Update on Thalassemia: Clinical care and Complications  

Oleh:

Cunningham, Melody J

Jenis: Article from Journal - ilmiah internasional
Dalam koleksi: Pediatric Clinics of North America vol. 55 no. 02 (Apr. 2008), page 447.
Topik: Pediatric Hematology

Ketersediaan

Perpustakaan FK Nomor Panggil: P13.K.2008.02 Non-tandon: 1 (dapat dipinjam: 0) Tandon: tidak ada

Lihat Detail Induk

Isi artikel

ß-Thalassemia, originally named Cooley anemia, is an inherited blood disease. Various types of thalassemia are inherited anemias caused by mutations at the globin gene loci on chromosomes 16 and 11, affecting the production of a- or ß-globin protein, respectively. The combination of early diagnoses, improvements in monitoring for organ complications, and advances in supportive care have enabled many patients who have severe thalassemia syndromes to live productive, active lives well into adulthood.

Opini Anda

Klik untuk menuliskan opini Anda tentang koleksi ini!

Kembali