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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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Detalles Bibliográficos
Autor principal:	Shen, Joseph J.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Lippincott Williams & Wilkins 2015
Materias:	Original Articles
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

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