Agyria-pachygyria and agenesis of the corpus callosum: Autosomal recessive inheritance with neonatal death

被引:7
作者
Sztriha, L
Al-Gazali, L
Dawodu, A
Bakir, M
Chandran, P
机构
[1] United Arab Emirates Univ, Fac Med & Hlth Sci, Dept Pediat, Al Ain, U Arab Emirates
[2] Al Ain Hosp, Dept Pediat, Al Ain, U Arab Emirates
[3] Al Ain Hosp, Dept Radiol, Al Ain, U Arab Emirates
关键词
D O I
10.1212/WNL.50.5.1466
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
We report three neonates, one boy and two girls, born to an inbred Arab family who had cortical dysplasia, probably agyria-pachygyria, and agenesis of the corpus callosum. All had asphyxia, intractable seizures, and increased muscle tone at birth and died in the neonatal period. Congenital microcephaly or dysmorphic features were absent. Cytogenetic abnormality, metabolic disorder, and intrauterine infection were excluded. These cases suggest a new cerebral dysgenesis syndrome with autosomal recessive inheritance.
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页码:1466 / 1469
页数:4
相关论文
共 10 条
[1]   METABOLIC DISORDERS OF EMBRYOGENESIS [J].
BROWN, GK .
JOURNAL OF INHERITED METABOLIC DISEASE, 1994, 17 (04) :448-458
[2]   Cobblestone lissencephaly with normal eyes and muscle [J].
Dobyns, WB ;
Patton, MA ;
Stratton, RF ;
Mastrobattista, JM ;
Blanton, SH ;
Northrup, H .
NEUROPEDIATRICS, 1996, 27 (02) :70-75
[3]   AGENESIS OF THE CORPUS-CALLOSUM AND GYRAL MALFORMATIONS ARE FREQUENT MANIFESTATIONS OF NONKETOTIC HYPERGLYCINEMIA [J].
DOBYNS, WB .
NEUROLOGY, 1989, 39 (06) :817-820
[4]   CAUSAL HETEROGENEITY IN ISOLATED LISSENCEPHALY [J].
DOBYNS, WB ;
ELIAS, ER ;
NEWLIN, AC ;
PAGON, RA ;
LEDBETTER, DH .
NEUROLOGY, 1992, 42 (07) :1375-1388
[5]   LISSENCEPHALY AND OTHER MALFORMATIONS OF CORTICAL DEVELOPMENT - 1995 UPDATE [J].
DOBYNS, WB ;
TRUWIT, CL .
NEUROPEDIATRICS, 1995, 26 (03) :132-147
[6]  
Friede R. L., 1989, DEV NEUROPATHOLOGY, P330
[7]   Lissencephaly with extreme cerebral and cerebellar hypoplasia. A magnetic resonance imaging study [J].
Kroon, AA ;
Smit, BJ ;
Barth, PG ;
Hennekam, RCM .
NEUROPEDIATRICS, 1996, 27 (05) :273-276
[8]   Association of cerebral dysgenesis and lactic acidemia with X-linked PDH E1 alpha subunit mutations in females [J].
Otero, LJ ;
Brown, GK ;
Silver, K ;
Arnold, DL ;
Matthews, PM .
PEDIATRIC NEUROLOGY, 1995, 13 (04) :327-332
[9]  
SHEVELL MI, 1994, PEDIATR NEUROL, V12, P350
[10]   ELECTROPHYSIOLOGICAL AND TC-99M-HMPAO-SPECT STUDIES IN MENKES DISEASE [J].
SZTRIHA, L ;
JANAKY, M ;
KISS, J ;
BUGA, K .
BRAIN & DEVELOPMENT, 1994, 16 (03) :224-228