by Peter Ciszewski | Mar 10, 2021
Melanie McKay, mother of a young boy with infantile-onset Pompe disease talks about the importance of having a clinician listen to the caregiver of the child. Pompe disease is a rare inherited lysosomal storage disorder due to low levels of acid...
by Peter Ciszewski | Mar 10, 2021
Francesca Fumagalli, PhD, Researcher of Cardiovascular Medicine at Istituto di Ricerche Farmacologiche Mario Negri (IRCCS), discusses positive results of a study of lentiviral hematopoietic stem cell gene therapy for the treatment of metachromatic...
by Peter Ciszewski | Mar 9, 2021
Emily Holtvluwer, mother of two young children with spinal muscular atrophy (SMA), discusses the two different diagnostic journeys her kids went through to get a diagnosis. Her oldest child was not diagnosed for several months after symptoms began to appear...
by Peter Ciszewski | Mar 8, 2021
Damara Ortiz, MD, FAAP, FACMG, Assistant Professor of Pediatrics and Director of the Lysosomal Storage Disorders Program at UPMC Children’s Hospital of Pittsburgh, discusses why the process of newborn screening for lysosomal storage disorders can be so...
by Peter Ciszewski | Mar 5, 2021
Priya Kishnani, MD, Professor of Pediatrics at the Duke University School of Medicine, discusses the benefits that newborn screening for Pompe disease can provide for both the patient and research community. Pompe disease is a rare inherited lysosomal storage...
