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First-Trimester Diagnosis of Agnathia-Otocephaly Complex: A Series of 4 Cases and Review of the Literature.
Rodriguez N, Casasbuenas A, Andreeva E, Odegova N, Wong AE, Sepulveda W. Rodriguez N, et al. J Ultrasound Med. 2019 Mar;38(3):805-809. doi: 10.1002/jum.14759. Epub 2018 Aug 31. J Ultrasound Med. 2019. PMID: 30171631 Review.
First-trimester ultrasound findings in 4 fetuses with agnathia-otocephaly complex are described. In addition, information from 3 cases reported in the literature was also reviewed, for a total of 7 cases analyzed. ...This report highlights the important role …
First-trimester ultrasound findings in 4 fetuses with agnathia-otocephaly complex are described. In addition, informati …
Isolated Agnathia-Otocephaly Complex Diagnosed Prenatally for Ex-Utero Intrapartum Treatment: A Case Report.
Suemitsu T, Takesawa A, Hosokawa M, Mitani T, Kadooka M, Furusawa Y, Kawataki M, Dohi S. Suemitsu T, et al. Am J Case Rep. 2023 May 11;24:e939016. doi: 10.12659/AJCR.939016. Am J Case Rep. 2023. PMID: 37165610 Free PMC article.
BACKGROUND Agnathia-otocephaly complex (AOC) is a rare congenital malformation due to a first-branch arch disorder and has been considered lethal. ...
BACKGROUND Agnathia-otocephaly complex (AOC) is a rare congenital malformation due to a first-branch arch disorder and …
Severe Agnathia-Otocephaly Complex: Surgical Management and Longitudinal Follow-up From Birth Through Adulthood.
Golinko MS, Shetye P, Flores RL, Staffenberg DA. Golinko MS, et al. J Craniofac Surg. 2015 Nov;26(8):2387-92. doi: 10.1097/SCS.0000000000002150. J Craniofac Surg. 2015. PMID: 26517463
Agnathia-otocephaly complex (AOC) is characterized by mandibular hypo- or aplasia, ear abnormalities, microstomia, and microglossia. ...
Agnathia-otocephaly complex (AOC) is characterized by mandibular hypo- or aplasia, ear abnormalities, microstomia, and …
Prenatal ultrasound findings of holoprosencephaly spectrum: Unusual associations.
El-Dessouky SH, Aboulghar MM, Gaafar HM, Abdella RM, Sharaf MF, Ateya MI, Elarab AE, Zidan WH, Helal RM, Aboelsaud SM, Eid MM, Abdel-Salam GMH. El-Dessouky SH, et al. Prenat Diagn. 2020 Apr;40(5):565-576. doi: 10.1002/pd.5649. Epub 2020 Feb 10. Prenat Diagn. 2020. PMID: 31955448
Interestingly, among them, four cases (16%) presented with the rare agnathia-otocephaly complex. Chromosomal abnormalities were detected in 11 cases (44%), the most frequent being trisomy 13 in seven cases (five alobar, one semilobar, and one lobar HPE), foll …
Interestingly, among them, four cases (16%) presented with the rare agnathia-otocephaly complex. Chromosomal abnormalit …