Noonan syndrome: prenatal diagnosis in a woman carrying a PTPN11 gene mutation
Norma Celia González-Huerta1, Juan Manuel Valdés-Miranda, Adrián Pérez-Cabrera
1Servicio de Genética, Instituto Nacional de Rehabilitación, Hospital General de México, Facultadde Medicina, Universidad Nacional Autónoma de México, México DF, México.
Objective:
To describe the case of a pregnant woman and her fetus with Noonan syndrome (NS) whom were diagnosed through ultrasonography 3D and molecular analysis of the PTPN11 gene.
Study Design:
Case report.
Conclusions:
Ultrasonography 3D is useful in the antenatal diagnosis of major congenital anomalies. Molecular studies should also be included to confirm the specific diagnosis.
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