PedAM
Pediatric Disease Annotations & Medicines
| Disease | thalassemia |
| Symptom | C0002871|anaemia |
| Sentences | 6 |
| PubMedID- 22973867 | There remained a significant difference in anaemia among those with normal α+-thalassaemia genotype (43.0%), heterozygotes (53.5%) and homozygotes (67.7%, chi-square trend p = 0.012) (table 4). |
| PubMedID- 22413027 | Interactions of many factors that co-exist such as poor dietary intake, increased demands (e.g., growth), parasitic infections, socioeconomic causes and genetic factors (e.g., thalassaemia) may be causes of anaemia and ida. |
| PubMedID- 19912309 | The third had an intermediate alpha-thalassaemia with considerable anaemia caused by an as yet unknown polyadenylation site (aataaa>aataac) mutation in combination with a common rw deletion masked by a common hb c beta6(a3)glu-->lys heterozygosity. |
| PubMedID- 24025420 | Third, as the samples were submitted only for α thalassaemia screening, other causes of microcytic anaemia such as iron deficiency were not determined. |
| PubMedID- 22089611 | The presence of anaemia due to alpha-thalassaemia does not require any treatment in general3. |
| PubMedID- 24431329 | Haemoglobinopathy workup revealed no clinically relevant haemoglobinopathy (normal hb-electrophoresis, normal hba, hbf, hba2), but genetic data (see below) and the microcytic hypochromic anaemia were compatible with α thalassaemia trait (genotype –/αα). |
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