𝔖 Bobbio Scriptorium
✦   LIBER   ✦

PCR detection of Y-specific sequences in patients with Ullrich-Turner syndrome: Clinical implications and limitations

✍ Scribed by Osipova, G.R.; Karmanov, M.E.; Kozlova, S.I.; Evgrafov, O.V.


Publisher
John Wiley and Sons
Year
1998
Tongue
English
Weight
20 KB
Volume
76
Category
Article
ISSN
0148-7299
DOI
10.1002/(sici)1096-8628(19980401)76:4<283::aid-ajmg1>3.0.co;2-r

No coin nor oath required. For personal study only.

✦ Synopsis


Cytogenetic analysis of patients with Ullrich-Turner syndrome (UTS) may fail to detect low levels of Y chromosome mosaicism or Y-derived marker chromosomes. More sensitive polymerase chain reaction (PCR)-based tests have been developed; however, applicability of these data to prognosis of virilization and gonadoblastoma development has not been investigated adequately. We used a multiplex PCR-based method to detect two Y-specific sequences, SRY and AMGLY. Thirteen patients with UTS without cytogenetically detected Y chromosomes were studied. Y-specific sequences were detected in 5 patients by multiplex PCR. A cryptic translocation involving the Y chromosome was found in one patient with severe virilization of external genitalia and a male phenotype. Y chromosomal mosaicism was detected in peripheral blood and in both gonads of one patient, and only in the left gonad of another patient. Existence of a Y-derived marker was demonstrated in 2 patients, one of whom had no testicular tissue or virilization. Consistent with previous reports, we conclude that PCR is more sensitive than classical cytogenetic analysis and detects patients with Y-specific sequences in blood cells. However, the absence of Y-specific material in blood is not a sufficient reason to reject surgical treatment in case of virilization.


πŸ“œ SIMILAR VOLUMES


Frequency of Y chromosomal material in M
✍ LοΏ½pez, Marisol; Canto, Patricia; Aguinaga, MοΏ½nica; Torres, Leda; Cervantes, Alic πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 26 KB

Cytogenetic studies have shown that 40-60% of patients with Ullrich-Turner syndrome (UTS) are 45,X, whereas the rest have structural aberrations of the X chromosome or mosaicism with a second cell line containing a structurally normal or abnormal X or Y chromosome. However, molecular analysis has de

Relatively longer hand in patients with
✍ Uematsu, Ayumi; Yorifuji, Tohru; Muroi, Junko; Yamanaka, Chutaro; Momoi, Toru πŸ“‚ Article πŸ“… 1999 πŸ› John Wiley and Sons 🌐 English βš– 21 KB πŸ‘ 2 views

We analyzed the total hand length (HL) and length of noncarpal bones (NCL) in 50 Japanese patients with Ullrich-Turner syndrome (UTS) and in 443 other patients with short stature used as controls. In each patient group we calculated relative HL (RHL= HL/ height) and relative NCL (RNCL= NCL/ height).

Cervical ribs in fetuses with Ullrich-Tu
✍ KjΓ¦r, Inger; Hansen, Birgit Fischer πŸ“‚ Article πŸ“… 1997 πŸ› John Wiley and Sons 🌐 English βš– 14 KB πŸ‘ 2 views

The purpose of this study was to analyze the cervical skeleton in fetuses with Ullrich-Turner syndrome (45,X) in a search for skeletal characteristics in the neck region affected by hygroma. In connection with requested autopsies, 9 second trimester human fetuses were investigated radiographically b

Down syndrome: Perinatal complications a
✍ Spahis, Joanna K.; Wilson, Golder N. πŸ“‚ Article πŸ“… 1999 πŸ› John Wiley and Sons 🌐 English βš– 21 KB πŸ‘ 1 views

Two hundred and sixteen infant evaluations were selected for analysis from those of 669 outpatients (930 total visits) at a weekly Down syndrome clinic. Each record contained perinatal history and physical examination results, and 191 of the 216 included a systematic interview regarding parental exp

Cardiac malformations in patients with o
✍ Digilio, Maria Cristina; Marino, Bruno; Ammirati, Antonio; Borzaga, Umberto; Gia πŸ“‚ Article πŸ“… 1999 πŸ› John Wiley and Sons 🌐 English βš– 66 KB

## Oral -facial-skeletal (OFS) syndromes include short rib-polydactyly (SRP) and oralfacial-digital (OFD) syndromes. Congenital heart defect (CHD), mainly atrioventricular canal defect (AVCD), is a cardinal finding in the Ellis-van Creveld (EVC) syndrome, but it occurs only occasionally in other SR

Delineation of the common critical regio
✍ Wu, Yuan-Qing; Sutton, V. Reid; Nickerson, Elizabeth; Lupski, James R.; Potocki, πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 50 KB

Williams syndrome (WS) is a neurodevelopmental disorder with a variable phenotype. Molecular genetic studies have indicated that hemizygosity at the elastin locus (ELN) may account for the cardiac abnormalities seen in WS, but that mental retardation and hypercalcemia are likely caused by other gene