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pro vyhledávání: '"Niloufar Valizadeh, MD"'
Autor:
Rahim Vakili, MD, Moein Mobini, MD, Farbod Hatami, MD, Saba Vakili, MD, Niloufar Valizadeh, MD
Publikováno v:
Radiology Case Reports, Vol 17, Iss 5, Pp 1512-1520 (2022)
Meire-Gorlin syndrome (MGS) is a rare autosomal recessive disorder characterized by a triad of short stature, microtia, and absent or hypoplastic patella. We report a 5-year-old male affected with the subtype MGS1, secondary to c.c2292t mutation of O
Externí odkaz:
https://doaj.org/article/86ea45789d444f17b342da4ed0886cb6
