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Acromelic Frontonasal "Dysplasia": Further Delineation of a Subtype with Brain Malformation and Polydactyly (Toriello Syndrome)
Verloes, Alain; Gillerot, Y.; Walczak, E. et al.
1992In American Journal of Medical Genetics, 42 (2), p. 180-3
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Abstract :
[en] We report on a stillborn boy with frontonasal malformation (Sedano-Jirasek type D-DeMyer type I), associated with encephalocoele, occipital meningocele and preaxial polydactyly of the feet. This form of frontonasal dysplasia was documented previously in a few other cases with various combinations of postaxial polydactyly, tibial hypoplasia, epibulbar dermoid, occipital encephalocoele, corpus callosum agenesis and Dandy-Walker malformation. Most cases are sporadic.
Disciplines :
Genetics & genetic processes
Author, co-author :
Verloes, Alain ;  Université de Liège - ULiège > Génétique générale et humaine
Gillerot, Y.
Walczak, E.
Van Maldergem, Lionel ;  Centre Hospitalier Universitaire de Liège - CHU > Génétique
Koulischer, Lucien ;  Université de Liège - ULiège > Relations académiques et scientifiques (Médecine)
Language :
English
Title :
Acromelic Frontonasal "Dysplasia": Further Delineation of a Subtype with Brain Malformation and Polydactyly (Toriello Syndrome)
Publication date :
15 January 1992
Journal title :
American Journal of Medical Genetics
ISSN :
0148-7299
Publisher :
Wiley-Liss Inc, United States - New Jersey
Volume :
42
Issue :
2
Pages :
180-3
Peer reviewed :
Peer Reviewed verified by ORBi
Available on ORBi :
since 14 February 2011

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