| Disease | hypotonia |
| Phenotype | C0004352|autism |
| Sentences | 2 |
| PubMedID- 22909152 | Consistently, the boys displayed clinical features in common with other patients carrying mecp2 duplications, including intellectual disability, autism, lack of speech, slight hypotonia and unsteadiness of movement. |
| PubMedID- 22842227 | Both children also had global developmental delay, non-verbal autism with stereotypies, hypotonia with joint hypermobility and dysmorphic facies. |
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