Aicardi Syndrome Foundation Information about the disease, a medical survey, where to get help, publications and a chat room for Category Health Conditions and Diseases aicardi syndromeaicardi syndrome Foundation Logo, Welcome to the aicardi syndrome Family Website. Welcometo the aicardi syndrome website. We are glad you have found us! http://www.aicardisyndrome.org/
Extractions: Welcome What is Aicardi Syndrome? Support and Contacts Information from Parents ... Resources Welcome to the Aicardi Syndrome website. We are glad you have found us! We hope that this site can provide information and comfort to families and friends of girls diagnosed with Aicardi Syndrome. If you are here because of a newly diagnosed child, please let us know who you are. Visit our support and contacts page to sign up for our newsletter, join our email support group, and contact your regional coordinator. These resources can hopefully answer some of the questions you may have, as well as provide support. We are always open to suggestions about the site. Please email your ideas (and any technical problems) to web@aicardisyndrome.org or use our feedback form. Note: The chat room link has been moved to "support and contacts". Please send website suggestions and technical problem reports to web@aicardisyndrome.org or fill out a feedback form.
NINDS Aicardi Syndrome Information Page Information sheet compiled by National Institute of Neurological Disorders and Stroke. http://www.ninds.nih.gov/health_and_medical/disorders/aicardi.htm
Extractions: Aicardi syndrome is a rare disorder characterized by the partial or complete agenesis (absence) of the corpus callosum (the structure that links the 2 hemispheres of the brain), infantile spasms (a form of childhood seizure), mental retardation, and an ocular (eye) abnormality called lacunae (lesions) of the retina of the eye. Aicardi syndrome may be associated with other brain defects such as microcephaly (small brain) or porencephalic cysts (cerebrospinal fluid-filled cavities or gaps in the brain). Onset of Aicardi syndrome generally begins between the ages of 3 and 5 months. The disorder affects only females. Is there any treatment?
Extractions: printer friendly AICARDI SYNDROME home more about us in your area conditions information ... how you can help search this site Aicardi syndrome is a very rare neurological condition due to a congenital abnormality of brain development. The characteristic features consist of under development or absence of the development (agenesis) of a brain structure known as the corpus callosum, a form of epilepsy (infantile spasms) and an abnormality to the structure and appearance of the retina of the eyes. It is an example of one of the syndromic causes of agenesisof the corpus callosum . In Aicardi syndrome, in addition to the structural abnormality of the corpus callosum, other structures within the brain can also be abnormal. This can result in a variety of types of brain cyst and/or abnormal structure within areas of both grey or white matter of the brain. Learning Disability is a constant feature and varies from moderate to the more commonly seen severe picture. The associated epilepsy classically takes the form of "infantile spasms" or is "spasm-like". Other types of epileptic fit may be seen. The epilepsy usually occurs by two months of age, it is often difficult and remains difficult to control. Investigating it with electroencephalogramstudies may reveal a pattern characteristic of these spasms (hypsarrhythmia). This form of epilepsy is sometimes referred to as
AICARDI SYNDROME Pediatric Database (PEDBASE); Discipline GEN; Last Updated 6/12/94 AICARDISYNDROME. DEFINITION INTERNET LINKS aicardi syndrome Foundation. http://www.icondata.com/health/pedbase/files/AICARDIS.HTM
Aicardi Syndrome A list of synonyms of aicardi syndrome, a summary and the major features. http://www.nlm.nih.gov/mesh/jablonski/syndromes/syndrome015.html
Extractions: Syndrome Aicardi syndrome Synonyms chorioretinal anomalies-corpus callosum agenesis-infantile spasms syndrome corpus callosum agenesis-chorioretinal abnormality syndrome corpus callosum agenesis-chorioretinopathy-infantile spasms syndrome corpus callosum agenesis-ocular anomalies-salaam seizures syndrome Summary A syndrome of infantile spasms, typical bowing of the head (salaam seizures), chorioretinopathy, retarded mental and motor development, agenesis of the corpus callosum, and costovertebral anomalies. Major Features Head and neck: Skull abnormalities include frontal bossing, occipital flattening, and plagiocephaly. Eyes: Chorioretinal lacunae and, less frequently, unilateral microphthalmia, eyelid twitching, optic nerve coloboma, nystagmus, and retinal detachment. Mouth and oral structures: Occasional cleft lip and palate. Thorax: Absent or abnormal ribs. Extremities: Unilateral hip dysplasia may occur. Spine: Vertebral abnormalities include hemivertebrae and scoliosis. Muscles: Hypotonia.
