Seckel Syndrome with Spontaneous Chromosomal Instability

Authors

ABDULGANİ TATAR
ZEYNEP OCAK
HAKAN DÖNERAY
ERGİN IŞIK
AHMET YEŞİLYURT
BEHZAT ÖZKAN
SITKI ÖZTAŞ

DOI

-

Abstract

Seckel syndrome is an autosomal recessive disorder characterized by prenatal and postnatal growth retardation, bird-headed face and mild mental retardation. It is a disorder involving the DNA damage-response genes. Failure in the DNA damage response and repair process can cause chromosomal instability. In addition, it is possible that there are several loci responsible for this syndrome, and variety in the molecular pathogenesis is the cause of phenotypic heterogeneity. Three different loci have been reported thus far. The effect of the locus with mutation on phenotype may be used in the subgrouping of Seckel syndrome. We report a case with Seckel syndrome having spontaneous chromosomal instability. The patient had no hematologic or malignant disease although there was a severe chromosomal instability. To date, spontaneous chromosomal instability has been reported in two cases with Seckel syndrome.

Keywords

Seckel syndrome, chromosomal instability, chromosomal breakage syndrome

First Page

77

Last Page

81

Recommended Citation

TATAR, ABDULGANİ; OCAK, ZEYNEP; DÖNERAY, HAKAN; IŞIK, ERGİN; YEŞİLYURT, AHMET; ÖZKAN, BEHZAT; and ÖZTAŞ, SITKI (2008) "Seckel Syndrome with Spontaneous Chromosomal Instability," Turkish Journal of Medical Sciences: Vol. 38: No. 1, Article 12. Available at: https://journals.tubitak.gov.tr/medical/vol38/iss1/12