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         Aicardi Syndrome:     more detail
  1. Aicardi Syndrome - A Medical Dictionary, Bibliography, and Annotated Research Guide to Internet References by ICON Health Publications, 2004-08-23
  2. The Official Parent's Sourcebook on Aicardi Syndrome: A Directory for the Internet Age by Icon Health Publications, 2003-11
  3. Aicardi syndrome: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Paul Johnson, 2005

101. Bienvenue Sur Aicardi.info - A.A.L. Syndrome D'Aicardi : The Disease
information sur le syndrome d aicardi,échanges et soutien entre parents.
http://webperso.easyconnect.fr/o.vauchelet/aicardi/aicardisyndrome/thedisease.ph
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A icardi Syndrome is a rare genetic disease witch was identified in 1965 by the Pr. Jean Aicardi. I t is X-linked and therefor is only found in girls. A icardi Syndrome can be characterized by :
  • Seizures, Brain malformation (corpus callosum agenesis) Ocular anomalies
T hese combination can result in severe handicap.
S ome girls are able to walk.Language rarely present but this does not exclude all other forms of communication. A icardi Syndrome could be detected within the first months of life.

102. Aicardi S Syndrome
Complete online version of The Encyclopaedia of Medical Imaging including text and images from The Encyclopaedia of Medical Imaging s eight book volumes
http://www.amershamhealth.com/medcyclopaedia/medical/Volume VI 1/AICARDIS SYNDRO

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our commitment our company Search Medcyclopaedia for: Search marked text (mark text before you click) Browse entry words starting with: A B C D ... amershamhealth.com Aicardi's syndrome, (J Aicardi, 20th century, French neurologist), X-linked dominant disorder consisting of infantile spasms, callosal agenesis or hypogenesis, chorioretinopathy, and an abnormal EEG. The syndrome occurs almost exclusively in females with no family history of ophthalmological or neurological disease. Affected patients must have two X chromosomes, so that patients with Kleinfelter's syndrome (47 XXY) can also have it. Intracranial anomalies include callosal hypogenesis ( Fig.1 ) (typically associated with interhemispheric cysts), grey matter heterotopia cortical dysplasia , posterior fossa cysts, cerebellar hypoplasia, choroid plexus papillomas , and microphthalmia. Ophthalmologic examination reveals characteristic chorioretinal lacunae, resulting from retinal dysplasia, and ocular colobomata. Myelination may be delayed. MR examination clearly demonstrates all these features.

103. Aicardi's Syndrome With Interhemispheric Arachnoid Cyst And Sacro - Coccygeal Te
Neurol India is an peerreviewed biomedical periodical of Neurological Society of India.
http://www.neurologyindia.com/article.asp?issn=0028-3886;year=1993;volume=41;iss

104. Search The Web

http://www.aicardi.com/

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