Reporting a rare RH phenotype D-
نویسندگان
چکیده
منابع مشابه
A family study of an extremely rare Rh-Hr variant (-D-/-D-) in two generations.
A rare variant (-D-/-D-) in two generations due to consanguineous marriage was reported. The propositus (T.M., 27 years of age) delivered her second baby who suffered from severe jaundice. She had agglutinin of titer 1:64 in saline and 1:1,024 in Coomb's test against red cells of her husband (CDe/cDE). Family study revealed that T.M.'s father and his two siblings were grouped as -D-/-D-. Each o...
متن کاملگزارش یک مورد فنوتیپ نادر Rh--D: یک گزارش مورد
Background and Objective: Of all blood group systems, RH is one of the most important blood groups, which its compatibility is one of the essential principals of transfusion. Two genes (RhD and RhCE) locate on chromosome 1, and encode the Rh proteins. RhD is an immunogenic antigen. We describe a rare Rh phenotype D-- in this report. Case Report: A forty- nine- year- old man, who receiv...
متن کاملSignificance of serological monitoring in a Bombay Rh (D) negative phenotype pregnant woman: a case report.
A 32 year old Indian female was referred to our hospital at 32 weeks of gestation because of difficulty in blood group determination and further antenatal care. The results of cell and serum grouping of her blood sample were suggestive of Bombay (O(h)) Rh (D) negative phenotype. An indirect antiglobulin test (IAT) using a pool of red cells from two Bombay Rh (D) positive blood donors gave negat...
متن کاملIdentification of a partial internal deletion in the RH locus causing the human erythrocyte D--phenotype.
The D--phenotype of the human erythrocyte is a genetic variant of the Rh blood group system associated with the expression of D but not C, c, E, and e (designated non-D) antigens. In this report, we characterize the structure and expression of Rh polypeptide genes in two D--homozygotes of Italian origin. Southern blot analysis detected a gross deletion in their genomic DNA that correlated with ...
متن کاملIdentification of First Patient with Rh null Phenotype in Southeast Iran
Background and Aims: Rhnull, with an estimated incidence of one per 6,000,000 individuals, is an extremely rare disorder with an autosomal recessive pattern of inheritance that is more common in societies with a high rate of consanguinity. Materials and Methods: In this study, we report the first case with Rhnull, a blood group phenotype in southeast Iran, which was diagnosed during pretransf...
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ژورنال
عنوان ژورنال: Journal of Applied Hematology
سال: 2015
ISSN: 1658-5127
DOI: 10.4103/1658-5127.155184