Search Results - "Gnamey, D"

Aplasia cutis congenita associated with Goltz syndrome in a male neonate by Gnamey, D K, Koffi, K S, Nagalo, K, Guedenon, K M, Akakpo-Numado, G K, Balaka, B, Tatagan-Agbi, K, Atakouma, D Y

“…Here we report the association of giant aplasia cutis congenita in a newborn black male with Goltz syndrome. The cutis aplasia defect is extensive and…”
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Dandy-Walker syndrome with postaxial polydactyly associated with facial dysmorphism and bone abnormalities by Gnamey, D K, Koffi, K S

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Wolf Hirshhorn syndrome in a case of ring chromosome 4: phenotype and molecular cytogenetic findings by Laleye, A, Alao, M J, Adjagba, M, Hans, C, Delneste, D, Gnamey, D K, Ayivi, B, Darboux, R B

“…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…”
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Primary autosomal recessive microcephaly: a novel clinical phenotype by Gnamey, D K, Alao, M J, Agbodjan-Djossou, O, Koffi, S K

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Morbi-mortalité des enfants de 0 à 15 ans hospitalisés en pédiatrie à l’hôpital de Bè (Togo) en 2005 by Koffi, K.S, T.Guédéhoussou, Djadou, K.E., Gbadoé, A.D., J.Guédénon, Gnamey, D.K., Atakouma, D.Y.

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Anhidrotic ectodermal dysplasia as autosomal recessive trait in one Ewe isolate at Togo (33 cases in 23 families) by Gnamey, D-K, Kpégba, A-K-G

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Dysplasie ectodermique anhidrotique à transmission autosomique récessive dans un isolat Ewé au Togo. Rapport de 33 cas dans 23 familles by Gnamey, D.-K, Kpégba, A.-K.-G

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Le syndrome d'Apert : à propos d'une observation by DOUTETIEN, C, LALEYE, A, TCHABI, S, BIAOU, O, LAWANI, R, DEGUENON, J, DARBOUX, R, GNAMEY, D, BASSABI, S. K

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Hybridation in situ en fluorescence et trisomie 13 en mosaïque : un exemple de difficultés de prise en charge des maladies génétiques au Togo by Gnamey, D.K., Dovi-Akué, J.P., Darboux, R.B., Laleye, A., Adjenou, P., Adanlete, F.

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Morbidity and mortality of children 0-15 years old hospitalized in pediatric unit at the hospital of Bè (Togo) in 2005 by Koffi, K S, Guédéhoussou, T, Djadou, K E, Gbadoé, A D, Guédénon, J, Gnamey, D K, Atakouma, D Y

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Profil infectieux du nouveau-né dans un service de pédiatrie d'un CHR au Togo by AGBERE, A. D, BAYILABOU, K, GNAMEY, D. K, KESSIE, K, ASSIMADI, K

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In situ fluorescent hybridization and trisomy 13 mosaicism: an example of the difficulty in managing genetic diseases in Togo by Gnamey, D K, Dovi-Akué, J P, Darboux, R B, Laleye, A, Adjenou, P, Adanlete, F

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Apert's syndrome: a case report by Doutetien, C, Laleye, A, Tchabi, S, Biaou, O, Lawani, R, Deguenon, J, Darboux, R, Gnamey, D, Bassabi, S K

“…Apert's syndrome is a type of acrocephalosyndactylia that is from part of the great group of craniofacial synostoses. It is characterized by craniofacial…”
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The fingerprint diagnosis of Poland's syndrome without syndactylia. A study of four cases by Gnamey, D

“…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…”
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Huntington disease in a large family in southern Togo by Grunitzky, E K, Gnamey, D R, Nonon, S A, Balogou, A

“…We report the clinical manifestations and the family in a large family in Southern Togo in which Huntington's disease is known to exist for the past 6…”
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Infectious profile of the newborn in a pediatric unit in a regional hospital center in Togo by Agbéré, A D, Bayilabou, K, Gnamey, D K, Kessie, K, Assimadi, K

“…In one year 106 suspect cases of neo-natal infection were admitted to the pediatric ward of CHR in Kara. The principal elements of diagnosis (slow labor,…”
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Poland's syndrome. Etiological consideration by Gnamey, D

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A dominant syndrome associated with polysyndactyly, spatule thumb, facial abnormalities, and mental retardation. (A particular form of Noack's acrocephalosyndactylia) by Gnamey, D, Farriaux, J P

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Camptomelic dysplasia. Apropos of a case by Gnamey, D K, Eynard, J P

“…A new case of campomelic dysplasia is reported, probably the first in Africa, with several remarkable points which might suggest an hypothetic embryopathy…”
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In situ fluorescent hybridization and trisomy 13 mosaicism: an example of the difficulty in managing genetic diseases in Togo by Gnamey, D K, Dovi-Akué, J P, Darboux, R B, Laleye, A, Adjenou, P, Adanlete, F

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