Y cell line in a turner mosaic: a case report
نویسندگان
چکیده
Turner Syndrome is one of the most common chromosomal aneuploidy seen in humans with an incidence of about 1: 2500 newborn females. Approximately 60% patients with Turner syndrome have 45, X karyotype while others show X chromosome abnormalities like deletions of long arm or short arm, isochromosome or ring chromosome. About 6-9% cases also show presence of Y chromosome or Y derived sequences. Turner Syndrome patients with ovarian dysgenesis and Y Cellline / Y derived sequences have higher risk of developing gonadal tumors. In the present study we report on a patient with Turner Syndrome showing mosaicism with Y cell line. Our case is a 19 yrs old unmarried female who reported to Gyn OPD with primary Amenorrhoea. She was referred to our lab for cytogenetic analysis. Routine karyotype was done using standard protocol for Giemsa trypsin banding. The Cytogenetic results were confirmed by Flourescent In Situ Hybridisation (FISH) using probes for chromosomes X and Y. The patient was a Turner mosaic with karyotype 45, X in 65% and 46, XX in 10% of the cells; the remaining 25% of the cells showed presence of Ychromosome with karyotype 46, XY. The detection of Y-cell line is important in view of 10-30% higher risk of developing gonadal tumors. Prophylactic gonadectomy is recommended to patients of Turner syndrome with Ychromosome mosaicism and ovarian dysgenesis.
منابع مشابه
Turner Syndrome: A Unique Mosaic Case with 45,X/47,XX,+21/46,XX Cell Lines
We report an extremely rare case of Turner syndrome mosaicism in a 30-year-old woman. At least 100 metaphases were observed and analyzed through GTG banding with over 550 band resolutions observed. G-banded chromosome analysis revealed a mosaic female karyotype involving 3 different cell lines. One cell line (90% of the analyzed metaphases) presented monosomy X, while 6% of the cells showed tri...
متن کاملComparison of classical cytogenetics versus interphase FISH in diagnosis of mosaic form of Turner syndrome
Abstract Background: Mosaic form of turner syndrome that represented by two or more cell lines in an affected individual, often has limitation for detection with classical cytogenetic methods. The present study was carried out to compare the efficiency of interphase Fluorescence In Situ Hybridisation (FISH) and cytogenetic techniques in detection of mosaic form of turner syndrome. Method...
متن کاملSimultaneous Occurrence of Turner Syndrome and Robertsonian Translocation in a Girl with Short Stature: A Case Report
Short stature is an important clinical feature of Turner syndrome (TS). In this report, a girl with short stature suspected to have Turner syndrome underwent cytogenetic analysis, which confirmd Turner syndrome by observing sex chromosomal monosomy using the karyotype test. In addition to Turner syndrome, Robertsonian (ROB) translocation t(13;14) was detected. As recommended by a genetic counse...
متن کاملA Turner Syndrome Patient Carrying a Mosaic Distal X Chromosome Marker
A skin sample from a 17-year-old female was received for routine karyotyping with a set of clinical features including clonic seizures, cardiomyopathy, hepatic adenomas, and skeletal dysplasia. Conventional karyotyping revealed a mosaic Turner syndrome karyotype with a cell line containing a small marker of X chromosome origin. This was later confirmed on peripheral blood cultures by convention...
متن کاملAnterior segment dysgenesis in mosaic Turner syndrome.
AIMS/BACKGROUND Females with Turner syndrome commonly exhibit ophthalmological abnormalities, although there is little information in the literature documenting findings specific to Turner syndrome mosaics. Ophthalmic findings are described in four patients with mosaic Turner syndrome. All had anterior chamber abnormalities and all four had karyotypic abnormalities with a 45, X cell line. The p...
متن کامل