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Cebocephaly

Known as: cebocephalus 
A congenital abnormality characterized by a malformation of the head. The eyes are hypoteleric and the nose may be absent or misshapen (small… 
National Institutes of Health

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3 relations
Clinical Data Interchange Standards Consortium TerminologyCongenital AbnormalityCyclocephaly

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2011
2011
Rapid aneuploidy diagnosis by multiplex ligation-dependent probe amplification and array comparative genomic hybridization in pregnancy with major congenital malformations.
2003
2003
Alobar holoprosencephaly: report of two cases with unusual findings.
Holoprosencephaly, a disorder resulting from failure of cleavage or incomplete differentiation of the forebrain structures at… 
Review
1997
Review
1997
Prenatal diagnosis of de novo proximal interstitial deletion of 14q associated with cebocephaly.
We report on the prenatal diagnosis of a case of cebocephaly, alobar holoprosencephaly, and microcephaly associated with a de… 
1990
1990
An anatomic comparison of cebocephaly and ethmocephaly.
Cebocephaly (hypotelorism, single-nostril nose) and ethmocephaly (hypotelorism, interorbital proboscis) lie in the middle of the… 
1984
1984
Cyclopia and cebocephaly in two newborn infants with unbalanced segregation of a familial translocation rcp (1;7)(q32;q34).
This is a report of a family with a balanced reciprocal translocation, rcp (1;7)(q32;q34). Among pregnancies from translocation… 
1977
1977
Ocular findings in triploidy.
1977
1977
Cebocephaly in an infant with trisomy 18.
An infant who died in the perinatal period with the unusual association of trisomy 18 and cebocephaly is described. It is… 
1970
1970
Familial Cebocephaly
bral anomalies form a spectrum of disorders. At one end of the spectrum is cyclopia with a single or partly divided eye in a… 
1968
1968
Short arm deletion of chromosome 18 in cebocephaly.
THE holoprosencephalies form a spectrum of graded teratologic entities with cyclopia as the most extreme example. As a group… 
1968
1968
Arrhinencephaly associated with a deficiency involving chromosome 18.
Bilateral harelip, cleft palate, and some form of arrhinencephalic malformation of the brain are among the more common striking… 
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