We report on a girl who, despite her 45,X/46,X,der(Y) karyotype, showed no signs of virilization or physical signs of the Ullrich-Turner syndrome (UTS), except for a reduced growth rate. After prophylactic gonadectomy due to the risk of developing gonadoblastoma, the gonads and peripheral blood samples were analyzed by fluorescence in situ hybridization (FISH) and polymerase chain reaction (PCR) to detect Y-specific sequences. These analyses allowed Lis to characterize the Y-derived chromosome as being an isodicentric Yp chromosorne (idic(Yp)) and showed a pronounced difference in the distribution of the 45,X/46,X,idic(Yp) mosaicism between the two analyzed tissues. It was shown that, although in peripheral blood almost all cells (97.5%) be...
AbstractIntroductionWe present a rare patient case with mixed gonadal dysgenesis as a disorder of se...
A 45,X karyotype is one of the common chromosomal abnormalities characterized by short stature, lack...
Turner syndrome is one of the most common chromosomal abnormalities affecting newborn females. More ...
We report here on a girl who, despite her 45,X/46,X,der(Y) karyotype, showed no signs of virilizatio...
We describe a woman with Ullrich-Turner manifestations and a 45,X/46,X,+mar karyotype. Fluorescence ...
Karyotype investigations using classical cyto-genetics, fluorescence in situ hybridization (FISH) an...
of 45,X/46,Xidic(Y) mosaicism and therapeutic implications: case report Hospital de São João, Faculd...
We describe a woman with Ullrich-Turner manifestations and a 45,X/46, X,+mar karyotype. Fluorescence...
CONTEXT: 45,X/46,Xidic(Y) mosaicism demands careful and thorough study because of both its variable ...
Objective: To determine the clinical implications of the presence of a Y chromosome in Turner's synd...
The presence of Y chromosome fragments in patients with Turner's syndrome (TS) is known to increase ...
Introduction: We present a rare patient case with mixed gonadal dysgenesis as a disorder of sex deve...
Objective: The gene SRY[sex determining region of the Y] located at the distal region of the short a...
Background: The potential involvement of SRY in abnormal gonadal development in 45,X/46,X,der(Y) pat...
A two-year-and-eight-month-old girl presented with clitoromegaly and short stature. Two cell lines, ...
AbstractIntroductionWe present a rare patient case with mixed gonadal dysgenesis as a disorder of se...
A 45,X karyotype is one of the common chromosomal abnormalities characterized by short stature, lack...
Turner syndrome is one of the most common chromosomal abnormalities affecting newborn females. More ...
We report here on a girl who, despite her 45,X/46,X,der(Y) karyotype, showed no signs of virilizatio...
We describe a woman with Ullrich-Turner manifestations and a 45,X/46,X,+mar karyotype. Fluorescence ...
Karyotype investigations using classical cyto-genetics, fluorescence in situ hybridization (FISH) an...
of 45,X/46,Xidic(Y) mosaicism and therapeutic implications: case report Hospital de São João, Faculd...
We describe a woman with Ullrich-Turner manifestations and a 45,X/46, X,+mar karyotype. Fluorescence...
CONTEXT: 45,X/46,Xidic(Y) mosaicism demands careful and thorough study because of both its variable ...
Objective: To determine the clinical implications of the presence of a Y chromosome in Turner's synd...
The presence of Y chromosome fragments in patients with Turner's syndrome (TS) is known to increase ...
Introduction: We present a rare patient case with mixed gonadal dysgenesis as a disorder of sex deve...
Objective: The gene SRY[sex determining region of the Y] located at the distal region of the short a...
Background: The potential involvement of SRY in abnormal gonadal development in 45,X/46,X,der(Y) pat...
A two-year-and-eight-month-old girl presented with clitoromegaly and short stature. Two cell lines, ...
AbstractIntroductionWe present a rare patient case with mixed gonadal dysgenesis as a disorder of se...
A 45,X karyotype is one of the common chromosomal abnormalities characterized by short stature, lack...
Turner syndrome is one of the most common chromosomal abnormalities affecting newborn females. More ...