Familial (9;11)(p22;p15.5)pat translocation and XX sex reversal in a phenotypic boy with cryptorchidism and delayed development.

Article

Familial (9;11)(p22;p15.5)pat translocation and XX sex reversal in a phenotypic boy with cryptorchidism and delayed development.

Genetic counseling (Geneva, Switzerland) - 1 Jan 2004

Prabhakara K, Angalena R, Ramadevi A Radha

Abstract excerpt

We describe a patient with the co-occurrence of a familial 9;11 reciprocal translocation and an XX sex reversal. The patient had cryptorchidism, delayed development, dysmorphic features and attention deficiency hyperactive disorder (ADHD). The proband's karyotype was 46,XX,t(9;11)(p22;p15.5) and...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Familial (9;11)(p22;p15.5)pat translocation and XX sex reversal in a phenotypic boy with cryptorchidism and delayed development.

Abstract excerpt

Topics

Related research