Skip to search formSkip to main contentSkip to account menu

Opitz trigonocephaly syndrome

Known as: C SYNDROME, Trigonocephaly syndrome, syndrome c 
National Institutes of Health

Related topics

Related topics

26 relations
Autosomal recessive inheritanceByzanthine arch palateCD96, EXONIC BREAKPOINTClinodactyly

Broader (2)

CraniosynostosisIntellectual Disability

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
1995
Review
1995
"C" trigonocephaly syndrome with diaphragmnatic hernia.
We report on a 6-year-old girl with C-trigonocephaly syndrome and diaphragmatic hernia. She is severely mentally retarded and… 
Review
1995
Review
1995
"C" trigonocephaly syndrome: report of a child with agenesis of the corpus callosum and tetralogy of Fallot, and review.
We report on a new case of the Opitz "C" trigonocephaly syndrome. Our patient had agenesis of the corpus callosum, an anomaly… 
1994
1994
FISH diagnosis of partial trisomy 13 and tetrasomy 13 in a patient with severe trigonocephaly (C) phenotype.
An infant girl with manifestations resembling Optiz trigonocephaly (C) syndrome who died at age 6 days was found to have a… 
1990
1990
"C" trigonocephaly syndrome: clinical variability and possibility of surgical treatment.
We report on 3 new cases of C trigonocephaly syndrome. In addition to the findings characteristic of this condition, one of the… 
1990
1990
Partial deletion of the long arm of chromosome 11 [del(11)(q23.3----qter)] with abnormal white matter.
A patient with partial deletion of the long arm of chromosome 11[del(11)(q23.3----qter)] had macrocephalic trigonocephaly, growth… 
1990
1990
C syndrome with apparently normal development.
C syndrome is an autosomal recessive craniosynostosis syndrome with characteristic cranial, facial, palate, and joint… 
1990
1990
"C" trigonocephaly syndrome: two additional cases.
1987
1987
Terminal deletion of the short arm of chromosome 3, del(3pter-p25): a recognizable syndrome.
The 3p- syndrome (terminal deletion of the short arm of chromosome 3 with breakpoint at 3p25) was found in the G-banded… 
Review
1986
Review
1986
Diagnosis of chromosome 3 duplication q23----qter, deletion p25----pter in a patient with the C (trigonocephaly) syndrome.
The cells of a deceased patient previously reported to have the C (trigonocephaly) syndrome were reinvestigated because his… 
1975
1975
The Opitz trigonocephaly syndrome. A case report.
This is the third report, to our knowledge, of a baby with Opitz trigonocephaly syndrome of multiple congenital abnormalities… 
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy (opens in a new tab), Terms of Service (opens in a new tab), and Dataset License (opens in a new tab)