Literature DB >> 8121868

Haemoglobin-H disease presenting with microcytic hypochromic anaemia in an 81 year old woman.

O M Jolobe1.   

Abstract

Over an 11 year period, the diagnosis of haemoglobin-H (Hb-H) disease was missed in a Caucasian woman of British stock who first presented with microcytic hypochromic anaemia at the age of 81. The diagnosis was confirmed at the age of 92, when the typical inclusions of Hb-H disease were demonstrated in erythrocytes stained with brilliant cresyl blue, and the presence of Hb-H was documented by haemoglobin electrophoresis. She subsequently developed biliary obstruction due either to an inflammatory polyp associated with choledocholithiasis or ampullary carcinoma.

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Year:  1993        PMID: 8121868      PMCID: PMC2400013          DOI: 10.1136/pgmj.69.818.930

Source DB:  PubMed          Journal:  Postgrad Med J        ISSN: 0032-5473            Impact factor:   2.401


  5 in total

1.  HAEMOGLOBIN H DISEASE IN AN ENGLISH FAMILY.

Authors:  J C WOODROW; R L NOBLE; J H MARTINDALE
Journal:  Br Med J       Date:  1964-01-04

2.  Hemoglobin H; clinical, laboratory, and genetic studies of a family with a previously undescribed hemoglobin.

Authors:  D A RIGAS; R D KOLER; E E OSGOOD
Journal:  J Lab Clin Med       Date:  1956-01

3.  Concurrence of hereditary spherocytosis and alpha thalassaemia.

Authors:  D C Heaton; A P Fellowes; P M George
Journal:  Aust N Z J Med       Date:  1991-08

4.  -thalassemia in the American Negro.

Authors:  E Schwartz; J Atwater
Journal:  J Clin Invest       Date:  1972-02       Impact factor: 14.808

5.  Extrahepatic biliary obstruction by a common bile duct inflammatory polyp in association with a gallstone, and treatment by endoscopic sphincterotomy.

Authors:  H A Shepherd; J M Laidlow; A P Ross; A Vincenti; R H Lane
Journal:  Endoscopy       Date:  1986-03       Impact factor: 10.093

  5 in total

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