Abstract
Lissencephaly, a developmental malformation characterized by absence of sulci, may be suggested in dysmorphic or epileptic infants. Real time ultrasonographic findings correlated with typical electroencephalographic abnormalities establish the diagnosis.
Similar content being viewed by others
References
Bielchowsky M (1923–24) Über die Oberflächengestaltung des Grosshirnmantels bei Pachygyrie, Mikrogyrie und bei normaler Entwicklung. J Psych Neurol 30: 29
Diexer H, Edwards RH, Zu Rhein G, Chou SM, Hartman HA, Optiz JM (1969) The lissencephaly syndrome. Birth Defects 5: 53
Dobyns WB, Stratton RF, Parke JT, Greenberg F, Nussbaum RL, Ledbetter DH (1983) Mieller-Dieker syndrome, lissencephaly and monosomy 17 p. J Pediatr 102: 552
Dulac O, Plouin P, Perulli L, Diebler C, Arthuis M, Jalin C (1983) Aspects électroencéphalographiques de l'agyrie-pachygyrie classique. Rev Electroencephalogr Neurophysiol Clin 13: 232
Ohno K (1979) Lissencephaly on computed tomography. J Comput Assist Tomogr 3: 92
Garcia CA, Dunn D, Trevor R (1978) The lissencephaly (agyrie) Syndrome in Siblings. Arch Neurol 35: 608
Dobyns WB, Stratton RF, Parke JT, Greenberg F, Nussbaum RL, Ledbetter DH (1983) Miller-Dieker syndrome, lissencephaly and monosomy 17 p. J Pediatr 102: 552
Couture A, Cadier L (1983) Echographie cérébrale par voie transfontanellaire. Edition Vigot, p 241
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Motte, J., Gomes, H., Morville, P. et al. Sonographic diagnosis of lissencephaly. Pediatr Radiol 17, 362–364 (1987). https://doi.org/10.1007/BF02396608
Received:
Accepted:
Issue Date:
DOI: https://doi.org/10.1007/BF02396608