Zobrazeno 1 - 10
of 28
pro vyhledávání: '"M, Adjagba"'
Autor:
A. Sonou, M. Hounkponou, L. Codjo, P. M. Adjagba, C. Houehanou, H. Dohou, S. Assani, Y. Tchabi, M. Houenassi
Publikováno v:
Case Reports in Cardiology, Vol 2017 (2017)
Persistent left superior vena cava (LSVC) is a rare congenital anomaly. Its prevalence in the general population is 0.1 to 0.5%. LSVC is 5 times rarer when accompanied by an absence of the right superior vena cava (RSVC). We present the case of a 54-
Externí odkaz:
https://doaj.org/article/f73c40c475fa43ac93051e9ab6ac20d1
Autor:
D M, Houénassi, A, Sonou, M, Hounkponou, P M, Adjagba, M, Ahodakin, W, Gandji, Shm, Dohou, L, Codjo, J, Ezin-Houngbé
Publikováno v:
Annales de cardiologie et d'angeiologie. 71(3)
The aim was to study the psycho-social experiences and quality of life (QOL) of pacemaker patients at the National Teaching Hospital Hubert Koutoukou Maga in Cotonou.A descriptive cross-sectional observational study was performed in 2017 and included
Autor:
A, Sonou, P M, Adjagba, M, Hounkponou, L, Codjo, C, Houéhanou-Sonou, S, Assani, T, Yessoufou, J, Sacca, M, Houénassi
Publikováno v:
Annales de cardiologie et d'angeiologie. 66(1)
We report the case of a patient with pacemaker who presented chest pain during exercise followed by fainting. He has a history of arterial hypertension and diabetes. The initial examination was normal; the ventricular stimulation threshold was 1.125
Akademický článek
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Publikováno v:
Journal of Genetic Disorders & Genetic Reports.
Ring 9 Chromosome Syndrome in Black African Infant Ring chromosomes are rare entities, usually associated with phenotypic abnormalities in correlation with the loss of genetic material. Ring 9 chromosome syndrome is very rare. The majority of reporte
Autor:
A, Laleye, B, Awede, B, Agboton, S, Azonbakin, O, Biaou, G, Sagbo, M, Adjagba, M P, Audrezet, C, Ferec, R, Darboux
Publikováno v:
Genetic counseling (Geneva, Switzerland). 23(4)
Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary kidney disease, but poorly studied in Africa. Its frequency in the University Clinic of Nephrology and Hemodialysis of Cotonou during the ten last years was 7 cases pe
Autor:
A, Laleye, M J, Alao, G, Gbessi, M, Adjagba, M, Marche, I, Coupry, I, Redonnet-Vernhet, S, Lepreux, B, Ayivi, R B, Darboux, D, Lacombe, B, Arveiler
Publikováno v:
Genetic counseling (Geneva, Switzerland). 19(2)
Familial Tumoral Calcinosis (FTC) is a rare autosomal recessive disorder of the phosphocalcic metabolism caused by mutations in the FGF23 or GALNT3 genes. We have identified a Beninese family in which two brothers present FTC caused by a homozygous A
Wolf Hirshhorn syndrome in a case of ring chromosome 4: phenotype and molecular cytogenetic findings
Publikováno v:
Genetic counseling (Geneva, Switzerland). 17(1)
Ring chromosome 4 associates concomitant loss of the telomeric 4p and 4q regions and leads to variable clinical manifestations depending on the size of the deleted chromosomal material. We report on a patient with ring chromosome 4, showing the Wolf-
Akademický článek
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