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Central and gonadal hypogonadism in X-linked lissencephaly
Isil Halac1, Reema Habiby, John Curran
1Pediatric Endocrinology, Children's Memorial Hospital, Northwestern University, Chicago, IL, USA. ihalac@childrensmemorial.org
Objective:
To directly test gonadal function in a patient with X-linked lissencephaly with ambiguous genitalia (XLAG) in light of lack of previous functional data.
Study Design And Results:
We studied an infant who failed to increase testosterone levels in response to hCG stimulation.
Conclusion:
In XLAG, the gonads are not only structurally dysgenetic but also functionally abnormal.
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