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Childhood Apraxia of Speech (CAS) in two patients with 16p11.2 microdeletion syndrome
We report clinical findings that extend the phenotype of the ∼550 kb 16p11.2 microdeletion syndrome to include a rare, severe, and persistent pediatric speech sound disorder termed Childhood Apraxia of Speech (CAS). CAS is the speech disorder identified in a multigenerational pedigree (‘KE') in...
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| Main Authors: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Nature Publishing Group
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3598318/ https://ncbi.nlm.nih.gov/pubmed/22909774 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2012.165 |
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