[Human isodicentric X-chromosomes]
- PMID: 601863
[Human isodicentric X-chromosomes]
Abstract
The large submetacentric abnormal late replicating X-chromosomes were found in three patients under karyological studies of 168 patients with Turner's syndrome. G- and C-banding revealed that abnormal chromosomes are three variants of isodicentric chromosomes resulting from the junction of the short arms of two X-chromosomes. The patients' karyotypes are respectively: 45,X/46,X,dic (X)(qter leads to p22: :p22 leads to qter); 46X,dic(X)(qter leads to p21: :p21 leads to qter); 46,X/46,X,dic(X)(qter leads to p11: :p11 leads to qter). All the three patients had different size deficiencies of the short arm of the X-chromosome. Partial X-monosomy caused the appearance of features of the Turner syndrome, which was less expressed in our patients compared to those with the entire X-monosomy.
Similar articles
-
[Telomeric fusion of the short arms of both X chromosomes in a patient presenting an atypical Turner syndrome].J Genet Hum. 1980 Dec;28(4):131-40. J Genet Hum. 1980. PMID: 7205197 French.
-
Replication patterns of three isodicentric X chromosomes and an X isochromosome in human lymphocytes.Am J Med Genet. 1978;1(4):445-60. doi: 10.1002/ajmg.1320010407. Am J Med Genet. 1978. PMID: 665728
-
Cytogenetic findings in 125 patients with Turner's syndrome and abnormal karyotypes.J Genet Hum. 1977 Jun;25(2):95-107. J Genet Hum. 1977. PMID: 915489
-
Mental retardation and Ullrich-Turner syndrome in cases with 45,X/46X,+mar: additional support for the loss of the X-inactivation center hypothesis.Am J Med Genet. 1994 Aug 15;52(2):136-45. doi: 10.1002/ajmg.1320520204. Am J Med Genet. 1994. PMID: 7801998 Review.
-
Turner syndrome: the case of the missing sex chromosome.Trends Genet. 1993 Mar;9(3):90-3. doi: 10.1016/0168-9525(93)90230-f. Trends Genet. 1993. PMID: 8488568 Review.
Cited by
-
Further dicentric X isochromosomes and deletions, and a new structure i(X)(pter to q2102 to pter).J Med Genet. 1979 Aug;16(4):278-84. doi: 10.1136/jmg.16.4.278. J Med Genet. 1979. PMID: 490580 Free PMC article.