论文信息 - Homozygous Beta Thalassaemia and Pregnancy

Homozygous Beta Thalassaemia and Pregnancy

Summary: Pregnancy complicating homozygous beta thalassaemia is a rare entity. Two cases are described, I of which was further complicated by thrombocytopenia due to secondary hyperslenism. These cases are discussed in the light of current management of homozygous haemoglobinopathies.

E. Grech | C. Ventura | L. J. P. Silva

[1] E. Schwartz,et al. Clinical features of thalassemia. , 1980, Pediatric clinics of North America.

[2] D. Nathan,et al. New approaches to the transfusion management of thalassemia , 1980 .

[3] D. Nathan,et al. New approaches to the transfusion management of thalassemia. , 1980, Blood.

[4] E. Schwartz,et al. Iron chelation therapy with deferoxamine in Cooley anemia. , 1978, The Journal of pediatrics.

[5] J. Fisher. Erythropoietin: pharmacology, biogenesis and control of production. , 1972, Pharmacological reviews.

[6] R. Perkins. Inherited disorders of hemoglobin synthesis and pregnancy. , 1971, American journal of obstetrics and gynecology.

[7] J. Jepson,et al. Erythropoietin in plasma and urine during human pregnancy. , 1969, Canadian Medical Association journal.

[8] R. Heys. CHILD BEARING AND IDIOPATHIC THROMBOCYTOPENIC PURPURA , 1966 .

[9] I. Wolman. Transfusion Therapy in Cooley's Anemia: Growth and Health as Related to Long‐Range Hemoglobin Levels. A Progress Report , 1964, Annals of the New York Academy of Sciences.