¿Cómo se diagnostica el Síndrome 48,XXYY?

Cómo se diagnostica Síndrome 48,XXYY: pruebas, especialistas y el camino hasta el diagnóstico, contado por pacientes y revisado con fuentes.

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My initial diagnosis was of low testosterone via a blood test. I was then referred to an Endocrinologist who examined me and thought by my physical attributes that I may have KS.

I was then referred to Guys Hospital in London for a genetic test - whereby 3 weeks after the test it was confirmed that I had KS / Primary Hypogonadism.

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