Integrative classification of morphology and molecular genetics in central nervous system malformations

被引:39
作者
Sarnat, HB
Flores-Sarnat, L
机构
[1] Cedars Sinai Med Ctr, Dept Pediat Neurol, Los Angeles, CA 90048 USA
[2] Cedars Sinai Med Ctr, Dept Pathol Neuropathol, Los Angeles, CA 90048 USA
[3] Univ Calif Los Angeles, Sch Med, Los Angeles, CA 90024 USA
关键词
classification; CNS malformations; axes of neural tube; holoprosencephaly; lissencephaly; cortical dysplasia; gradients of genetic expression;
D O I
10.1002/ajmg.a.20663
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We propose a scheme to classify central nervous system (CNS) malformations that integrates morphology and genetics by using patterns of genetic expression as its basis. The precise genetic mutations are not necessary to know in all cases. The premises of this classification are (1) genetic expression in the neural tube follows gradients in the axes that are established at the time of gastrulation: vertical (dorsoventral and ventrodorsal); rostrocaudal; mediolateral. (2) Overexpression in one of these gradients generally results in duplication or hyperplasia of structures, or ectopic segmental (i.e., neuromeric) expression. (a) Underexpression in a gradient generally results in hypoplasia, noncleavage in the midline of paired structures or segmental deletion of neuromeres. These gradients may also affect the formation and migration of neural crest tissue, affecting non-neural structures such as the face in the case of the mesencephalic neural crest, or induction of paraxial mesodermal in the posterior fossa. Additional criteria of the new classification allow for other genetic influences on developmental processes, such as cellular lineage, exemplified by tuberous sclerosis, and hemimegalencephaly. It is essential that the CNS be considered as a whole and classification not be regionalized, as to the cerebral cortex, because the limit of the rostrocaudal gradient may account for variability in clinical manifestations. (C) 2004 Wiley-Liss, Inc.
引用
收藏
页码:386 / 392
页数:7
相关论文
共 40 条
[1]  
BARKOVICH JA, 2000, PEDIAT NEUROIMAGING
[2]   Development of the facial midline [J].
Carstens, MH .
JOURNAL OF CRANIOFACIAL SURGERY, 2002, 13 (01) :129-187
[3]  
Casarosa S, 1999, DEVELOPMENT, V126, P525
[4]   Two rights make a wrong: human left-right malformations [J].
Casey, B .
HUMAN MOLECULAR GENETICS, 1998, 7 (10) :1565-1571
[5]  
DEMYER W, 1964, PEDIATRICS, V34, P256
[6]  
des Portes V, 1998, CELL, V92, P51
[7]   LISSENCEPHALY - A HUMAN BRAIN MALFORMATION ASSOCIATED WITH DELETION OF THE LIS1 GENE LOCATED AT CHROMOSOME-17P13 [J].
DOBYNS, WB ;
REINER, O ;
CARROZZO, R ;
LEDBETTER, DH .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1993, 270 (23) :2838-2842
[8]   Periventricular heterotopia: An X-linked dominant epilepsy locus causing aberrant cerebral cortical development [J].
Eksioglu, YZ ;
Scheffer, IE ;
Cardenas, P ;
Knoll, J ;
DiMario, F ;
Ramsby, G ;
Berg, M ;
Kamuro, K ;
Berkovic, SF ;
Duyk, GM ;
Parisi, J ;
Huttenlocher, PR ;
Walsh, CA .
NEURON, 1996, 16 (01) :77-87
[9]   Hemimegalencephaly:: Part 2.: Neuropathology suggests a disorder of cellular lineage [J].
Flores-Sarnat, L ;
Sarnat, HB ;
Dávila-Gutiérrez, G ;
Alvarez, A .
JOURNAL OF CHILD NEUROLOGY, 2003, 18 (11) :776-785
[10]  
Flores-Sarnat L, 2002, J NEUROPATH EXP NEUR, V61, P469