Literature DB >> 7091575

Problems and complications in the adolescent with sickle cell disease.

D L Wethers.   

Abstract

The period of adolescence in the patient with sickle cell disease seems to be a period of relative calm, medically speaking. The current 5-year prospective Cooperative Study of the Clinical Course of Sickle Cell Disease should demonstrate the actual spectrum of disease in this age group. The recent literature documents with significant relationship between retardation of growth and sexual maturation in the child with sickle cell disease, an effect which seems independent of the severity of the disease. Several other major problems in the adolescent are discussed, including psychological disturbances, leg ulcers, aseptic necrosis, pulmonary disease, priapism, stroke, cholelithiasis, and birth control. A retrospective series of 76 cases of sickle cell disease is briefly presented and the complication occurring during the second decade of life are reviewed.

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Year:  1982        PMID: 7091575

Source DB:  PubMed          Journal:  Am J Pediatr Hematol Oncol        ISSN: 0192-8562


  4 in total

1.  Health-related stigma in young adults with sickle cell disease.

Authors:  Coretta M Jenerette; Cheryl Brewer
Journal:  J Natl Med Assoc       Date:  2010-11       Impact factor: 1.798

2.  Perceived barriers to clinic appointments for adolescents with sickle cell disease.

Authors:  Lori E Crosby; Avani C Modi; Kathleen L Lemanek; Shanna M Guilfoyle; Karen A Kalinyak; Monica J Mitchell
Journal:  J Pediatr Hematol Oncol       Date:  2009-08       Impact factor: 1.289

3.  The effectiveness of biofeedback-assisted relaxation in modifying sickle cell crises.

Authors:  L Cozzi; W W Tryon; K Sedlacek
Journal:  Biofeedback Self Regul       Date:  1987-03

4.  Multiple complications in a sickle cell disease patient: a case report.

Authors:  J A Olaniyi
Journal:  Clin Med Case Rep       Date:  2008-07-08
  4 in total

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