Turner syndrome (TS) is one of the most common chromosomal abnormalities, occurring in about 50 per 100,000 female live births characterized by the total or partial loss of one X-chromosome in all or some cells. Frequently observed manifestations of TS include short stature, lymphedema, cardiac abnormalities, gonadal dysgenesis, dysmorphic features, ear and hearing problems, and a variety of other problems. Conductive hearing loss (CHL) in patients (pts) with TS is due to recurrent otitis media with effusion, chronic middle ear infection, and cholesteatoma probably as the result of malfunction of the Eustachian tube associated with lymphedema and anatomic shortening of the skull base. The high prevalence of middle ear infections and CHL...
Objective: Recent reports have suggested a significant incidence of sensorineural hearing loss (SNHL...
Introduction: Turner syndrome is a frequent genetic disorder that affects female individuals and cov...
Thorough descriptions of genotype-phenotype correlations in genetic hearing impairment facilitates a...
Turner syndrome (TS) is one of the most common chromosomal abnormalities, occurring in about 50 per ...
Turner syndrome (TS) is one of the most common chromosomal abnormalities, occurring in about 50 per ...
Turner syndrome (TS) is one of the most common chromosomal abnormalities, occurring in about 50 per ...
Turner syndrome (TS) is one of the most common chromosomal abnormalities, occurring in about 50 per ...
Turner Syndrome is a common chromosomal disorder and affects approximately one in every 2000 newborn...
The purpose of this article was to evaluate otological diseases in 173 patients (pts) with Turner sy...
The purpose of this article was to evaluate otological diseases in 173 patients (pts) with Turner sy...
The purpose of this article was to evaluate otological diseases in 173 patients (pts) with Turner sy...
The purpose of this article was to evaluate otological diseases in 173 patients (pts) with Turner sy...
The purpose of this article was to evaluate otological diseases in 173 patients (pts) with Turner sy...
INTRODUCTION: Turner's syndrome (TS) is caused by a partial or total deletion of an X chromosome, o...
AbstractIntroductionturner's syndrome (TS) is caused by a partial or total deletion of an X chromoso...
Objective: Recent reports have suggested a significant incidence of sensorineural hearing loss (SNHL...
Introduction: Turner syndrome is a frequent genetic disorder that affects female individuals and cov...
Thorough descriptions of genotype-phenotype correlations in genetic hearing impairment facilitates a...
Turner syndrome (TS) is one of the most common chromosomal abnormalities, occurring in about 50 per ...
Turner syndrome (TS) is one of the most common chromosomal abnormalities, occurring in about 50 per ...
Turner syndrome (TS) is one of the most common chromosomal abnormalities, occurring in about 50 per ...
Turner syndrome (TS) is one of the most common chromosomal abnormalities, occurring in about 50 per ...
Turner Syndrome is a common chromosomal disorder and affects approximately one in every 2000 newborn...
The purpose of this article was to evaluate otological diseases in 173 patients (pts) with Turner sy...
The purpose of this article was to evaluate otological diseases in 173 patients (pts) with Turner sy...
The purpose of this article was to evaluate otological diseases in 173 patients (pts) with Turner sy...
The purpose of this article was to evaluate otological diseases in 173 patients (pts) with Turner sy...
The purpose of this article was to evaluate otological diseases in 173 patients (pts) with Turner sy...
INTRODUCTION: Turner's syndrome (TS) is caused by a partial or total deletion of an X chromosome, o...
AbstractIntroductionturner's syndrome (TS) is caused by a partial or total deletion of an X chromoso...
Objective: Recent reports have suggested a significant incidence of sensorineural hearing loss (SNHL...
Introduction: Turner syndrome is a frequent genetic disorder that affects female individuals and cov...
Thorough descriptions of genotype-phenotype correlations in genetic hearing impairment facilitates a...