GLYT1 encephalopathy
GLYT1 encephalopathy is a rare autosmal recessive, metabolic and genetic disorder which is caused by a mutation in the SLC6A9 gene.
The main features of this disorder are: severely diminished muscle tone, respiratory failure, absence of neonatal reflexes, encephalopathy, reduced consciousness and unresponsiveness, also it can present with arthrogryposis/ligament laxity, and normal serum glycine.
About 10 cases had been reported as of 2022.
Symptoms
Someone with GLYT1 encephalopathy can present with facial dysmorphism, arthrogryposis and diminished muscle tone that progresses into muscle hypertonicity with so called startle-like clonus and normal serum glycine level.Facial features of this disorder might include: thin eyebrows, saddle nose, retrognathism, long myopathic face, piggy noses, tent-shaped mouth, low-set ears.
Diagnosis
Diagnosis of this disorder can be suspected by symptoms and by high glycine levels in cerebrospinal fluid and normal levels of enzymes and glycine in plasma, consequently diagnosis can be confirmed by genetic testing of GLYT1.Cause
This disorder is caused by a mutation in a gene SLC6A9, which encodes Sodium- and chloride-dependent glycine transporter 1 protein, which is located on chromosome 1.Pathophysiology
Glycine is the simplest amino acid, that doesn't have any stereoisomers. Glycine participates in protein synthesis, but it can act as neurotransmitter, in the spinal cord and in the brain stem, it acts as inhibitory neurotransmitter by activating glycine channels. Although it has excitatory effect in neocortex.GLYT1 protein is located on astrocytes that are next to glycinergic neurons to clear glycine swiftly from the synaptic cleft. Consequently, this mechanism is disrupted in this disease by hyperactivating NMDA receptors and glycine receptors.