Zobrazeno 1 - 10
of 59
pro vyhledávání: '"D Gnamey"'
Publikováno v:
Journal de la Recherche Scientifique de l’Université de Lomé; Vol 11, No 2 (2009): Serie D
Les auteurs ont rapporte un nouveau cas de malformation de vessie chez un nouveau-ne de 32 semaines ; les problemes de diagnostic et de prise en charge ont ete repertories et discutes a la vue des donnees de la litterature. Mots cles : Extrophie vesi
Autor:
C, Doutetien, A, Laleye, S, Tchabi, O, Biaou, R, Lawani, J, Deguenon, R, Darboux, D, Gnamey, S K, Bassabi
Publikováno v:
Journal francais d'ophtalmologie. 26(7)
Apert's syndrome is a type of acrocephalosyndactylia that is from part of the great group of craniofacial synostoses. It is characterized by craniofacial dysmorphia and syndactylia on hands and feet, which differentiates it from Crouzon's disease. It
Publikováno v:
Medecine tropicale : revue du Corps de sante colonial. 63(2)
The purpose of the study was to identify predisposing factors for acute hemolysis and post-hemolytic renal failure in children with glucose-6-phosphate dehydrogenase deficiency (G6PD). Any child presenting hemoglobinuria during the study period was p
Publikováno v:
Archives francaises de pediatrie. 33(2)
Kniest's disease (spondylo-epiphyseal dysplasia) was recently described by Maroteaux and Spranger. A second familial case is studied. Transmission of the disease occurred as a dominant trait.
Publikováno v:
Archives francaises de pediatrie. 31(1)
Publikováno v:
Journal de genetique humaine. 25(4)
The authors studied 7 patients with type C brachydactyly and 5 patients with type E brachydactyly. 1. In the C type cases the findings were as follows: a) frequency of anomalies of the digital folds (a fold of the digital flexion); b) frequency of si
Autor:
D, Gnamey
Publikováno v:
Lille medical : journal de la Faculte de medecine et de pharmacie de l'Universite de Lille. 19(9)
Publikováno v:
Pediatrie. 30(2)
Publikováno v:
Pediatrie. 30(3)
Autor:
D, Gnamey
Publikováno v:
Journal de genetique humaine. 24(3)
The author studied the fingerprints of four children (three girls and one boy) aged from five months to eleven years who were suffering from Poland's syndrome without syndactylia. He recorded the following peculiarities: a distal triradius in t" (in