Zinc deficiency is a common nutritional problem in adult sickle-cell disease (SCD) patients. Hyperzincuria and increased requirement of zinc due to continued hemolysis in SCD are probable bases for zinc deficiency in these patients. Zinc deficiency affects adversely T-helper 1 (TH 1 ) functions and
Zinc supplementation treatment of growth retardation and hypogonadism in sickle cell patients
โ Scribed by George Brewer
- Publisher
- John Wiley and Sons
- Year
- 1981
- Tongue
- English
- Weight
- 261 KB
- Volume
- 10
- Category
- Article
- ISSN
- 0361-8609
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๐ SIMILAR VOLUMES
## Abstract Previously, we have documented primary testicular failure in adult male subjects with sickle cell anemia. We have also reported the occurrence of zinc deficiency and suggested that androgen deficiency may be related to zinc deficiency in such patients. In this study, we present data wit
Using homocysteine as a functional marker, we determined optimal folic acid, vitamin B 12 , and vitamin B 6 dosages in 21 pediatric sickle cell disease (SCD) patients (11 HbSS, 10 HbSC;(7)(8)(9)(10)(11)(12)(13)(14)(15)(16). Daily supplements of folic acid (400, 700, or 1,000 lg), vitamin B 12 (1, 3,