Case Reports
Trigonocephaly and the 11q- syndrome
- PMID: 302679
Item in Clipboard
Case Reports
Trigonocephaly and the 11q- syndrome
Ann Genet.
1977 Mar.
Abstract
A seventh case of deletion of the distal long arm of a chromosome 11 is described. As in other cases with this karyotypic abnormality, trigonocephaly is the most noticeable phenotypic peculiarity. A review of common developmental and dysmorphic features among the seven recognized cases is presented.
Similar articles
-
Deletion of 11q: report of two cases and a review.Birth Defects Orig Artic Ser. 1976;12(5):125-30. Birth Defects Orig Artic Ser. 1976. PMID: 953212
-
[Partial monosomy 11q. A new case].Ann Genet. 1977 Mar;20(1):63-6. Ann Genet. 1977. PMID: 302678 French.
-
Chromosome 11 long arm partial deletion: a new syndrome.Am J Ment Defic. 1976 Jan;80(4):473-5. Am J Ment Defic. 1976. PMID: 1247044
-
Opitz-C syndrome: on the nosology of mental retardation and trigonocephaly.Genet Couns. 1992;3(4):209-15. Genet Couns. 1992. PMID: 1472356 Review.
-
Distal deletion of the long arm of chromosome number 1 (q43-->qter) associated with severe mental retardation and a nonspecific dysmorphic syndrome.Ann Genet. 1992;35(3):167-9. Ann Genet. 1992. PMID: 1466567 Review.
Cited by
-
Partial monosomy 10p syndrome.Eur J Pediatr. 1981 Oct;137(2):243-6. doi: 10.1007/BF00441326. Eur J Pediatr. 1981. PMID: 7308236
-
Partial deletion of the long arm of chromosome 11 the Jacobsen syndrome.Indian J Pediatr. 1984 May-Jun;51(410):359-62. doi: 10.1007/BF02754688. Indian J Pediatr. 1984. PMID: 6511057 No abstract available.
-
Partial deletion of the long arm chromosome 11 in Jacobsen syndrome.Indian J Pediatr. 1986 Jan-Feb;53(1):123-6. doi: 10.1007/BF02787084. Indian J Pediatr. 1986. PMID: 3759192 No abstract available.
-
Jacobsen syndrome: report of a patient with severe eye anomalies, growth hormone deficiency, and hypothyroidism associated with deletion 11 (q23q25) and review of 52 cases.J Med Genet. 1996 Sep;33(9):772-8. doi: 10.1136/jmg.33.9.772. J Med Genet. 1996. PMID: 8880580 Free PMC article. Review.
-
Craniosynostosis and syndactyly: expanding the 11q-- chromosomal deletion phenotype.J Med Genet. 1980 Dec;17(6):480-3. doi: 10.1136/jmg.17.6.480. J Med Genet. 1980. PMID: 7205433 Free PMC article.
Publication types
MeSH terms
LinkOut - more resources
Research Materials