Displaying all 9 publications

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  1. TASKER PW
    Trans R Soc Trop Med Hyg, 1955 Sep;49(5):478-82.
    PMID: 13267915
    Matched MeSH terms: Anemia, Hypochromic/epidemiology*
  2. Loh TT, Chang LL
    PMID: 7403941
    Non-haemoglobin liver iron was estimated in 275 presumably normal individuals from Kuala Lumpur and Singapore at necropsy. Liver Iron concentrations were highest during the first two years after birth but declined sharply during childhood. They then rose gradually and reached a value of 20 mg/100gm in adult males. Liver iron concentrations of childbearing women remained low and it was only after menopause that values in women rose to those of males. Liver iron stores increased with age to a plateau of about 300 mg in adults, suggesting that this value may represent the adult size for liver iron store. Among the three major ethnic groups in Malaysia and Singapore, Chinese, being in a better socio-eonomic class, had larger liver iron stores. The median liver iron concentrations of Malaysians and Singaporeans, on the whole, were lower than those reported from western populations and as many as 35 per cent of the women were in a subclinical state of iron deficiency.
    Matched MeSH terms: Anemia, Hypochromic/epidemiology
  3. Khor GL
    Med J Malaysia, 1988 Dec;43(4):318-26.
    PMID: 3241597
    Matched MeSH terms: Anemia, Hypochromic/epidemiology*
  4. Kandiah M, Lee M, Ng TK, Chong YH
    J Trop Pediatr, 1984 02;30(1):23-9.
    PMID: 6429349 DOI: 10.1093/tropej/30.1.23
    Matched MeSH terms: Anemia, Hypochromic/epidemiology
  5. Ong HC
    J Trop Med Hyg, 1974 Jan;77(1):22-6.
    PMID: 4811560
    Matched MeSH terms: Anemia, Hypochromic/epidemiology
  6. Osman HA, Hamid MMA, Ahmad RB, Saleem M, Abdallah SA
    BMC Res Notes, 2020 Feb 10;13(1):65.
    PMID: 32041645 DOI: 10.1186/s13104-020-4933-5
    OBJECTIVE: Alpha-thalassemia is a genetic disorder characterized by deletions of one or more α globin genes that result in deficient of α globin chains reducing haemoglobin concentration. The study aimed to screen 97 patients with microcytosis and hypochromasia for the 3.7 and 4.2 alpha thalassemia deletion mutations.

    RESULTS: Out of 97 patients screened, only 7 were carriers for the 3.7 deletion and all patients were negative for the 4.2 deletion. The 3.7 deletion was found in Foor, Hawsa and Rezagat Sudanese tribes. In the carriers of the 3.7 deletion, Red Blood Cells and Haematocrit were significantly increased. The Red Blood Cells were 7.23 ± 0.78 × 1012/L in adult males and 7.21 ± 0.67 × 1012/L in adult females while in children were 5.07 ± 0.87 × 1012/L. The mean cell volume and mean cell haemoglobin were significantly decreased, but the mean cell haemoglobin concentration slightly decreased. Haemoglobin levels didn't revealed statistically significant decrease in adult males (11.7 ± 0.57 g/dL) and adult females (11.25 ± 0.64 g/dL), while in children were (11.6 ± 2.95 g/dL). Haemoglobin electrophoresis revealed two patients of the 3.7 and 4.2 negative were carriers for β-thalassemia. The study concluded that α3.7 deletion has frequency of 0.07 in Sudanese with hypochromasia and microcytosis.

    Matched MeSH terms: Anemia, Hypochromic/epidemiology
  7. Hibbard BM, Hibbard ED
    J Obstet Gynaecol Br Commonw, 1972 Jul;79(7):584-91.
    PMID: 5043421
    Matched MeSH terms: Anemia, Hypochromic/epidemiology
  8. Fleming AF
    Clin Haematol, 1982 Jun;11(2):365-88.
    PMID: 7042157
    Matched MeSH terms: Anemia, Hypochromic/epidemiology*
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