Disorders/differences of sex development (DSD) are difficult to diagnose because of the multiple phenotypes and genes involved, but a new technique developed at Hudson Institute of Medical Research is set to change all that.
Understanding DSD
About one in 5000 babies is born with DSD or intersex, where their genetic, hormonal or physical sex characteristics (genitals, gonads and chromosome patterns) are not typically male or female.
Until now diagnosing the cause of many DSDs has been hampered because the events that determine sex development occur at around week nine of gestation and only in a small number of cells of the gonads of the developing fetus.
But Professor Vincent Harley and his team have developed a model to study this through reprogramming skin cells into testicular cells (Sertoli cells) to understand the changed cell and genetic processes that lead to the Intersex condition in that patient.
"We study the genes involved in formation of the testis in the embryo, but our understanding of this process is limited by the obvious problems in obtaining human samples. So we developed a way of transforming skin cells into the key cells of the testis, the Sertoli cells, which we can then grow and analyse," he said.
Simpler sex development disorder diagnosis critical
Their research, published in the journal Biology of Sex Differences, shows how this technique can address the lack of availability of gonadal tissue from patients at specific developmental stages by allowing diagnostics tests to be carried out on reprogrammed skin cells.
Prof Harley explains: "Sertoli cells are relevant because they act like an organising centre of embryonic gonadal development and many DSDs arise when these developmental processes go awry."
"Accurate diagnosis is critical to inform the occurrence of life-threatening crises (e.g. congenital adrenal hyperplasia), the response to hormone replacement therapy, eventual gender identity, cancer risk and counselling for future fertility."
"Patients suffer a long diagnostic odyssey, with many never receiving a definitive diagnosis," Prof Harley said. "Our new model will help Identify new causes and mechanisms of DSD in children."
