hemoglobin S/beta thalassemia 0
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Pathology
- vasoocclusive crises
- aseptic necrosis of bone
Clinical manifestations
- episodic abdominal pain (case report)
- gallstones[3] (case report)
Laboratory
- complete blood count (CBC)
- microcytic anemia
- blood hemoglobin 7-9 g/dL[2]
- MCV 60-80 fL
- microcytic anemia
- peripheral smear
- hemoglobin electrophoresis:
- serum unconjugated bilirubin elevated
Radiology
- abdominal CT (images)[3]
More general terms
References
- ↑ Harrison's Principles of Internal Medicine, 14th ed. Fauci et al (eds), McGraw-Hill Inc. NY, 1998, pg 648
- ↑ 2.0 2.1 Medical Knowledge Self Assessment Program (MKSAP) 17, American College of Physicians, Philadelphia 2015
- ↑ 3.0 3.1 3.2 Gupta A, Jain P Calcified Spleen and Gallstones N Engl J Med 2018; 378:380. Jan 25, 2018 <PubMed> PMID: https://www.ncbi.nlm.nih.gov/pubmed/29365300 Free full text <Internet> http://www.nejm.org/doi/full/10.1056/NEJMicm1703915
- ↑ Benites BD, Bastos SO, Baldanzi G et al Sickle cell/beta-thalassemia: Comparison of Sbeta0 and Sbeta+ Brazilian patients followed at a single institution. Hematology. 2016 Dec;21(10):623-629. Epub 2016 May 28. PMID: https://www.ncbi.nlm.nih.gov/pubmed/27237196