TY  - JOUR 
TI  - Diagnosis of prenantal holoprosencephalic agnatia complex
PY  - 2011
issn 0016-3813
AB  - The 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.
KW  - Prenatal diagnosis
KW  - Ciencias socio biomédicas
KW  - Medical sciences
KW  - Diagnóstico diferencial
KW  - Diagnóstico prenatal
KW  - Holoprosencefalia
UR  - http://hdl.handle.net/10906/81199
ER  -