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11 Possible Causes for Cholelithiasis, Hyperuricemia, Physiological Neonatal Jaundice

  • Obesity

    […] tolerance, acanthosis nigricans, hepatic steatosis, premature puberty, hypogonadism and polycystic ovary syndrome, obstructive sleep disorder, orthopedic complications, cholelithiasis[ncbi.nlm.nih.gov] Shadick NAKim RWeiss SLiang MHSparrow DHu H Effect of low level lead exposure on hyperuricemia and gout among middle aged and elderly men: the Normative Aging Study.[doi.org] […] effects of infection and, in one case, neonatal death.[doi.org]

  • Hereditary Spherocytosis

    This is a report of an 11 years old male diagnosed case of hereditary spherocytosis who presented with jaundice, splenomegaly and cholelithiasis.[ncbi.nlm.nih.gov] Applicable To Neonatal physiological jaundice (intense)(prolonged) NOS spherocytosis D58.0 (congenital) Spherocytosis (congenital) (familial) (hereditary) D58.0 hemoglobin[icd10data.com] In this paper we describe how we perform laparoscopic splenectomy plus cholecystectomy at the same time to treat hereditary spherocytosis combined with cholelithiasis in two[ncbi.nlm.nih.gov]

  • Rotor Syndrome

    […] hemolytic jaundice, prehepatic jaundice, hepatic jaundice, posthepatic jaundice, obstructive jaundice, wilson's disease, hepatitis virus B, hepatitis virus C, HBV, HCV, Cholelithiasis[slideshare.net] Respiratory ) - Mixed disorder of acid-base balance - H 2 O Dehydration / Hypervolemia - K Hypokalemia / Hyperkalemia - Cl Hyperchloremia / Hypochloremia Purine and pyrimidine Hyperuricemia[wikidoc.org] Neonatal jaundice and Breast-milk jaundice Conjugated hyperbilirubinaemia Hepatocellular – Diminished hepatocyte function.[lifeinthefastlane.com]

  • Pneumatosis Vaginalis

    Children with hemoglobinopathies or hemolytic diseases are at great risk for cholelithiasis.[elearning.sumdu.edu.ua] LESCH-NYHAN SYNDROME: Deficiency of HGPRT (Hypoxanthine-Guanine Phospho-ribosyltransferase ------ Hyperuricemia, uric acid kidney stones Choreoathetosis Mental retardation[aippg.net] Crigler-Najjar syndrome B. jaundice due to parenteral nutrition C. neonatal hepatitis D. physiologic jaundice E. pyloric stenosis 27- Early hospital discharge is defined as[prep4usmle.com]

  • Cervical Spina Bifida with Hydrocephalus

    白血病肝浸潤:leukemic cell infiltration 2)胆道 先天性胆道閉鎖症:congenital biliary atresia 先天性総胆管拡張症:congenital choledochal cyst 胆嚢コレステリン沈着症:cholesterolosis コレステリンポリープ:cholesterin polyp 胆石症:cholelithiasis[medical-e.net] […] deficiency, adult onset Glycogen storage disease due to acid maltase deficiency, infantile onset Glycogen storage disease due to acid maltase deficiency, juvenile onset Hyperuricemia-pulmonary[csbg.cnb.csic.es] […] day when jaundice appears (physiologic jaundice).[quizlet.com]

  • Marfanoid Habitus with Situs Inversus

    […] atypical T cells Sezary syndrome (cutaneous T cell lymphoma)/ mycosis fungoides Facial muscle spasm upon tapping Chvostek's sign (hypocalcemia) Fat, female, forty, and female Cholelithiasis[studyblue.com] […] accumulation of adenosine is toxic to lymphocytes) -X-linked Recessive -Absence of HGPRT -- defective purine salvage -Findings: retardation, self-mutilation, aggression, hyperuricemia[brainscape.com] Jaundice Physiologic jaundice of the newborn resolves by 1-2 weeks Tx: frequent feeds, natural sunlight/phototherapy if t bili 20-25-- exchange transfusion Biliary atresia[flashcardbook.com]

  • Hardikar Syndrome

    A Greek study of 198 adult patients with cholelithiasis, along with 152 controls, also found evidence of an association between Gilbert syndrome and the development of cholelithiasis[emedicine.medscape.com] […] electroclinical syndrome Infantile Cataract, Skin Abnormalities, Glutamate Excess, and Impaired Intellectual Development infantile cerebellar-retinal degeneration Infantile Hyperuricemia[rgd.mcw.edu] Neonatal Jaundice and Ineffective Erythropoiesis Physiologic jaundice In physiologic jaundice, the peak total serum bilirubin level is 5-6 mg/dL (86-103 µmol/L), occurs at[emedicine.medscape.com]

  • Enteropathy, Familial with Villous Edema and IgG2 Deficiency

    Return to top THE GALLBLADDER CHOLELITHIASIS : Gallstones CHOLESTEROL GALLSTONES: Due to hypercholesterolemia.[kumc.edu] Gout Chemotherapy ------ higher DNA cell turnover rate ------ hyperuricemia Leukemia and polycythemia similarly lead to hyperuricemia due to increased cell turnover rate.[kumc.edu] This is a complication of physiologic jaundice, or can occur with Neonatal Hepatitis. CHOLESTASIS : Impeded flow of bile.[kumc.edu]

  • NISCH Syndrome

    Administration of ursodeoxycholic acid (UDCA) decreases bile stasis and prevents the formation of intrahepatic cholelithiasis.[frontiersin.org] […] dental morphology Nephrocalcinosis Nephropathy Proximal tubulopathy Gastrointestinal hemorrhage Meningitis Nausea Decreased liver function Hypophosphatemia Shock Glycosuria Hyperuricemia[mendelian.co] Introduction Neonatal physiological jaundice is a common and mostly benign symptom. It typically resolves 2 weeks after birth.[frontiersin.org]

  • Congenital Deficiency in Alpha-fetoprotein

    These include biliary atresia, choledochal cyst, biliary sludge or cholelithiasis, congenital hepatic fibrosis, inspissated bile syndrome, perforation of the bile duct, an[cancertherapyadvisor.com] Gout Chemotherapy ------ higher DNA cell turnover rate ------ hyperuricemia Leukemia and polycythemia similarly lead to hyperuricemia due to increased cell turnover rate.[kumc.edu] This is a complication of physiologic jaundice, or can occur with Neonatal Hepatitis. CHOLESTASIS : Impeded flow of bile.[kumc.edu]

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