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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.[malacards.org] Malabsorption leads to vitamin deficiency and can result is various symptoms including rickets, a condition marked by softened, weakened bones (vitamin D deficiency), vision[rarediseases.org] Hepatomegaly, splenomegaly, and steatorrhea are also common symptoms that complete the clinical picture, alongside vitamin deficiencies.[symptoma.com]

  • 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[basicmedicalkey.com] Biochemistry showed vitamin D deficiency and a skeletal survey revealed rickets and multiple pathological fractures.[ncbi.nlm.nih.gov] […] jaundice Dark urine Physical See the list below: Pruritus Scratching Cutaneous mutilation Irritability in infants Jaundice Scleral icterus Cutaneous jaundice Hepatomegaly Splenomegaly[emedicine.medscape.com]

  • 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[symptoma.com] The clinical presentation resembles that of congenital BAS defect type 1 (see this term) with hepatosplenomegaly, jaundice, fat-soluble vitamin malabsorption, and steatorrhea[orpha.net] 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[symptoma.com]

  • 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[ncbi.nlm.nih.gov] ( 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[icd10data.com] Here we report the case of a 16-year-old Chinese boy, who was admitted with hepatalgia, jaundice, hyperpigmentation, and splenomegaly to our hospital.[ncbi.nlm.nih.gov]

  • Inflammatory Bowel Disease

    […] deficiency (PD) is an inherited disorder associated with cutaneous ulcers, intellectual disability, unusual facial appearance, skeletal deformities, hematological anomalies, splenomegaly[ncbi.nlm.nih.gov] 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[ncbi.nlm.nih.gov] "Association Between Inflammatory Bowel Disease and Vitamin D Deficiency: A Systematic Review and Meta-analysis" .[en.wikipedia.org]

  • 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[radiopaedia.org] Fanconi syndrome with renal tubular acidosis, vitamin D deficiency and primary biliary cirrhosis were related to the pathogenesis of osteomalacia in this case.[ncbi.nlm.nih.gov] In June 2008, she was admitted with intrahepatic cholestasis, steatorrhea, and spontaneous fractures of various ribs.[ncbi.nlm.nih.gov]

  • Brandt Syndrome

    […] more ] 0003593 Irritability Irritable 0000737 Lethargy 0001254 Low alkaline phosphatase Decreased serum alkaline phosphatase 0003282 Recurrent candida infections 0005401 Splenomegaly[rarediseases.info.nih.gov] ( E58 - E61 ) parathyroid disorders ( E20 - E21 ) vitamin D deficiency ( E55.- ) Disorders of mineral metabolism Approximate Synonyms Disorder of zinc metabolism Zinc metabolism[icd10data.com] 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[explainmedicine.com]

  • Intestinal Lymphangiectasia

    On physical examination he was shown to have, limbs oedemas, ascites, and splenomegaly.[elsevier.es] 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[ncbi.nlm.nih.gov] Chronic diarrhea and steatorrhea occur frequently in patients with autoimmune polyglandular syndrome (APS) type I.[ncbi.nlm.nih.gov]

  • Calcific Pancreatitis

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

  • Hyperlipoproteinemia Type 5

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

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