Regional variation in the prevalence of sickle cell anemia (HBSS) across Africa.

Regional variation in the prevalence of sickle cell anemia (HBSS) across Africa.

<p>Map created by authors using shapefiles from GADM (Database of Global Administrative Areas, version 4.1, <a href="https://www.gadm.org" target="_blank">www.gadm.org</a>).</p>

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Detaylı Bibliyografya
Yazar: Bwambale Jonani (21156747) (author)
Diğer Yazarlar: Emmanuel Charles Kasule (21156750) (author), Bwire Roman Herman (21168941) (author), Joel Fredrick Arturo (21156756) (author), Mwesigwa Calvin Mugambwa (22683322) (author), Ssebulime Stephen (21156771) (author), John Bosco Mundaka (20309196) (author), Richard Kwizera (606632) (author), Gerald Mboowa (770601) (author), Felix Bongomin (5081681) (author)
Baskı/Yayın Bilgisi: 2025
Konular:
Biotechnology
Science Policy
Infectious Diseases
Biological Sciences not elsewhere classified
three decades despite
systematically searched pubmed
sickle cell anemia
electrophoretic techniques predominated
21 %– 8
1994 &# 8211
improved diagnostic accessibility
southern africa showed
sensitivity analysis showed
central africa showed
74 %; p
significant genetic disorder
including geographic region
08 %– 1
analysis </ p
2 </ sup
males 2
diagnostic method
xlink ">
temporal variations
systematic review
subgroup analyses
study variability
study design
specific interventions
significantly moderated
research output
remained stable
quality assurance
quality assessments
prediction interval
marginally significant
logit transformation
google scholar
fold increase
findings highlight
examine regional
continued surveillance
comprehensive data
children exhibited
cases ).
care technologies
base databases
african populations
91 %.
88 %),
839 participants
694 ).
65 %)
6 %).
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