Literature DB >> 2733052

Hemoglobinopathies in a general and family practice setting.

C M Carr, K D Chapatwala, A K Nandedkar.   

Abstract

The incidence of sickle cell trait varies among blacks in North America. Although the average hemoglobin (Hb)-AS gene frequency is 8% in the United States, a value of 13.4% was recorded in South Carolina. Preliminary studies during a two-day community sponsored health fair in Selma, Alabama, revealed a sickle cell gene frequency of 15.96%. This study also found an intermediate frequency of 12.4% in a family practice center that is accredited for a residency program. Through a screening program, sickle cell trait was detected, a rigorous training program for resident physicians in family practice was implemented, and proper counseling to patients with hemoglobinopathies was provided. In the authors' judgment, laboratory screening for sickle cell trait is a first step toward genetic counseling and medical practice by family physicians and general practitioners.

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Year:  1989        PMID: 2733052      PMCID: PMC2625969     

Source DB:  PubMed          Journal:  J Natl Med Assoc        ISSN: 0027-9684            Impact factor:   1.798


  9 in total

1.  Rapid celluose acetate electrophoresis. II. Qualitative and quantitative hemoglobin fractionation.

Authors:  R C BARTLETT
Journal:  Clin Chem       Date:  1963-06       Impact factor: 8.327

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Authors:  A R ROBINSON; M ROBSON; A P HARRISON; W W ZUELZER
Journal:  J Lab Clin Med       Date:  1957-11

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Authors:  R G Schneider; T S Hosty; G Tomlin; R Atkins
Journal:  Clin Chem       Date:  1974       Impact factor: 8.327

4.  Sickle-cell anemia and other hemoglobinopathies. Procedures and strategy for screening employing spots of blood on filter paper as specimens.

Authors:  M D Garrick; P Dembure; R Guthrie
Journal:  N Engl J Med       Date:  1973-06-14       Impact factor: 91.245

Review 5.  Sickle cell anemia and related hemoglobinopathies.

Authors:  E P Vichinsky; B H Lubin
Journal:  Pediatr Clin North Am       Date:  1980-05       Impact factor: 3.278

6.  Direct identification of sickle cell anemia by blot hybridization.

Authors:  R F Geever; L B Wilson; F S Nallaseth; P F Milner; M Bittner; J T Wilson
Journal:  Proc Natl Acad Sci U S A       Date:  1981-08       Impact factor: 11.205

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Authors:  A L Gore
Journal:  Ala Med       Date:  1984-01

Review 8.  Methods for detection of hemoglobin variants and hemoglobinopathies in the routine clinical laboratory.

Authors:  R G Schneider
Journal:  CRC Crit Rev Clin Lab Sci       Date:  1978

9.  Sickle cell anemia in two White American children: essential laboratory criteria for diagnosis.

Authors:  P A Noronha; G R Honig
Journal:  Pediatrics       Date:  1979-02       Impact factor: 7.124

  9 in total

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