Garrod's tetrad
Garrod's tetrad is a medical condition named after the British physician Archibald Garrod, who first described it. It is characterized by four main symptoms: albinism, mental retardation, spasticity, and myoclonus.
Symptoms[edit | edit source]
The four main symptoms of Garrod's tetrad are:
- Albinism: This is a condition in which there is a lack of pigment in the skin, hair, and eyes. It can result in vision problems and an increased risk of skin cancer.
- Mental retardation: This is a term used to describe below-average intelligence and set of life skills. It is usually present from birth and affects a person's everyday social and practical skills.
- Spasticity: This is a condition in which certain muscles are continuously contracted. This contraction causes stiffness or tightness of the muscles and can interfere with normal movement, speech, and gait.
- Myoclonus: This is a condition in which a person has quick, involuntary muscle jerks. They are often seen in people with neurological disorders.
Causes[edit | edit source]
Garrod's tetrad is a genetic disorder. It is caused by mutations in the gene that produces the enzyme homogentisate 1,2-dioxygenase. This enzyme is involved in the breakdown of amino acids, the building blocks of proteins. When this enzyme is missing or not working properly, a substance called homogentisic acid builds up in the body and can cause damage to various tissues and organs.
Diagnosis[edit | edit source]
The diagnosis of Garrod's tetrad is based on the presence of the four main symptoms. Genetic testing can confirm the diagnosis.
Treatment[edit | edit source]
There is currently no cure for Garrod's tetrad. Treatment is focused on managing the symptoms and improving the quality of life for those affected. This may include physical therapy for spasticity, medications to control myoclonus, and special education services for mental retardation.
See also[edit | edit source]
Garrod's tetrad Resources | |
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