01390caa a2200181   4500008004100000100001900041245007600060260000900136300000800145490002200153520079000175653008500965700001501050773006701065856004401132942001501176999001701191210629s9999    xx            000 0 und d  aAbhishek, B. P 0aAicardi Syndrome: A Case Study Highlighting Speech and Language Profile  c2019  a5-9  vVolume 5  Issue 2  aAicardi syndrome was first identified by Jean Aicardi. It is a rare genetic disorder. It is characterized by infantile spasms. Corpus Callosum Agenesis is the most prominent neurological symptom seen in this syndrome. Children affected by the syndrome are assumed to exhibit developmental delay. A 9-year-old female accompanied by her parents reported to a premiere speech and hearing institute. The client had seizures since she was 3 months old. CT of the brain revealed agenesis of corpus callosum. Speech and language evaluation revealed that the client had a massive delay in her receptive and expressive skills. Speech and language therapy was carried out for 15 sessions improvement was minimal. The minimal improvement can be attributed to the age at which therapy was started.  aCorpus Callosum, neuro-developmental, infantile spasms, scoliosis, porencephalia  aEliza Baby  aInternational Journal of Genetic Engineering and Recombination  uhttps://doi.org/10.37628/ijger.v5i2.508  cFJASyFJAS  c17844d17844