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Otocephaly

Known as: AGOTC, Agnathia-otocephaly complex 
A fatal, congenital, anatomic defect of the head characterised by a total or near total absence of the lower jaw, resulting in the union or close… 
National Institutes of Health

Related topics

Related topics

20 relations
AglossiaAgnathiaAutosomal dominant inheritanceAutosomal recessive inheritance

Broader (1)

Craniofacial Abnormalities

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2003
2003
Prenatal diagnosis of otocephaly with microphthalmia/anophthalmia using ultrasound and magnetic resonance imaging
A 30-year-old primigravid woman was referred to hospital at 29 weeks’ gestation because of polyhydramnios and regular uterine… 
Highly Cited
1998
Highly Cited
1998
Prenatal diagnosis of otocephaly using two‐dimensional and three‐dimensional ultrasonography
We report a case of the prenatal diagnosis of a very rare anomaly, namely isolated otocephaly, using two‐dimensional and three… 
1998
1998
Otocephaly: prenatal sonographic diagnosis.
Otocephaly is a rare and often lethal, nonfamilial syndrome characterized by severe mandibular hypoplasia or agnathia… 
1996
1996
Nonlethal case of otocephaly and its implications for treatment.
Otocephaly is a craniofacial syndrome with a constellation of findings consistent with symmetrically deficient development of the… 
Highly Cited
1996
Highly Cited
1996
Otx1 function overlaps with Otx2 in development of mouse forebrain and midbrain
Background: We previously reported that the homozygous mutation of Otx2 gene, a mouse cognate of the Drosophila head gap gene… 
1996
1996
Otocephalus: Histopathology and Three-Dimensional Reconstruction
1987
1987
Cyclopia-otocephaly association: a new case of the most severe variant of agnathia-holoprosencephaly complex.
This report describes a new case of true cyclopia with otocephaly and additional brain malformations (alobar holoprosencephaly… 
1984
1984
An anatomical study of human otocephaly.
This study describes the gross anatomic variations observed in a 32-week male fetus diagnosed as having otocephaly. Special… 
1982
1982
Alobar holoprosencephaly and otocephaly in a female infant with a normal karyotype and placental villitis.
The proband was born to a 24-year-old gravida 1, para 0 black woman after a 35 week gestation complicated by polyhydramnios… 
1976
1976
Prevention of caffeine-induced cleft palate by L-glutamic acid.
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