Literature DB >> 6396021

Osteoarticular manifestations in sickle-cell disorders.

P Kaklamanis.   

Abstract

The osteoarticular manifestations of the main sickling disorders (homozygous sickle cell-HbSS anaemia-, double heterozygous-HbS-beta thalassaemia, double heterozygous HbS-C disease and sickle cell-trait) are reviewed; They may be grouped into 3 main categories: vaso-occlusive, infective and metabolic. The pathophysiology and pathogenesis as well as the treatment are discussed.

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Year:  1984        PMID： 6396021     DOI： 10.1007/BF02031264

Source DB:  PubMed          Journal:  Clin Rheumatol        ISSN： 0770-3198            Impact factor:   2.980


  82 in total

1.  The bone changes in sickle cell anaemia and its genetic variants.

Authors:  J S GOLDING; J E MACIVER; L N WENT
Journal:  J Bone Joint Surg Br       Date:  1959-11

2.  Gout and blood dyscrasias.

Authors:  J H TALBOTT
Journal:  Medicine (Baltimore)       Date:  1959-05       Impact factor: 1.889

3.  Aseptic necrosis of bone in Caucasians with chronic hemolytic anaemia due to combined sickling and thalassemia traits.

Authors:  R S REICH; N J ROSENBERG
Journal:  J Bone Joint Surg Am       Date:  1953-10       Impact factor: 5.284

4.  Aseptic necrosis of the femoral heads in sickle-A hemoglobin disease.

Authors:  S Blau; D Hamerman
Journal:  Arthritis Rheum       Date:  1967-08

5.  Serratia osteomyelitis in sickle cell disease.

Authors:  J Fonk; J D Coonrod
Journal:  JAMA       Date:  1971-07-05       Impact factor: 56.272

6.  Hemarthrosis and sickle cell trait.

Authors:  D F Casey; E S Cathcart
Journal:  Arthritis Rheum       Date:  1970 Nov-Dec

Review 7.  Clinical diversity of sickle cell anemia: genetic and cellular modulation of disease severity.

Authors:  M H Steinberg; R P Hebbel
Journal:  Am J Hematol       Date:  1983-06       Impact factor: 10.047

8.  Sternal cupping: a new finding in childhood sickle cell anemia.

Authors:  M S Levine; S Borden; F M Gill
Journal:  Radiology       Date:  1982-02       Impact factor: 11.105

9.  Natural history of sickle cell anemia in Saudi Arabs. A study of 270 subjects.

Authors:  R P Perrine; M E Pembrey; P John; S Perrine; F Shoup
Journal:  Ann Intern Med       Date:  1978-01       Impact factor: 25.391

10.  Sickle cell disease associated with uric acid deposition disease.

Authors:  B M Rothschild; C W Sienknecht; S B Kaplan; J S Spindler
Journal:  Ann Rheum Dis       Date:  1980-08       Impact factor: 19.103
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