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Prevalence and diagnostic dilemma of chromosomal abnormalities in the Niger Delta area of Nigeria; Is prenatal diagnosis worthwhile?


Mkpe Abbey
Boma Awoala West
Simeon Chijioke Amadi
Olufemi Adebari Oloyede
Faithwin Horsfall
Esther Ijeoma Nonye-Enyidah
Kenneth Eghuan Okagua
Ngozi Joseph Kwosah
Paul Ledee Kua
Rose Sitonma Iwo-Amah
Uduak Solomon Ocheche
Chidiebere Nwakanma Ononuju
Nimi Ngo Briggs
Basil Omiebi Altraide
Leesi Sapira-Ordu
Nestor Inimgba

Abstract

Background: Early detection of increasing numbers of cases of chromosomal abnormalities (aneuploides) at the Rivers State
University Teaching Hospital (RSUTH) in the Niger Delta will enhance appropriate counseling of patients and early
termination of the affected pregnancies. The study aimed to ascertain the prevalence of aneuploides at the RSUTH and to
determine the necessity for early prenatal diagnosis in the Niger Delta.
Methodology: This was a prospective cross-sectional study carried out over a three-year period (01/01/2018 – 01/01/2021) at
the RSUTH, Nigeria. Newborn babies delivered at 28 weeks and above were assessed at birth for the phenotypes of
aneuploidy and associated birth defects. A convenient sampling method was used to recruit all the babies with chromosomal
abnormalities and their mothers. Data including that of socio-demographic, obstetric characteristics, and the fetuses were taken
and analyzed using Statistical Package for Social Sciences Version 23 (SPSS version 23). Quantitative variables were
summarized using means and standard deviation while qualitative variables were expressed as frequencies and proportions.
Results: The total number of babies that were delivered by the 5868 participants in the study was 6078, out of which 10 cases
of aneuploides were identified – 3 cases of trisomy 18 and 7 cases of Trisomy 21. The prevalence of chromosomal
abnormalities at birth at the RSUTH was 0.165% of the total births, 1:2000 and 1:654 for T18 and T21 respectively. 1:654
mothers had babies with chromosomal abnormalities, 1:2000 and 1:833 for T18 and T21 respectively.
Conclusion: The prevalence of chromosomal abnormalities at birth at the RSUTH of 0.165% represented a gross
underestimation because the diagnosis was based on the outward phenotypical appearance of the neonates and it was made not
from babies delivered at 20 weeks and above as practiced in Europe and other countries, but from 28 weeks. Prenatal diagnosis
was therefore highly recommended in the Niger Delta.


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eISSN: 2229-774X
print ISSN: 0300-1652