Abstract
DEL is the weakest RhD-positive phenotype that commonly mistyped as RhDnegative. It may induce alloimmunization when transfused to RhD-negative recipients. Serologically, it can only be detected via adsorption-elution test. In Malaysia, few data exist regarding DEL phenotype. The objective of this study was to detect DEL phenotype in RhD-negative blood using adsorption-elution technique and Sequence Specific Primer-Polymerase Chain Reaction (SSP-PCR). A total of 43 RhD-negative blood samples were collected from Pusat Darah Negara. Rh phenotype for each sample was tested. Heat elution by incubation at 56°C for 10 minutes were implemented. Indirect Antiglobulin Test against Rh(+) cells and Rh(-) cells were completed on the eluates and last wash supernatant. Then, identification of DEL carrying RHD1227A was performed via SSP-PCR. Rh-phenotype identified were ccee with 79.07%, Ccee with 13.95%,4.65% of ccEe phenotype and CCee phenotype with only 2.33%. One (2.33%) out of 43 samples was identified as DEL phenotype carrying RHDI227A allele when tested using SSP-PCR but none was identified from adsorption-elution. SSP-PCR was more sensitive and specific compared to adsorption-elution test. Hence, implementation of SSP-PCR for efficient DEL phenotypes typing is highly recommended.
Metadata
Item Type: | Thesis (Degree) |
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Creators: | Creators Email / ID Num. Maswan, Nor Elizatul Izzati UNSPECIFIED |
Subjects: | R Medicine > RB Pathology > Clinical pathology. Laboratory technique > Examination of the blood |
Divisions: | Universiti Teknologi MARA, Shah Alam > Faculty of Health Sciences |
Programme: | Bachelor of Medical Laboratory Technology |
Keywords: | DEL phenotype, Rh negative, heat elution, RHD1227A, Sequence Specific Primer-Polymerase Chain Reaction (SSP-PCR). |
Date: | 2015 |
URI: | https://ir.uitm.edu.my/id/eprint/28031 |
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