Endocrinologic Diseases in Hemoglobinopathies

被引：0
作者：
El Baba, Khaled
Zantout, Mira S. [1 ]
Azar, Sami T. [1 ]
机构：
[1] Amer Univ Beirut, Med Ctr, Dept Internal Med, Div Endocrinol, Beirut, Lebanon
来源：
ENDOCRINOLOGIST | 2009年 / 19卷 / 01期
关键词：
endocrinologic diseases; hemoglobinopathies; blood transfusion; SICKLE-CELL-DISEASE; BETA-THALASSEMIA MAJOR; IRON CHELATION-THERAPY; BONE-MINERAL DENSITY; GONADAL-FUNCTION; THYROID-FUNCTION; CHILDREN; GROWTH; PREVALENCE; AGE;
D O I：
10.1097/TEN.0b013e318194122e
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
Despite the improvement in chelating therapy, endocrinologic complications are well documented in patients with hemoglobinopathies requiring frequent and recurrent blood transfusion. The most common e findings are delayed puberty and growth failure. Less commonly seen are bone loss, hypothyroidism, and hyperglycemia. In this review, we will explore these complications and discuss management strategies.
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页码：44 / 47
页数：4
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