Literature DB >> 6696647

Neurological complications of hemoglobin SC disease.

R H Fabian, B H Peters.   

Abstract

The records of 68 patients with hemoglobin SC disease and 68 age- and sex-matched control patients were reviewed for neurological problems. A significant increase in retinopathy, stupor/coma, and seizures was noted in the hemoglobin SC group. Hemiplegia, noted in two young patients, was probably also secondary to hemoglobin SC disease. Hemoglobin SC disease may often go unrecognized as a cause of stupor and coma in older patients without other obvious manifestations of a sickling hemoglobinopathy. Factors known to precipitate sickling crisis and the associated neurological complications should be avoided, especially in patients undergoing surgery or parturition.

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Year:  1984        PMID: 6696647     DOI: 10.1001/archneur.1984.04050150067019

Source DB:  PubMed          Journal:  Arch Neurol        ISSN: 0003-9942


  1 in total

1.  Incidence of overt and covert neurological damage in children with sickle cell disease.

Authors:  P C Hindmarsh; M Brozovic; C G Brook; S C Davies
Journal:  Postgrad Med J       Date:  1987-09       Impact factor: 2.401

  1 in total

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