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First Case Report of Smith–Magenis Syndrome (SMS) Among the Arab Community in Nazareth: View and Overview

Smith–Magenis syndrome (SMS0) is a complex and rare genetic multisystem disorder characterized by a variable pattern of cognitive deficits accompanied by a1 distinctive behavioral phenotype. SMS is characterized by subtle facial dysmorphology, short stature, sleep disturbances, and neurobehavioral a...

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Detalles Bibliográficos
Autores principales: Nijim, Yousif, Adawi, Amin, Bisharat, Bishara, Bowirrat, Abdalla
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4998242/
https://www.ncbi.nlm.nih.gov/pubmed/26817868
http://dx.doi.org/10.1097/MD.0000000000002362

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