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Two cases of Temple–Baraitser syndrome: natural history and further delineation of the clinical and radiologic phenotypes
This study reports on two individuals with Temple–Baraitser syndrome, manifesting typical hallux and pollex findings, global developmental delay, and seizures. In the five previous cases identified to date, consistent craniofacial and osseous characteristics have been observed. The children describe...
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Lippincott Williams & Wilkins
2015
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4345968/ https://www.ncbi.nlm.nih.gov/pubmed/25629734 http://dx.doi.org/10.1097/MCD.0000000000000072 |