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205 Possible Causes for Splenomegaly, Steatorrhea, Vitamin D Deficiency

  • 3Beta-Hydroxy-Delta5-C27-Steroid Oxidoreductase Deficiency

    Clinical features include hepatomegaly with or without splenomegaly, jaundice, fat and fat-soluble vitamin malabsorption, and mild steatorrhea.[] Malabsorption leads to vitamin deficiency and can result is various symptoms including rickets, a condition marked by softened, weakened bones (vitamin D deficiency), vision[] Hepatomegaly, splenomegaly, and steatorrhea are also common symptoms that complete the clinical picture, alongside vitamin deficiencies.[]

  • Progressive Familial Intrahepatic Cholestasis

    […] cholesterol cholelithiasis • MDR3 disease PFIC3 presents during infancy with pruritus, jaundice, pale stools, hepatomegaly, or complications of portal hypertension, such as splenomegaly[] Biochemistry showed vitamin D deficiency and a skeletal survey revealed rickets and multiple pathological fractures.[] […] jaundice Dark urine Physical See the list below: Pruritus Scratching Cutaneous mutilation Irritability in infants Jaundice Scleral icterus Cutaneous jaundice Hepatomegaly Splenomegaly[]

  • Congenital Bile Acid Synthesis Defect Type 2

    The latter comprise nyctalopia and xerophthalmia due to vitamin A deficiency, bone pain and and skeletal deformities because of vitamin D deficiency, and a propensity to bleed[] The clinical presentation resembles that of congenital BAS defect type 1 (see this term) with hepatosplenomegaly, jaundice, fat-soluble vitamin malabsorption, and steatorrhea[] Because bile acids are required for the absorption of fat-soluble vitamins, namely vitamins A, D, E, and K, affected infants may also present symptoms of vitamin deficiency[]

  • Hemochromatosis

    Regression on SF revealed significant associations: TS; male sex; age; GGT; transfusion units (positive); and splenomegaly (negative) (p 0.0001, 0.0016, 0.0281, 0.0025, 0.0001[] ( E58 - E61 ) parathyroid disorders ( E20 - E21 ) vitamin D deficiency ( E55.- ) Disorders of mineral metabolism E83.1 ICD-10-CM Diagnosis Code E83.1 Disorders of iron metabolism[] Here we report the case of a 16-year-old Chinese boy, who was admitted with hepatalgia, jaundice, hyperpigmentation, and splenomegaly to our hospital.[]

  • Inflammatory Bowel Disease

    […] deficiency (PD) is an inherited disorder associated with cutaneous ulcers, intellectual disability, unusual facial appearance, skeletal deformities, hematological anomalies, splenomegaly[] This review aims to summarise the latest knowledge on the extraskeletal effects of vitamin D in IBD, and outlines the potential deleterious consequences of vitamin D deficiency[] "Association Between Inflammatory Bowel Disease and Vitamin D Deficiency: A Systematic Review and Meta-analysis" .[]

  • Primary Biliary Cirrhosis

    […] of the caudate lobe hepatic surface irregularity due to regenerative nodules regional lymphadenopathy: tends to dominate in the gastrohepatic ligament and porta hepatis 4 splenomegaly[] Fanconi syndrome with renal tubular acidosis, vitamin D deficiency and primary biliary cirrhosis were related to the pathogenesis of osteomalacia in this case.[] In June 2008, she was admitted with intrahepatic cholestasis, steatorrhea, and spontaneous fractures of various ribs.[]

  • Brandt Syndrome

    […] more ] 0003593 Irritability Irritable 0000737 Lethargy 0001254 Low alkaline phosphatase Decreased serum alkaline phosphatase 0003282 Recurrent candida infections 0005401 Splenomegaly[] ( E58 - E61 ) parathyroid disorders ( E20 - E21 ) vitamin D deficiency ( E55.- ) Disorders of mineral metabolism Approximate Synonyms Disorder of zinc metabolism Zinc metabolism[] Diarrhea and steatorrhea are possible causes for the development of acquired acrodermatitis enteropathica. [1,3] History of renal diseases [1] History of renal tubular disease[]

  • Intestinal Lymphangiectasia

    On physical examination he was shown to have, limbs oedemas, ascites, and splenomegaly.[] Complicated vitamin D deficiency [low serum 25-hydroxy vitamin D concentration ( 12.48 mmol/L, the detection limit)] and secondary hyperparathyroidism were confirmed via blood[] Chronic diarrhea and steatorrhea occur frequently in patients with autoimmune polyglandular syndrome (APS) type I.[]

  • Calcific Pancreatitis

    On examination, macroglossia and periorbital purpura (Fig 1) were present with mild splenomegaly.[] Vitamin D deficiency is prevalent in chronic pancreatitis (CP), but the optimal route and dose of vitamin D supplementation are unknown.[] Four years later, she presented with steatorrhea with osteomalacia and secondary hyperparathyroidism, a rare occurrence in chronic pancreatitis.[]

  • Hyperlipoproteinemia Type 5

    This thoroughly updated edition includes new information on metabolic syndrome, immuno-nutrition, and vitamin D deficiency.[] VLDL, & Chylomicrons Low Cholesterol & TG Burr cells (acanthocytes) A-beta-lipoproteinemia Bassen-Kornzweig Syndrome Burr cells (acanthocytes) Failure to thrive Diarrhea, steatorrhea[] Affected children have slow growth and weight gain, frequent (chronic) diarrhea, and foul-smelling stools (steatorrhea).[]

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