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chorioretinal lacunae (24) 24
aicardi syndrome (18) 18
humans (15) 15
female (14) 14
infantile spasms (9) 9
agenesis of corpus callosum (8) 8
ophthalmology (8) 8
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22q11.2 deletion (1) 1
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analysis (1) 1
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Revista Brasileira de Saude Materno Infantil, ISSN 1519-3829, 10/2018, Volume 18, Issue 4, pp. 835 - 845
Abstract Introduction: the Aicardi syndrome (SA) is characterized as a rare syndrome identified in the presence of three classic characteristics: corpus... 
Infantile spasms | Aicardi' s syndrome | Agenesis of the corpus callosum | Chorioretinal lacunae | Aicardi's syndrome
Journal Article
American Journal of Medical Genetics Part C: Seminars in Medical Genetics, ISSN 1552-4868, 12/2018, Volume 178, Issue 4, pp. 423 - 431
Journal Article
世界放射学杂志:英文版(电子版), ISSN 1949-8470, 2014, Volume 6, Issue 7, pp. 511 - 514
Aicardi syndrome is a rare genetic disease characterized by a characteristic classical trio of neurological clinical abnormalities(spasms),agenesis of the... 
the | Agenesis | Transfontanellar | Aicardi | Neonate | syndrome | of | callosum | Chorioretinal | corpus | lacunae | ultrasound | Transfontanellar ultrasound | Agenesis of the corpus callosum | Aicardi syndrome | Chorioretinal lacunae | Case Report
Journal Article
Indian Journal of Human Genetics, ISSN 0971-6866, 02/2012, Volume 17, Issue 3
Aicardi syndrome is a genetic disorder characterized by the triad of infantile spasm in flexion, callosal agenesis and ocular abnormalities (chorioretinal... 
chorioretinal lacunae | coloboma | Callosal agenesis | infantile spasm
Journal Article
Journal Francais d'Ophtalmologie, ISSN 0181-5512, 12/2012, Volume 35, Issue 10, pp. 754 - 759
Introduction: Aicardi syndrome is a severe congenital disorder affecting females and characterized by a triad of symptoms, including infantile spasms, agenesis... 
Agenesis of corpus callosum | Aicardi syndrome | Chorioretinal lacunae | Mental retardation
Journal Article
JOURNAL FRANCAIS D OPHTALMOLOGIE, ISSN 0181-5512, 12/2012, Volume 35, Issue 10, pp. 754 - 759
Introduction. - Aicardi syndrome is a severe congenital disorder affecting females and characterized by a triad of symptoms, including infantile spasms,... 
OPHTHALMOLOGY | Mental retardation | CHORIORETINAL DYSPLASIA | Aicardi syndrome | Agenesis of corpus callosum | Chorioretinal lacunae
Journal Article
Journal of the Bahrain Medical Society, ISSN 1015-6321, 04/2010, Volume 22, Issue 2, pp. 76 - 78
Journal Article
02/2012
Aicardi syndrome is a genetic disorder characterized by the triad of infantile spasm in flexion, callosal agenesis and ocular abnormalities (chorioretinal... 
chorioretinal lacunae | coloboma | infantile spasm | Callosal agenesis
Web Resource
Brain and Development, ISSN 0387-7604, 2007, Volume 29, Issue 7, pp. 443 - 446
Journal Article
Archivos de la Sociedad Espanola de Oftalmologia, ISSN 0365-6691, 01/2008, Volume 83, Issue 1, pp. 29 - 36
Journal Article
Indian Journal of Human Genetics, ISSN 0971-6866, 09/2011, Volume 17, Issue 3, pp. 226 - 228
Aicardi syndrome is a genetic disorder characterized by the triad of infantile spasm in flexion, callosal agenesis and ocular abnormalities (chorioretinal... 
coloboma | chorioretinal lacunae | Callosal agenesis | infantile spasm | Case studies | Eye diseases | Care and treatment | Diagnosis | Seizures (Medicine) | Medical research | Genetic disorders | Cysts | Chromosomes | Case Report
Journal Article
American Journal of Ophthalmology Case Reports, ISSN 2451-9936, 12/2018, Volume 12, pp. 61 - 64
Purpose: To describe an unusual case of Aicardi Syndrome that both affirms hallmark characteristics of the condition and introduces new observations.... 
Posterior lens capsule | Aicardi syndrome | Corpus callosum | Chorioretinal lacunae
Journal Article
CHRISMED Journal of Health and Research, ISSN 2348-3334, 7/2018, Volume 5, Issue 3, pp. 236 - 238
Aicardi syndrome is a rare genetic disease characterized by a characteristic classical trio of neurological clinical abnormalities (spasms), agenesis of the... 
heterotopia | Aicardi | corpus callosum | chorioretinal lacunae
Journal Article
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