Title |
Sexuality and sickle cell anemia
|
---|---|
Published in |
Hematology Transfusion and Cell Therapy, January 2013
|
DOI | 10.5581/1516-8484.20130027 |
Pubmed ID | |
Authors |
Viviane de Almeida Côbo, Cibele Alves Chapadeiro, João Batista Ribeiro, Helio Moraes-Souza, Paulo Roberto Juliano Martins |
Abstract |
Sickle cell disease, the most common hereditary blood disease in the world, is the result of an atypical hemoglobin called S (Hb S) which, when homozygous (Hb SS) is the cause of sickle cell anemia. Changes of puberty, correlated with a delayed growth spurt, begin late in both male and female sickle cell anemia individuals with repercussions on sexuality and reproduction. The objectives of this exploratory and descriptive study were to characterize the development of sexuality in adults with sickle cell anemia by investigating the patient's perception of their sex life, as well as the information they had and needed on this subject. |
X Demographics
Geographical breakdown
Country | Count | As % |
---|---|---|
United States | 3 | 38% |
Antigua and Barbuda | 1 | 13% |
Nigeria | 1 | 13% |
Unknown | 3 | 38% |
Demographic breakdown
Type | Count | As % |
---|---|---|
Members of the public | 8 | 100% |
Mendeley readers
Geographical breakdown
Country | Count | As % |
---|---|---|
Unknown | 56 | 100% |
Demographic breakdown
Readers by professional status | Count | As % |
---|---|---|
Student > Doctoral Student | 9 | 16% |
Student > Bachelor | 9 | 16% |
Student > Master | 8 | 14% |
Student > Postgraduate | 6 | 11% |
Professor | 3 | 5% |
Other | 9 | 16% |
Unknown | 12 | 21% |
Readers by discipline | Count | As % |
---|---|---|
Medicine and Dentistry | 25 | 45% |
Biochemistry, Genetics and Molecular Biology | 6 | 11% |
Nursing and Health Professions | 5 | 9% |
Agricultural and Biological Sciences | 3 | 5% |
Psychology | 2 | 4% |
Other | 2 | 4% |
Unknown | 13 | 23% |