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94 Possible Causes for Splenomegaly, Steatorrhea, Vitamin D Deficiency

  • 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.[]

  • 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[]

  • Obstructive Jaundice

    USG abdomen showed a liver of normal size and echo pattern with intrahepatic biliary radicle dilatation (IHBRD) in the left lobe, splenomegaly (18 cm), normal common bile[] If left untreated, it will lead to malabsorption , particularly of vitamins A, D, E and K. The effects of these vitamin deficiencies will also be evident.[] After four weeks, a new abdominal computed tomography scan depicted dilated intrahepatic ducts, a soft mass surrounding the porta hepatis, splenomegaly and the same enlarged[]

  • 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.[]

  • Chronic Pancreatitis

    […] gradual tapering Pancreatic pseudocysts In approximately 50% of patients with chronic calcific pancreatitis, the pancreatic parenchyma contains cysts of varying sizes Ascites Splenomegaly[] Further considering the possible role of vitamin D deficiency in the pathogenesis of type 1 diabetes mellitus and the association of low vitamin D levels and poor glycemic[] Nausea and vomiting Steatorrhea: Frequent, oily, foul-smelling bowel movements.[]

  • Celiac Disease

    Herein, we report a case of a young female with CD in early phase in concordance with MC and splenomegaly.[] Osteopenia and osteoporosis might cause bone pain for several reasons, including defective calcium transport by the diseased small intestine, vitamin D deficiency, and binding[] , and nutritional and vitamin deficiencies Applies To Celiac: crisis infantilism rickets Gee (-Herter) disease Gluten enteropathy Idiopathic steatorrhea Nontropical sprue[]

  • Pancreatic Insufficiency - Anemia - Hyperostosis Syndrome

    Splenomegaly MedGen UID: 52469 • Concept ID: C0038002 • Finding Abnormal enlargement of the spleen.[] D 25-hydroxylation-deficient, type 1B CYP2R1 Rickets, vitamin D dependent, type 1 CYP27B1 Rickets, vitamin D-resistant, type 2A VDR Sarcoidosis, early-onset NOD2 Selective[] […] hyperostosis パスウェイ hsa00190 酸化的リン酸化 hsa01100 代謝パスウェイ 病因遺伝子 COX4I2 [HSA: 84701 ] [KO: K02263 ] コメント Shwachman-Bodian-Diamond, Pearson, and Johanson-Blizzard syndromes also show steatorrhea[]

  • Brandt Syndrome

    […] more ] 0003593 Irritability Irritable 0000737 Lethargy 0001254 Low alkaline phosphatase Decreased serum alkaline phosphatase 0003282 Recurrent candida infections 0005401 Splenomegaly[] deficiency Pseudovitamin D deficiency Vitamin D receptor defect E83.39 Other disorders of phosphorus metabolism Inclusion term(s): Acid phosphatase deficiency Hypophosphatasia[] 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[]

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