Near-total absence of the cerebellum

被引:20
作者
Gardner, RJM
Coleman, LT
Mitchell, LA
Smith, LJ
Harvey, AS
Scheffer, IE
Storey, E
Nowotny, MJ
Sloane, RA
Lubitz, L
机构
[1] Royal Childrens Hosp, Victorian Clin Genet Serv, Melbourne, Vic 3052, Australia
[2] Royal Childrens Hosp, Dept Radiol, Melbourne, Vic 3052, Australia
[3] Australian & Repatriat Ctr, Dept Radiol, Melbourne, Vic, Australia
[4] Royal Childrens Hosp, Dept Neurol, Melbourne, Vic 3052, Australia
[5] Austin & Repatriat Ctr, Dept Neurol, Melbourne, Vic, Australia
[6] Monash Univ, Dept Neurosci, Melbourne, Vic 3004, Australia
[7] Warragul Hosp, Dept Pediat, Warragul, Australia
[8] Royal Childrens Hosp, Dept Pediat, Melbourne, Vic 3052, Australia
关键词
cerebellar malformation; cerebellar agenesis; cerebellar absence; pontocerebellar hypoplasia;
D O I
10.1055/s-2001-13882
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
We report five cases of near-total absence of the cerebellum with accompanying pontine hypoplasia. The cerebellar remnant in each case comprised only antero-superior masses, the posterior fossa being otherwise fluid filled. Three of these patients, two teenagers and an infant, presented a fairly consistent clinical and neuroradiological phenotype, and a few similar cases are recorded in the literature. The cerebellar remnant was irregular and asymmetrical, and no ventral pontine prominence was discernible, In at least the older two, cerebellar motor functions were not greatly compromised, and intellectual handicap was of a mild degree. We propose that these cases represent a distinct entity of "near-total absence of the cerebellum with flat ventral pens, and relatively mild clinical affection". All cases have been sporadic, implying that the risk of recurrence within a family may be low. Quite different clinical pictures, of considerably greater severity, are demonstrated in the remaining two cases. One had pontocerebellar hypoplasia type 2, while the other had a complex cerebellar and cerebral malformation.
引用
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页码:62 / 68
页数:7
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