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607 Possible Causes for Hereditary Spherocytosis

  • Cholelithiasis

    Hereditary spherocytosis, sickle cell anaemia and thalassemia are the haemolytic disorders most commonly associated with development of gall stones in paediatric age group[ncbi.nlm.nih.gov] Abstract The incidence of gall stones in thalassaemia is less than that in sickle cell anaemia or hereditary spherocytosis.[ncbi.nlm.nih.gov] Risk factors for pigment stones include hemolytic anemias (such as sickle-cell disease and hereditary spherocytosis), cirrhosis, and biliary tract infections.[hamrodoctor.com]

  • Cardiomyopathy

    Brain Dev. 2018 Jun;40(6):484-488. doi: 10.1016/j.braindev.2018.02.004. Epub 2018 Mar 2. Nishioka M 1 , Inaba Y 2 , Motobayashi M 3 , Hara Y 1 , Numata R 4 , Amano Y 4 , Shingu K 5 , Yamamoto Y 6 , Murayama K 7 , Ohtake A 8 , Nakazawa Y 1 . Author information 1 Department of Pediatrics, Shinshu University School of[…][ncbi.nlm.nih.gov]

  • Hereditary Spherocytosis

    Hereditary spherocytosis is a condition that affects red blood cells.[ghr.nlm.nih.gov] These changes are also seen in non-hereditary spherocytosis, but they are typically more pronounced in hereditary spherocytosis.[en.wikipedia.org] Hereditary spherocytosis is a common inherited disorder that is characterised by anaemia, jaundice, and splenomegaly.[ncbi.nlm.nih.gov]

  • Autoimmune Hemolytic Anemia

    spherocytosis, presence of numerous target cells and occasional HbC crystals on Pappenheim stained blood films.[doi.org] spherocytosis) Urinalysis hemoglobinuria hemosiderinuria Differential Diagnosis Treatment Warm agglutinin from best initial therapy to further steps in treatment ladder glucocorticoids[step1.medbullets.com] […] tests seemed compatible with an HbSC disease, showing typical laboratory features, namely a signifi-cant proportion of hyperchromic RBC, corresponding to secondary, non hereditary[doi.org]

  • Megaloblastic Anemia

    Spherocytosis: A Patient's Journey back to top Where Can I Find More Information?[hematology.org] As part of the family history, physicians should ask about the presence of certain hematologic syndromes, including sickle cell disease, hereditary spherocytosis, and glucose[aafp.org] […] also help prevent nutritional anemias; however, older adults should not take iron supplementsfor iron-deficiencyanemia unless instructed by their physicians. back to top Hereditary[hematology.org]

  • Acquired Hemolytic Anemia

    ) 15 HEREDITARY SPHEROCYTOSIS SPHEROCYTES – IN PERIPHERAL BLOOD SMEAR SPHEROCYTES UNABLE TO PASS THROUGH THE SPLEEN SEVERE CASES REQUIRE A SPLENECTOMY 16 HEREDITARY SPHEROCYTOSIS[slideplayer.com] spherocytosis, nonspherocytic congenital hemolytic anemia due to glucose-6-phosphate dehydrogenase deficiency, acquired hemolytic anemia and vitamin B12 deficiency induced[ncbi.nlm.nih.gov] Hereditary Spherocytosis (HS) Determine whether a patient may have hereditary spherocytosis (HS), given the history, physical examination, hemogram, peripheral blood smear[hematology.org]

  • Erythrocyte Membrane Abnormality

    […] blood* Elliptocytosis, Hereditary/complications Elliptocytosis, Hereditary/surgery Erythrocyte Membrane/metabolism* Erythrocytes Humans Spherocytosis, Hereditary/blood* Spherocytosis[ncbi.nlm.nih.gov] .: A red cell membrane protein abnormality in hereditary spherocytosis. Brit. J. Haemat. 23 , 363 (1972) PubMed Google Scholar 7.[link.springer.com] Notable among these are hereditary elliptocytosis (HE), hereditary spherocytosis (HS) and hereditary pyropoikilocytosis (HPP).[annsaudimed.net]

  • Congenital Hemolytic Anemia

    Basically classified by causative mechanism, types of congenital hemolytic anemia include: Genetic conditions of RBC Membrane Hereditary spherocytosis Hereditary elliptocytosis[en.wikipedia.org] Spherocytosis Abnormally small and lack central pallor Test used to diagnose Hereditary Spherocytosis Spherocytes are sequestered in this organ in Hereditary Spherocytosis[brainscape.com] Although the condition was transmitted as a dominant trait, it was not identified to the common hereditary spherocytosis.[ncbi.nlm.nih.gov]

  • Glossitis

    Abstract Herpes simplex virus (HSV) type 1 (HSV-1) infection of the tongue commonly accompanies acute primary herpetic gingivostomatitis. However, recurrent infection of the tongue is exceptional and is restricted to immunocompromised individuals. A 57-year-old man with corticosteroid-dependent chronic obstructive[…][ncbi.nlm.nih.gov]

  • Hereditary Elliptocytosis

    Abstract Hereditary elliptocytosis (HE), its aggravated form hereditary pyropoikilocytosis (HPP), and hereditary spherocytosis (HS) designate a set of congenital hemolytic[ncbi.nlm.nih.gov] Numerous mutations have allowed to reclassify hereditary elliptocytosis (HE) and poikilocytosis (HP), and, more recently, hereditary spherocytosis (HS) into well defined subsets[ncbi.nlm.nih.gov] Hereditary spherocytosis is characterized by hemolysis of spheroidal RBCs and anemia.[msdmanuals.com]

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