Aicardi syndrome in a girl with mild developmental delay, absence of epilepsy and normal EEG

Clinical Dysmorphology

Volumn 13, Issue 4, 2004, Pages 257-260

  Matlary, Arpad ^a   Prescott, Trine ^a   Tvedt, Bjørn ^a   Lindberg, Knut ^a   Server, Andres ^a   Aicardi, Jean ^b   Strømme, Petter ^a  

^a ULLEVÅL UNIVERSITY HOSPITAL   (Norway)

^b HÔPITAL ROBERT DEBRÉ   (France)

Author keywords

Aicardi syndrome; Chorioretinal lacunae; Corpus callosum agenesis; X linked dominant inheritance

Indexed keywords

AGENESIS; AICARDI SYNDROME; ARTICLE; BRAIN ATROPHY; BRAIN MALFORMATION; CASE REPORT; CHILD DEVELOPMENT; CHROMOSOME BANDING PATTERN; CHROMOSOME G BAND; CLINICAL FEATURE; CORPUS CALLOSUM; DEVELOPMENTAL DISORDER; ELECTROENCEPHALOGRAM; EPILEPSY; FEMALE; HUMAN; INTELLIGENCE QUOTIENT; KARYOTYPE; KARYOTYPE 47,XX; MENTAL DEVELOPMENT; MOTOR DEVELOPMENT; PRESCHOOL CHILD; PRIORITY JOURNAL; X CHROMOSOME INACTIVATION; X CHROMOSOME LINKAGE; CHILD; CONGENITAL MALFORMATION; ELECTROENCEPHALOGRAPHY; INFANT; PATHOPHYSIOLOGY; RADIOGRAPHY; RETINA; SCOLIOSIS;

CHILD; CHILD, PRESCHOOL; CORPUS CALLOSUM; DEVELOPMENTAL DISABILITIES; ELECTROENCEPHALOGRAPHY; EPILEPSY; FEMALE; HUMANS; INFANT; RETINA; SCOLIOSIS;

EID: 16644380566     PISSN: 09628827     EISSN: None     Source Type: Journal    
DOI: 10.1097/00019605-200410000-00012     Document Type: Article

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