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...
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| Format: | article |
| Language: | EN |
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MDPI AG
2021
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| Online Access: | https://doaj.org/article/809d31dd2c4d41b6959c35a932164c90 |
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