Silver Russel syndrome in an Aboriginal patient from Australia

Silver Russel syndrome in an Aboriginal patient from Australia

Silver-Russell syndrome (SRS OMIM 180860) is a rare, albeit well-recognized disorder characterized by severe intrauterine and postnatal growth retardation. It remains a clinical diagnosis with a molecular cause identifiable in approximately 60%–70% of patients. We report a 4-year-old Australian Abor...

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Bibliographic Details
Main Authors: Poulton, C., Azmanov, D., Atkinson, V., Beilby, J., Ewans, L., Gration, D., Dreyer, L., Shetty, V., Peake, C., McCormack, E., Palmer, Richard, Lewis, B., Dawkins, H., Broley, S., Baynam, G.
Format: Journal Article
Language:English
Published: WILEY 2018
Subjects:
Science & Technology
Life Sciences & Biomedicine
Genetics & Heredity
Aboriginal
IGF2
macrocephaly
Silver-Russel syndrome
IGF2 MUTATION
Online Access:http://hdl.handle.net/20.500.11937/83805

Internet

http://hdl.handle.net/20.500.11937/83805

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