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pro vyhledávání: '"Eulália Galhano, MD"'
Publikováno v:
Radiology Case Reports, Vol 17, Iss 12, Pp 4914-4919 (2022)
Beckwith-Wiedemann syndrome (BWS) is a rare genetic disease, characterized by macrosomia, congenital malformations and tumor predisposition, associated with genetic and epigenetic alterations in the 11p15 region. Most cases are diagnosed after birth,
Externí odkaz:
https://doaj.org/article/585f0e437e7d4fc099b278c6eac2c9d8