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Annales d'Endocrinologie
Volume 71, n° 3
pages 158-162 (mai 2010)
Doi : 10.1016/j.ando.2010.02.024
Congenital hypogonadotropic hypogonadism in females: Clinical spectrum, evaluation and genetics
Hypogonadisme hypogonadotrope chez la femme : clinique, exploration et diagnostic génétique

Fig. 1

Fig. 1 : 

Distribution by sex of patients evaluated for congenital hypogonadotropic hypogonadism at the Endocrinology and Reproduction Department, Bicêtre Teaching Hospital. (update :march 2010)

Fig. 2

Fig. 2 : 

Complete congenital hypogonadotropic hypogonadism in a 22-year-old woman referred for primary amenorrhea.

Fig. 3

Fig. 3 : 

Steps to overcome before achieving the diagnosis of congenital hypogonadotropic hypogonadism (CHH) in women or female teenagers referred for primary amenorrhea.

Fig. 4

Fig. 4 : 

Molecular studies proposed at the Endocrinology and Reproduction Department, Bicêtre Teaching Hospital to females with CHH categorized on the basis of sense of smell.

Fig. 5

Fig. 5 : 

Genotype–phenotype relationship in women with normosmic non syndromic CHH caused by GnRH receptor loss of function mutations. Adapted from [1].

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