Haemolytic disease of the newborn
Journal of the Faculty of Medicine-Baghdad. 1993; 35 (4): 559-564
in English
| IMEMR
| ID: emr-28510
ABSTRACT
Ninty two patients were included in this study, 6 Groups -were identified. ABO HDN [Group I, n=38]. Rh HDN [Group H, n=17], HDN due to G6PD deficiency [Group Ill. n=23], HDN of undetermined aetiology [Group IV, n=10], Hereditary spherocytosis [Group V, n= 1] and [Group VI, n=5] HDN due to combined pathology. Detailed clinical, haematological and serological tests were studied and compared between different groups and with other studies
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Index:
IMEMR (Eastern Mediterranean)
Main subject:
Rh Isoimmunization
/
Spherocytosis, Hereditary
/
Bilirubin
/
Blood Group Incompatibility
/
Infant, Newborn
/
Coombs Test
Limits:
Female
/
Humans
/
Male
Language:
English
Journal:
J. Fac. Med.-Baghdad
Year:
1993
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