Aicardi Syndrome: A Case Study Highlighting Speech and Language Profile (Record no. 17844)
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| 000 -LEADER | |
|---|---|
| fixed length control field | 01390caa a2200181 4500 |
| 100 ## - MAIN ENTRY--PERSONAL NAME | |
| Personal name | Abhishek, B. P |
| 245 #0 - TITLE STATEMENT | |
| Title | Aicardi Syndrome: A Case Study Highlighting Speech and Language Profile |
| 260 ## - PUBLICATION, DISTRIBUTION, ETC. | |
| Date of publication, distribution, etc. | 2019 |
| 300 ## - PHYSICAL DESCRIPTION | |
| Extent | 5-9 |
| 490 ## - SERIES STATEMENT | |
| Volume/sequential designation | Volume 5 Issue 2 |
| 520 ## - SUMMARY, ETC. | |
| Summary, etc. | Aicardi 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. |
| 653 ## - INDEX TERM--UNCONTROLLED | |
| Uncontrolled term | Corpus Callosum, neuro-developmental, infantile spasms, scoliosis, porencephalia |
| 700 ## - ADDED ENTRY--PERSONAL NAME | |
| Personal name | Eliza Baby |
| 773 ## - HOST ITEM ENTRY | |
| Main entry heading | International Journal of Genetic Engineering and Recombination |
| 856 ## - ELECTRONIC LOCATION AND ACCESS | |
| Uniform Resource Identifier | https://doi.org/10.37628/ijger.v5i2.508 |
| 942 ## - ADDED ENTRY ELEMENTS (KOHA) | |
| Koha item type | Faculty Publications |
| -- | FJAS |
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