About glutaricacidemia i
What is glutaricacidemia i?
Glutaricaciduria I (GA-I) is a rare hereditary metabolic disorder, caused by a deficiency of the enzyme glutaryl-CoA dehydrogenase. One of a group of disorders known as "organic acidemias," it is characterized by an enlarged head (macrocephaly), decreased muscle tone (hypotonia), vomiting, and excess acid in the blood. Affected individuals may also have involuntary movements of the trunk and limbs (dystonia or athetosis) and mental retardation may also occur.
Babies with glutaricaciduria I are sometimes mistakenly thought by medical professionals to be abused babies because they present with subdural and/or retinal hemorrhages.
What are the symptoms for glutaricacidemia i?
Babies with GA1 are born healthy and may only present with unspecific signs like macrocephaly at birth. Macrocephaly is one of the earliest signs of GA1 so newborns with an enlarged head circumference should be evaluated for GA1. Especially during the age of 3 months until 3 years, most affected babies develop an acute encephalopathic crisis which is triggered by catabolic conditions such as febrile infections, febrile reactions to vaccinations or surgery. These crises result in striatal injury and a complex, mostly dystonic, irreversible and severe movement disorder which is associated with high morbidity and mortality. These babies can experience several symptoms resembling those of cerebral palsy, such as frequently assuming odd positions due to disordered muscle tone (dystonia), involuntary and ceaseless slow, sinuous, writhing (athetotic) or jerky (choreic) movements of the trunk and limbs. Controlling the movement of hands, arms, feet, legs, head, and neck may become very hard and muscle spasms may occur. Repeated stress on the body (such as infection and Fever) can cause symptoms to worsen, but in some children, brain damage will occur without a triggering Fever. Mild to moderate intellectual disabilities may also accompany these symptoms, but some studies have shown that the intellectual ability of a person with GA1, even if untreated, is not or only mildly affected.
In recent years, also other neurologic disease manifestations have been reported such as chronic kidney disease.
For 80-90% of people with GA1, motor symptom development is preventable, but this requires early diagnosis by newborn screening and treatment from birth on. Treatment consists of a low lysine diet and oral carnitine supplementation as well as intermittent emergency treatment during episodes that are likely to induce catabolism. If treatment is delayed or inadequate, motor symptoms begin to manifest acutely or insidiously during infancy or early childhood (before the age of 6) and are often highly variable. A minority of GA1 patients is diagnosed lately in adolescence or even adult age, following the diagnostic work-up of unspecific neurologic symptoms.
If GA1 is not treated, most patients experience an “acute encephalopathic crisis” following preceding trigger symptoms such as:
- Nausea, Vomiting, Diarrhea
- Hypotonia (low muscle tone)
- Poor appetite or difficulty feeding
- Lack of energy/sleepy
- Muscle Weakness
Possible irreversible neurologic symptoms of an acute encephalopathic crisis are
- Dyskinesia-disorder of involuntary muscle movements
- Dystonia – fixed abnormal postures due to abnormally increased muscle tone
- Orofacial dyskinesia
- Choreoathetosis—irregular migrating contractions, twisting, writhing
- Abnormality of eye movement- nystagmus (involuntary shaking of the eyes)
- Cognitive impairment (highly variable and not seen in many patients)
- Developmental regression
- Opisthotonus- full body spasms
Other possible symptoms noted:
- Intracranial hemorrhage- bleeding in brain
- Neurological speech impairment
- Dilation of the lateral ventricles of brain
What are the causes for glutaricacidemia i?
GA1 is caused by changes (mutations) in the GCDH gene that leads to deficiency of the enzyme, glutaryl-CoA dehydrogenase or GCDH. This enzyme is responsible for metabolizing the amino acids lysine, hydroxylysine, and tryptophan. Mutations in the GCDH gene prevent production of the enzyme resulting in abnormal levels of glutaric, 3-hydroxyglutaric and (to a lesser extent) glutaconic acids These products accumulate and cause damage to an area of the brain called the basal ganglia that regulates motor movement.
GA1 is inherited as an autosomal recessive genetic condition. Recessive genetic disorders occur when an individual inherits a non-working gene from each parent. If an individual receives one working gene and one non-working gene for the disease, the person will be a carrier for the disease, but usually will not show symptoms. Both parents of a patient are carriers in autosomal-recessive conditions. The risk for two carrier parents to both pass the non-working gene and, therefore, have an affected child is 25% with each pregnancy. The risk to have a child who is a carrier, like the parents, is 50% with each pregnancy. The chance for a child to receive working genes from both parents is 25%. The risk is the same for males and females.
What are the treatments for glutaricacidemia i?
Today, GA-I is considered to be a treatable condition. Metabolic treatment consists of a low lysine diet with supplementation of a lysine-free, trytophane-reduced, amino acid mixture, oral supplementation of L-carnitine and an intensified emergency treatment during episodes of intercurrent illness or surgical interventions. It has been recommended by an international guideline group for all patients up to 6 year.
Children with GA1 can develop normally if a thorough treatment plan is followed properly, but treatment must begin from a very early age (from the newborn period before symptoms occur and onwards). If not promptly and properly treated, GA1 will typically cause serious, irreversible, neurologic damage that can permanently affect control of voluntary muscle movement and can severely impact life and shorten life expectancy, especially if damage occurs before the age of 6.
Long-term outcome is still incompletely understood, neurologic disease or extracerebral manifestation like chronic kidney disease may occur in adulthood and variable extrastriatal MRI changes may progress after age 6 years. Therefore, protein control using natural protein with a low lysine content and avoidance of lysine-rich food is advisable after age 6 years.
Genetic counseling is recommended for families of children with GA1.
Is there a cure/medications for glutaricacidemia i?
Glutaric acidemia I is a rare and severe inherited condition that makes the body unable to digest certain types of protein ( amino acids). This results in organic acid disorder that results in an abnormal buildup of organic acid in blood and urine. Moreover, the tissues of the body can also be intoxicated and serve health problems like brain damage, kidney, and liver failure.
People with Glutaric acidemia I lack particular enzymes in the body that breaks the amino acid-like hydroxylysine, lysine, and tryptophan, which are building blocks of protein.
Moreover, This can be treated through the following method:
- Dietician: the child should have a diet specialist in order to monitor the protein intake of the baby in the body. However, the mother milk consumed by the baby should be examined by the dietician.
- Low protein diet: The child is affected by the improper digestion of amino acids and protein, which can mix up the blood and show hazardous results in the blood. To avoid such a situation, the child should be given a low protein and high calories diet that keep him full for longer.
- L-carnitine: it is a dietary supplement that breaks long-chain amino acids and converts them into energy. Adding L-carnitine to the diet strengthens the metabolism to break down protein and convert that into energy.
- Avoid certain foods: meat, fish, cheese, eggs, pulses, nuts, and seeds should be avoided because these are rich in protein.
Spasms,Jerking,Rigidity, or decreased muscle tone,Bleeding in the brain or eyes,Neurological damage,Stress
Low protein diet,Diet restriction,L-carnitine
Breathing difficulties,Lack of energy,Abnormal movements,Vomiting,Irritability