Psychiatric Comorbidities in 1p36 Deletion Syndrome and Their Treatment—A Case Report
1p36 deletion syndrome represents the most common terminal deletion observed in humans. Major clinical findings comprise developmental delay/intellectual disability, poor or absent expressive language, congenital central muscular hypotonia, brain anomalies, brachydactyly/camptodactyly, short feet, a...
Saved in:
| Main Author: | |
|---|---|
| Format: | article |
| Language: | EN |
| Published: |
MDPI AG
2021
|
| Subjects: | |
| Online Access: | https://doaj.org/article/809d31dd2c4d41b6959c35a932164c90 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|