Polymicrogyria and motor neuropathy in Micro syndrome

Neuropediatrics

Volumn 31, Issue 4, 2000, Pages 218-221

  Nassogne, M C ^a   Henrot, B ^a   Saint Martin, C ^a   Kadhim, H ^a   Dobyns, W B ^b   Sebire, G ^a  

^a CLINIQUES UNIVERSITAIRES SAINT LUC   (Belgium)

^b UNIVERSITY OF CHICAGO   (United States)

Author keywords

Cataract; Gyral abnormalities; Microcephaly; Microphthalmia

Indexed keywords

ARTICLE; CASE REPORT; CHILD; CONGENITAL CATARACT; FACE DYSMORPHIA; HUMAN; MALE; MENTAL DEFICIENCY; MICRO SYNDROME; MICROCEPHALY; MICROGYRIA; MICROPHTHALMIA; MOTOR NEUROPATHY; NEUROLOGIC DISEASE; PRIORITY JOURNAL; PSYCHOMOTOR RETARDATION;

BRAIN; CHILD, PRESCHOOL; DEMYELINATING DISEASES; HUMANS; MAGNETIC RESONANCE IMAGING; MALE; MICROCEPHALY; NEURAL CONDUCTION; PERIPHERAL NERVOUS SYSTEM DISEASES; PSYCHOMOTOR DISORDERS;

EID: 0033771455     PISSN: 0174304X     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2000-7463     Document Type: Article

References (10)

1. Cerebro-oculo-facio-skeletal (COFS) syndrome: The variability of presenting symptoms as a manifestation of two subtypes?
2. Neuropathological findings in eight children with cerebro-oculo-facio-skeletal (COFS) syndrome
3. Microcephaly, microphthalmia, congenital cataract, optic atrophy, short stature, hypotonia, severe psychomotor retardation, and cerebral malformations: A second family with micro syndrome or a new syndrome?
4. A second family with Micro syndrome
5. Neuropathological findings in the cerebro-oculo-facio-skeletal (Pena-Shokeir II) syndrome
6. Cataract, motor system disorder, short stature, learning difficulties, and skeletal abnormalities: A new syndrome?
7. Autosomal recessive microcephaly, microcornea, congenital cataract, mental retardation, optic atrophy, and hypogenitalism: Micro syndrome