E68 Sequelae of hyperalimentation E70 Disorders of aromatic amino-acid metabolism E70.0 Classical phenylketonuria[] Acutely, patients may present with non-specific manifestations that include nausea, vomiting, and anorexia.[] Symptoms of acute Vitamin A toxicity include: Drowsiness Abdominal Pain Nausea Vomiting Symptoms of chronic Vitamin A toxicity include: Blurry vision Swelling of the bones[]

  • Galactosemia

    Therefore, we performed a cross-sectional study in parents of children with phenylketonuria (PKU, OMIM #261600) and galactosemia (OMIM #230400), metabolic disorders not affecting[] The presenting symptoms which include vomiting, diarrhea, jaundice, and failure to thrive result from the ingestion of foods containing galactose--breast milk and formulas[] […] occupational outcome as well as health-related quality of life (HRQOL) in adult German patients with galactosemia and to compare information with data from patients with phenylketonuria[]

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