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Ítem Diagnosis of prenantal holoprosencephalic agnatia complex(2011-11-01) Cañas Dávila, Carlos AlbertoThe complex agnatia holoprosencephaly (CAH) is characterized by absence or severe hypoplasia of the mandible, abnormal position of the ears, microstomia and holoprosencephaly. A case of mother son aged 34, gravida 3, part 2, with multiplanar three-dimensional ultrasound diagnosis of holoprosencephaly and anatomical detail otocefalia, so diagnosis of CAH was made. A review of the literature and discuss the differential diagnosis.