AB046. Russell-Silver syndrome: a case report and brief review of the literature

BACKGROUND: Russell-Silver syndrome (RSS) is a rare genetic disease classified as an imprinting disorder. It is characterized by intrauterine growth retardation, body asymmetry dysmorphic facie including triangular face and clinodactyly of 5th digits, and increased risk of development delay. RSS is...

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Publicat a:Ann Transl Med
Autors principals: Fernandez-Ibanez, Ana, Ugalde-Herra, Rodrigo, Carneiro-Martinez, Carolina, Verdejo-Rodriguez, Lara, Anon-Alvarez, Elena
Format: Artigo
Idioma:Inglês
Publicat: AME Publishing Company 2017
Matèries:
Birth Defects, Dysmorphology, Skeletal Dysplasia, Craniofacial Anomalies
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC5641707/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.21037/atm.2017.s046
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