GLDC-related glycine encephalopathy (GLDC-related GE) is a disease that impairs the body's ability to metabolize glycine, an amino acid found in proteins. Glycine accumulates in all body tissues, including the brain, and can lead to lethargy, seizures, low muscle tone, apnea, coma, and often death. Patients who survive with GLDC-related GE have intellectual disability and seizures. The majority of patients with GLDC-related encephalopathy present in the neonatal period, but there are multiple forms of the condition described.
The neonatal form of this disease presents in the first hours to days of life with rapid progression of symptoms. The infantile onset form is characterized by developmental delays and infantile-onset seizures at approximately 6 months of age. Other atypical types of GLDC-related GE appear later in childhood or adulthood and cause a variety of medical problems that primarily affect the nervous system.
Glycine encephalopathy affects approximately 1 in 250,000 live births in the United States. At least 50% of cases worldwide result from mutations in the GLDC gene (may vary by region). However, studies suggest that the incidence of glycine encephalopathy is higher in certain populations such as Finland (1 in 55,000, almost exclusively a result of GLDC mutations) and British Columbia (1 in 63,000, mainly a result of GLDC mutations).
There is no treatment GLDC-related glycine encephalopathy. Disease management is aimed at trying to reduce the accumulation of glycine in the body. Glycine plasma concentrations can be reduced by sodium benzoate and low protein diet. Seizures are addressed with anticonvulsant medications, but may not be completely effective for all individuals.
About 85% of those with neonatal onset and 50% of those with the infantile onset will have severe symptoms. These infants typically will have profound intellectual disability and will have seizures that are difficult to treat. Death in the first year is common in these individuals.
Approximately 20% of all children affected with glycine encephalopathy will have less severe symptoms. These individuals will have moderate intellectual disability. They are often able to communicate (most often non-verbally), and typically have seizures that respond to treatment. These children may develop movement disorders and behavioral problems.
Rarely, affected individuals present with late-onset glycine encephalopathy, in which symptoms appear usually after one year of age. These individuals typically have some intellectual disability and seizures are uncommon.
Explanations of an extensive number of genetic diseases written for the public by the U.S. government's National Institutes of Health.
NKH International Family Network's goal is to connect families, and provide support and knowledge to anyone affected by the metabolic condition nonketotic hyperglycinemia or glycine encephalopathy, as it is also referred to.
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