What does GCE mean in HOSPITALS

Glycine encephalopathy affects people of all ages, but it is most commonly seen in infants and young children. It is estimated that one out of every 250,000 to 350,000 births worldwide will have this condition.

To diagnose glycine encephalopathy, doctors usually use genetic testing to look for the mutations associated with the disorder. Additional tests such as urine analysis or biochemistry profiles may also be necessary to assess levels of glycine in the blood stream.

Unfortunately there is no cure for glycine encephalopathy at this time. Treatment options are symptomatic and supportive, aiming to reduce complications related to the condition and improve quality of life. These may include dietary interventions (low-protein diet), medications (anticonvulsants), physical therapy and speech therapy.

Yes. If someone has been diagnosed with glycine encephalopathy, then any siblings or future children have a risk of inheriting it from them as it is an autosomal recessive condition which means both parents must carry the gene mutation for it to be transferred on to their offspring.

Dietary changes may be recommended by your doctor to help manage symptom severity associated with glycene encephalopathy including restricting protein intake limiting tyrosinosis-containing foods like apples or dried plums or supplementing certain amino acids like L-Carnitide.

Physical therapy can be beneficial for individuals living with glysinemia as it can help improve strength and coordination while encouraging independence through activities such as repetitive exercises which strengthen muscle memory. Additionally it can teach kids how to use mobility aids such as walkers or wheelchairs.