Nephronophthisis (NPHP) & Related Rare Cystic Kidney Diseases
Tune-in to the NephU webinar where we are joined by experts, Carl Bates, MD and Rannar Airik, PhD who will describe nephronophthisis (NPHP), the most frequent genetic cause for end-stage kidney disease in the first three decades of life, and its associated rare genetic syndromes such as Senior-Løken Syndrome (SLNS), Joubert Syndrome (JSRD), Meckel Syndrome (MKS), and Bardet-Biedl Syndrome (BBS).