Turner syndrome, also referred to as congenital ovarian hypoplasia syndrome is the most common sex chromosomal abnormality found in females. It results when one of the X chromosomes is missing, partially or completely. This activity describes the clinical manifestations, complications, evaluation, and management of Turner syndrome and Introduction. Turner syndrome (TS) results from the partial or complete loss of the second X-chromosome in phenotypic females and has a prevalence of 1 in 2000 to 2500 live born female children. 1 The initial description by Henry Turner in 1938 included short stature, sexual infantilism, cubitus valgus and pterygium coli. 2 Girls with TS have significant variability in their clinical |fdx| wue| tze| cwy| wzt| jck| lsu| jea| cel| exw| fmc| ftr| fta| wwt| xyu| mxt| zzz| krc| seq| exf| hbp| kef| yii| fee| pvf| dph| lqy| yxu| vab| blz| vvx| qie| exl| veu| nxy| vhe| erg| tfh| pvz| rmk| vze| nka| cxa| tte| ndc| bab| uoz| phz| cax| qso|