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Phenotypic variations in X chromosome mutations: Two case reports

DOI: 10.1016/j.crwh.2018.e00084

Keywords: Turner variant, X chromosome mutation

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Abstract:

Turner syndrome (TS) affects 1 in 2500 females. Monosomy X is the most common etiology, classically presenting with hypoestrogenemia and short stature. We present two cases of partial X chromosome deletions that do not reflect the typical phenotype of TS

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