MEDLINEplus Medical Encyclopedia: Aicardi Syndrome aicardi syndrome a list of alternate names, a definition with a look at the causes, incidence and risk factors. http://www.nlm.nih.gov/medlineplus/ency/article/001664.htm
Extractions: Skip navigation Other encyclopedia topics: A-Ag Ah-Ap Aq-Az B-Bk ... Z Contents of this page: Corpus callosum of the brain Definition Return to top Aicardi syndrome is a rare genetic disorder characterized by infantile spasms (jerking), absence of the corpus callosum (the connection between the two hemispheres of the brain), mental retardation, and lesions of the retina of the eye or optic nerve. Causes, incidence, and risk factors Return to top The cause of Aicardi syndrome is unknown at this time, but is presumed to be a genetic disorder carried on the X-chromosome in some cases and a random, sporadic mutation in others. There are less than 500 cases of Aicardi worldwide. Symptoms Return to top Children are most commonly diagnosed with Aicardi Syndrome between the ages of three months and five months, if they meet the following criteria: Female sex (or XXY genotype male) Retinal lacunae lesions of the retina Seizures typically beginning as infantile spasms, a type of epileptic disorder in infants
Extractions: (advertisement) Home Specialties CME PDA ... Patient Education Articles Images CME Patient Education Advanced Search Link to this site Back to: eMedicine Specialties Pediatrics Genetics And Metabolic Disease Last Updated: January 7, 2002 Rate this Article Email to a Colleague Synonyms and related keywords: callosal agenesis, ocular abnormalities, syndrome of spasm-in-flexion AUTHOR INFORMATION Section 1 of 11 Author Information Introduction Clinical Differentials ... Bibliography Author: Marc P Difazio, MD , Chief, Child and Adolescent Neurology Clinic, Assistant Professor, Department of Neurology, Section of Child and Adolescent Neurology, Walter Reed Army Medical Center Coauthor(s): Ronald G Davis, MD , Assistant Professor, Department of Neurology, Division of Child and Adolescent Neurology, Children's Hospital of Boston and Harvard University Medical School Marc P Difazio, MD, is a member of the following medical societies: Alpha Omega Alpha , American Academy of Neurology, and Child Neurology Society Editor(s): James Bowman, MD
Aicardi Syndrome Foundation aicardi syndrome Foundation Logo, aicardi syndrome. By the aicardi syndromeNewsletter, A publication of the aicardi syndrome Foundation, Inc. http://www.aicardisyndrome.org/index.php?pname=whatis
NINDS - News And Events Health. Sorry! There are no press releases for aicardi syndrome. Useyour browser's Back button to return to your previous activity. http://www.ninds.nih.gov/health_and_medical/news.htm?url=/health_and_medical/dis
Agenesis Of The Corpus Callosum/Aicardi Syndrome -CORPAL A support group for the families and carers of those with Agenesis of the Corpus Callosum, and aicardi syndrome. Information, reports and newsletters. http://freespace.virgin.net/jan.webster/index.htm
Extractions: By Janet Webster Animated Gifs by and Although great care has been taken in the compilation and preparation of the enclosed details to ensure accuracy, CORPAL cannot accept responsibility for any errors or omissions. Any medical information provided is for information/education purposes, you should obtain further information from your medical practitioner. HI
Aicardi Syndrome Related Search Search for books about aicardi syndrome. aicardi syndrome. Begin your search for. aicardi syndrome http://www.book-summary.com/aicardi-syndrome.html
Congenital, Hereditary, And Neonatal Diseases And Abnormalities Comprehensive list of links from Karolinska Institutet, Sweden.Category Health Nursing Specialties Neonatal aicardi syndrome (not on MeSH) aicardi syndrome Foundation (US);aicardi syndrome information - NINDS/NIH (US); aicardi syndrome http://www.mic.ki.se/Diseases/c16.html
Aicardi Syndrome / The Family Village Library Library A B. aicardi syndrome. Who to Contact. Al and Cindy Meo AicardiSyndrome Foundation PO Box 3202 St. Charles, IL 60174 (800 http://www.familyvillage.wisc.edu/lib_aica.htm
Extractions: E-mail: AICNews@aol.com The Aicardi Syndrome Newsletter provides information and support to families who have a child with Aicardi syndrome and acts as an information gathering and sharing resource for professional and health care personnel. The Newsletter provides a network of information, communication and support to families, strengthens and empowers families in becoming advocates for their child, and gathers current research articles and findings regarding Aicardi syndrome and other related topics for distribution to member families. Aicardisyndrome
