Clinical Case of Rett Syndrome: the Experience of Observing Older Preschooler
Background. Rett syndrome is a rare neuropsychiatric disorder associated with sporadic mutations in the X-linked methyl-CpG binding protein 2 (MECP2) gene. Considering the cruciality of early diagnosis, the necessity of multidisciplinary approach in the management and support of such children, the s...
Saved in:
| Main Authors: | , , |
|---|---|
| Format: | Article |
| Language: | Russian |
| Published: |
Union of pediatricians of Russia
2025-05-01
|
| Series: | Педиатрическая фармакология |
| Subjects: | |
| Online Access: | https://www.pedpharma.ru/jour/article/view/2603 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|