« Que moi » (notice n° 1595522)
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| 000 -LEADER | |
|---|---|
| fixed length control field | 02069cam a2200265 4500500 |
| 005 - DATE AND TIME OF LATEST TRANSACTION | |
| control field | 20251228073623.0 |
| 041 ## - LANGUAGE CODE | |
| Language code of text/sound track or separate title | fre |
| 042 ## - AUTHENTICATION CODE | |
| Authentication code | dc |
| 100 10 - MAIN ENTRY--PERSONAL NAME | |
| Personal name | Bourjot, Aline |
| Relator term | author |
| 245 00 - TITLE STATEMENT | |
| Title | « Que moi » |
| 260 ## - PUBLICATION, DISTRIBUTION, ETC. | |
| Date of publication, distribution, etc. | 2017.<br/> |
| 500 ## - GENERAL NOTE | |
| General note | 12 |
| 520 ## - SUMMARY, ETC. | |
| Summary, etc. | Amélie, jeune adolescente rencontrée lors d’une présentation clinique, perçoit douloureusement sa différence, sa mise à l’écart de sa famille sans pouvoir l’élaborer. Elle est restée dans une identification à sa mère telle une toute petite fille et évacue de son discours la rivalité fraternelle tout en l’agissant avec les plus jeunes qu’elle dans l’institution qu’elle fréquente. La question d’une construction du sujet selon une structure psychotique se pose du fait de la déficience de la fonction symbolique perceptible dans son discours, même si Amélie est aussi porteuse d’un handicap lié à une anomalie chromosomique. |
| 520 ## - SUMMARY, ETC. | |
| Summary, etc. | Amélie, a young teenager we met during a clinical presentation, shows evidence of a deficient symbolic function. Though painfully aware that she is kept on the sidelines by her family, she cannot elaborate her difference. She remains caught in the process of identification with her mother as a little girl and rejects all ideas of sibling rivalry while reenacting it with the younger ones in the institution she attends. In spite of her being also handicapped by a chromosomal abnormality, the question remains whether, due to a hole in the symbolic order, she has a psychotic structure or not. |
| 690 ## - LOCAL SUBJECT ADDED ENTRY--TOPICAL TERM (OCLC, RLIN) | |
| Topical term or geographic name as entry element | anomalie génétique |
| 690 ## - LOCAL SUBJECT ADDED ENTRY--TOPICAL TERM (OCLC, RLIN) | |
| Topical term or geographic name as entry element | Déficit de la fonction symbolique |
| 690 ## - LOCAL SUBJECT ADDED ENTRY--TOPICAL TERM (OCLC, RLIN) | |
| Topical term or geographic name as entry element | identification à la mère |
| 690 ## - LOCAL SUBJECT ADDED ENTRY--TOPICAL TERM (OCLC, RLIN) | |
| Topical term or geographic name as entry element | structure psychotique |
| 690 ## - LOCAL SUBJECT ADDED ENTRY--TOPICAL TERM (OCLC, RLIN) | |
| Topical term or geographic name as entry element | chromosomal abnormality |
| 690 ## - LOCAL SUBJECT ADDED ENTRY--TOPICAL TERM (OCLC, RLIN) | |
| Topical term or geographic name as entry element | Deficient symbolic function |
| 690 ## - LOCAL SUBJECT ADDED ENTRY--TOPICAL TERM (OCLC, RLIN) | |
| Topical term or geographic name as entry element | identification with the mother |
| 690 ## - LOCAL SUBJECT ADDED ENTRY--TOPICAL TERM (OCLC, RLIN) | |
| Topical term or geographic name as entry element | psychotic structure |
| 786 0# - DATA SOURCE ENTRY | |
| Note | Savoirs et clinique | 22 | 1 | 2017-02-28 | p. 115-118 | 1634-3298 |
| 856 41 - ELECTRONIC LOCATION AND ACCESS | |
| Uniform Resource Identifier | <a href="https://shs.cairn.info/revue-savoirs-et-cliniques-2017-1-page-115?lang=fr&redirect-ssocas=7080">https://shs.cairn.info/revue-savoirs-et-cliniques-2017-1-page-115?lang=fr&redirect-ssocas=7080</a> |
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