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Severe myelinopathy in 49,XXXXY syndrome

49,XXXXY is a rare aneuploidy with neuroanatomic findings scarcely reported in the literature. Given the fact that many of its phenotypic characteristics are similar to Klinefelter patients, 49,XXXXY has been treated as a variant of Klinefelter syndrome in the past. Newer studies have shown that int...

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Bibliografiska uppgifter
I publikationen:Neuroradiol J
Huvudupphovsmän: Buller, Mark A, Pfeifer, Cory M
Materialtyp: Artigo
Språk:Inglês
Publicerad: SAGE Publications 2017
Ämnen:
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC6136133/
https://ncbi.nlm.nih.gov/pubmed/28627968
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/1971400917703989
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