Aicardi Syndrome Foundation aicardi syndrome AN INFORMATION NETWORK FOR FAMILIES AND PROFESSIONALS By the AicardiSyndrome Newsletter, A publication of the aicardi syndrome Foundation, Inc http://www.aicardi.com/Aicardi.htm
Aicardi Syndrome Foundation aicardi syndrome Foundation* New Address to be given soon. USA. Phone1800-374-8518. Denise Parsons aicardi syndrome Newsletter, Inc. http://www.aicardi.com/info.htm
Aicardi Syndrome aicardi syndrome is a rare disorder characterized by the agenesis of the corpuscallosum, infantile spasms, mental retardation, and lacunae of the retina. http://healthlink.mcw.edu/article/921381662.html
Extractions: Subscribe now >> Aicardi syndrome is a rare disorder characterized by the partial or complete agenesis (absence) of the corpus callosum (the structure that links the 2 hemispheres of the brain), infantile spasms (a form of childhood seizure), mental retardation, and an ocular (eye) abnormality called lacunae (lesions) of the retina of the eye. Aicardi syndrome may be associated with other brain defects such as microcephaly (small brain) or porencephalic cysts (cerebrospinal fluid-filled cavities or gaps in the brain). Onset of Aicardi syndrome generally begins between the ages of 3 and 5 months. The disorder affects only females. There is no cure for Aicardi syndrome nor is there a standard course of treatment. Treatment, which is symptomatic, generally involves management of seizures and intervention programs for mental retardation. What is the prognosis?
Aicardi Syndrome aicardi syndrome. aicardi syndrome Newsletter, Inc. 5115 Troy 6033. AicardiSyndrome Awareness and Support Group 29 Delavan Ave. Toronto http://www.kumc.edu/gec/support/aicardi.html
Aicardi Syndrome - Keep Kids Healthy Conditions Main Diseases and Conditions aicardi syndrome. aicardi syndrome. Aicardisyndrome abnormalities. Resource List for aicardi syndrome Aicardi http://www.keepkidshealthy.com/welcome/conditions/aicardi.html
Extractions: Main Diseases and Conditions Aicardi syndrome is a rare disorder that affects females, and whose features include partial or compete agenesis of the corpus collosum (the structure that connects to the two halves of the brain), seizures that are difficult to control with antiseizure medications, mental retardation and abnormalities of the retina in the eye (especially colobomas The kind of seizures that infants with Aicardi syndrome usually have are infantile spasms . These seizures consist of symmetric and brief clusters of spasms of the muscles of the neck, trunk or limbs. An EEG can help to diagnose if your child is having infantile spasms, because it will show a very characteristic, abnormal pattern called hypsarrhythmia. Treatment of infantile spasms can be very difficult and your child may require treatment with many different types of medications, including clonazepam, valproate, pyridoxine, and hormonal therapy with adrenocorticotropic hormone (ACTH) or corticosteroids. Agenesis of the corpus collosum can occur by itself, without seizures, mental retardation or other medical problems. These children will usually be normal without other brain or developmental abnormalities.
Aicardi Syndrome aicardi syndrome. I am looking for patients with aicardi syndrome forgenetic analysis. If any of you have female patients with this http://www.waisman.wisc.edu/child-neuro/seekpt-f/aicardi.html
NINDS Aicardi Syndrome Information Page More about NINDS aicardi syndrome Information Page. Content for thispage. NINDS aicardi syndrome Information Page. Reviewed 0701-2001. http://accessible.ninds.nih.gov/health_and_medical/disorders/aicardi.htm
Extractions: Disorders - National Institute of Neurological Disorders and Stroke (NINDS) Skip menus Home About NINDS Disorders-you are in this section ... Find People The nation's leading supporter of biomedical research on disorders of the brain and nervous system. Select Topic Disorder Quick Links Alzheimer's Autism Cerebral Palsy Chronic Pain Epilepsy Headache Multiple Sclerosis Parkinson's Stroke Traumatic Brain Injury Studies with patients Research literature Press release NINDS Search (search help) Contact us My privacy NINDS is part of the National Institutes of Health Contact us NINDS Aicardi Syndrome Information Page Aicardi syndrome is a rare disorder characterized by the partial or complete agenesis (absence) of the corpus callosum (the structure that links the 2 hemispheres of the brain), infantile spasms (a form of childhood seizure), mental retardation, and an ocular (eye) abnormality called lacunae (lesions) of the retina of the eye. Aicardi syndrome may be associated with other brain defects such as microcephaly (small brain) or porencephalic cysts (cerebrospinal fluid-filled cavities or gaps in the brain). Onset of Aicardi syndrome generally begins between the ages of 3 and 5 months. The disorder affects only females.