RAS gene mutations linked to autosomal recessive renal tubular dysgenesis

Rachael Williams

This article has no abstract so we have provided the first paragraph of the full text.

According to a recent study, genetic defects in the renin–angiotensin system (RAS) are linked to, and could be the fundamental cause of, autosomal recessive renal tubular dysgenesis (RTD), a severe fetal disorder of kidney development associated with anuria, hypotension and perinatal death. This important discovery might eventually aid early prenatal diagnosis and present genetic counseling opportunities for affected families.

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