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16 Possible Causes for Intermittent Jaundice, Pediatric Disorder, Uric Acid Increased

  • Hereditary Spherocytosis

    The 2003 Healthcare Cost and Utilization Project (HCUP) Kids’ Inpatient Database (KID), a robust and widely used measure of pediatric disorders, has estimated that the number[] Abstract Hereditary spherocytosis is an autosomal dominant congenital hemolytic anemia due to defect in RBC membrane protein that commonly presents with intermittent jaundice[] . * Department of Pediatrics, University of Texas Southwestern Medical Center † Center for Cancer and Blood Disorders, Children’s Medical Center, Dallas, TX ‡ Department of[]

  • Hepatorenal Syndrome

    Farahnak Assadi, Fluid and Electrolyte Disorders, Clinical Decisions in Pediatric Nephrology, 10.1007/978-0-387-74602-9_1, (1-68), (2008).[] Wui-Chiang Lee, Han-Chieh Lin, Ming-Chih Hou, Hsiao-Yi Lin, Fa-Yauh Lee, Sun-Sang Wang, Full-Young Chang and Shou-Dong Lee , Serum Uric Acid Levels in Patients With Cirrhosis[] Severe circulatory dysfunction (mean arterial pressure usually is 70 mm Hg) and very low systemic vascular resistance. • Severe liver disease, with jaundice, coagulopathy,[]

  • Congenital Liver Cirrhosis

    Contact the Pediatric Surgery Service at: 617-726-0270 Pediatric Liver and Biliary Disease Center Pediatric Patients Only The Pediatric Liver and Biliary Disease Center at[] acid level elevated Maternal mortality, 1%; prematurity and fetal death, 5%-30% Beta blocker, methyldopa, magnesium sulfate; early delivery HELLP syndrome Beyond 22 wk and[] He had intermittent high grade fever with dry cough and respiratory distress for 4 days duration.[]

  • Hexokinase Deficiency

    […] hematologic disorders, including newly recognized ones.[] Uric Acid), and the patient presents Hyperuricemia.[] Intermittent jaundice and premature pigment gallstones are common. Splenomegaly is characteristic (palpable in 75% to 80% of cases).[]

  • Tyrosinemia

    Topics: Inborn Errors Of Metabolism Metabolic Disorders Pediatrics[] The tubular handling of phosphorus, uric acid, beta 2-microglobulin, and amino acids was disturbed. Low urinary osmolality was also seen.[] The acute onset may be dramatic, with hepatomegaly, jaundice, epistaxis, melaena, purpuric lesions, marked oedema, and the distinctive cabbage-like odour.[]

  • Hypercholesterolemia

    Gout or increased uric acid.[] RESULT AND CONCLUSION: In addition, specific disorders of cholesterol metabolism, such as Familial Hypercholesterolemia (FH) may be encountered in a pediatric practice.[] We report the case of a male infant who had developed failure to thrive, jaundice, intermittent pruritus, and multiple diffuse symmetrical skin xanthomas at 1 year of age.[]

  • Primary Biliary Cirrhosis

    […] patients with Alagille syndrome (ALGS), a rare, life-threatening genetic disorder that presents with chronic cholestasis (accumulation of bile acids in the liver) and severe[] Twenty four hour urine demonstrated a low renal fractional tubular reabsorption of phosphate, increased fractional excretion of uric acid and generalized aminoaciduria.[] Reddy AN, Grosberg SJ, Wapnick S: Intermittent cholestatic jaundice and nonmetastatic prostatic carcinoma. Arch Intern Med 1977;137:1616–1618.[]

  • Refractory Megaloblastic Anemia

    J Pediatr 2009;155:888-92. [ PUBMED ] [ FULLTEXT ] 4. Naeem MA, Shabaz A, Shoaib A, Usman M.[] […] degree of in effective erythropoiesis · Haptoglobins, Uric acid and alkaline phosphatase levels – Decreased. · Serum methylmalonate and homocystein levels - Vitamin B-12[] He has a fever and you note jaundice. You order an ultrasound of his abdomen and find multiple gallstones. Lab results: Hct .36 L/L; Hgb 120 g/L. PBS at right.[]

  • Progressive Retinal Dystrophy due to Retinol Transport Defect

    This book is a 'must have' for pediatric ophthalmologists, retina specialists, and geneticists.[] […] serum uric acid levels. ( 27151312 ) Solak B....Solak Y. 2016 15 Relationship between acne vulgaris and attention-deficit/hyperactivity disorder symptoms in a clinical sample[] […] sinusitis Abnormality of the cerebral vasculature Thyroiditis Vitamin E deficiency Antinuclear antibody positivity Abnormality of the thyroid gland Prostatitis Macular atrophy Intermittent[]

  • Glucose-6-Phosphate Dehydrogenase Deficiency

    OBJECTIVE: Glucose-6-phosphate dehydrogenase (G6PD) deficiency is a major contributor to neonatal hyperbilirubinemia, yet newborn screening for this disorder in the United[] An acid urine pH favors production of poorly soluble uric acid over the more soluble urate, increasing the risk for precipitation of intratubular uric acid crystals.[] To determine whether you have an inherited G6PD deficiency When a child experienced persistent jaundice as a newborn for unknown reasons; when you have had one or more intermittent[]

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