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Potential disadvantages of the new classification include [10] : 1 The karyotype might vary among individuals with the same condition. Medical treatment with life-long cortisone replacement after birth is mandatory. Long-term followup and comparison between genotype and phenotype in 29 cases of complete androgen insensitivity syndrome. Please review our privacy policy. Table 2 Gonadal malignancy risks in different DSD conditions. Affected individuals have normal female external genitalia but fail to develop secondary sexual characteristics [4]. Phenotypically, patients are normal, tall and hairless females with feminine external genitalia and a very short and shallow utricle Figure 4. Before the seventh week of gestation both XX and XY foetuses have an identical reproductive anatomy.

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