Diagnosis of prenantal holoprosencephalic agnatia complex
Pachajoa, H.; Quintero, J.C.
Gaceta Medica de Mexico 147(6): 538-540
2011
ISSN/ISBN: 0016-3813 PMID: 22116186 Document Number: 653495
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.