Children’s Hospital physicians said the new drug therapy, Zolgensma, is a revolution in neurological pediatric care.
“This therapy represents a new opportunity for us to intervene and change children’s long-term prospects, and sometimes if we can treat the disease in time, we can restore them to full health,” said David Michelson, MD, chief of the division of child neurology and director of the pediatric muscular dystrophy association clinics at Children’s Hospital. “This therapy is a chance to wipe a patient’s health slate clean.”
The patient was diagnosed with SMA through the state of California’s newborn screening program. Even though the patient seemed perfectly healthy during the first weeks of life, the healthcare team was working against the clock to treat the patient before the first potential onset of symptoms. Studies have shown that infants who receive the therapy as soon after diagnosis as possible have better outcomes than those who receive delayed treatment.
SMA is a rare genetic disease that causes a person’s muscles to weaken and become smaller over time. In an infant, this affects development, including crawling, walking, sitting, and head control. Severe types of SMA affect the muscles used for swallowing and breathing and, untreated, lead to ventilator dependence and a high risk of mortality.
According to Michelson, the patient’s neurologist, there are four types of SMA. These types differ in both their severity and at what age they will manifest in a person’s body. SMA type I, the most common of the severe forms, can present in infants as early as three months and is often fatal by the age of two.