Encyclopedia
Gyrate atrophy of the choroid and retina, which is often shortened to gyrate atrophy, is an inherited disorder characterized by progressive vision loss. People with this disorder have an ongoing loss of cells (atrophy) in the retina, which is the specialized light-sensitive tissue that lines the back of the eye, and in a nearby tissue layer called the choroid. During childhood, they begin experiencing nearsightedness (myopia), difficulty seeing in low light (night blindness), and loss of side (peripheral) vision. Over time, their field of vision continues to narrow, resulting in tunnel vision. Many people with gyrate atrophy also develop clouding of the lens of the eyes (cataracts). These progressive vision changes lead to blindness by about the age of 50.
- genetic conditions
1. Introduction
Most people with gyrate atrophy have no symptoms other than vision loss, but some have additional features of the disorder. Occasionally, newborns with gyrate atrophy develop excess ammonia in the blood (hyperammonemia), which may lead to poor feeding, vomiting, seizures, or coma. Neonatal hyperammonemia associated with gyrate atrophy generally responds quickly to treatment and does not recur after the newborn period.
Gyrate atrophy usually does not affect intelligence; however, abnormalities may be observed in brain imaging or other neurological testing. In some cases, mild to moderate intellectual disability is associated with gyrate atrophy.
Gyrate atrophy may also cause disturbances in the nerves connecting the brain and spinal cord to muscles and sensory cells (peripheral nervous system). In some people with the disorder these abnormalities lead to numbness, tingling, or pain in the hands or feet, while in others they are detectable only by electrical testing of the nerve impulses.
In some people with gyrate atrophy, a particular type of muscle fibers (type II fibers) break down over time. While this muscle abnormality usually causes no symptoms, it may result in mild weakness.
2. Frequency
More than 150 individuals with gyrate atrophy have been identified; approximately one third are from Finland.
3. Causes
Mutations in the OAT gene cause gyrate atrophy. The OAT gene provides instructions for making the enzyme ornithine aminotransferase. This enzyme is active in the energy-producing centers of cells (mitochondria), where it helps break down a molecule called ornithine. Ornithine is involved in the urea cycle, which processes excess nitrogen (in the form of ammonia) that is generated when protein is broken down by the body. In addition to its role in the urea cycle, ornithine participates in several reactions that help ensure the proper balance of protein building blocks (amino acids) in the body. This balance is important because a specific sequence of amino acids is required to build each of the many different proteins needed for the body's functions. The ornithine aminotransferase enzyme helps convert ornithine into another molecule called pyrroline-5-carboxylate (P5C). P5C can be converted into the amino acids glutamate and proline.
OAT gene mutations that cause gyrate atrophy result in a reduced amount of functional ornithine aminotransferase enzyme. A shortage of this enzyme impedes the conversion of ornithine into P5C. As a result, excess ornithine accumulates in the blood (hyperornithinemia), and less P5C than normal is produced. It is not clear how these changes result in the specific signs and symptoms of gyrate atrophy. Researchers have suggested that a deficiency of P5C may interfere with the function of the retina. It has also been proposed that excess ornithine may suppress the production of a molecule called creatine. Creatine is needed for many tissues in the body to store and use energy properly. It is involved in providing energy for muscle contraction, and it is also important in nervous system functioning.
4. Inheritance
This condition is inherited in an autosomal recessive pattern, which means both copies of the gene in each cell have mutations. The parents of an individual with an autosomal recessive condition each carry one copy of the mutated gene, but they typically do not show signs and symptoms of the condition.
5. Other Names for This Condition
- gyrate atrophy
- HOGA
- hyperornithinemia with gyrate atrophy of choroid and retina
- OAT deficiency
- OKT deficiency
- ornithine aminotransferase deficiency
- ornithine keto acid aminotransferase deficiency
- ornithine-delta-aminotransferase deficiency
- Ornithinemia with gyrate atrophy
This entry is adapted from the peer-reviewed paper https://medlineplus.gov/genetics/condition/gyrate-atrophy-of-the-choroid-and-retina
References
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- Heinänen K, Näntö-Salonen K, Komu M, Erkintalo M, Heinonen OJ, Pulkki K,Valtonen M, Nikoskelainen E, Alanen A, Simell O. Muscle creatine phosphate ingyrate atrophy of the choroid and retina with hyperornithinaemia--clues topathogenesis. Eur J Clin Invest. 1999 May;29(5):426-31.
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- Peltola KE, Jääskeläinen S, Heinonen OJ, Falck B, Näntö-Salonen K, Heinänen K,Simell O. Peripheral nervous system in gyrate atrophy of the choroid and retinawith hyperornithinemia. Neurology. 2002 Sep 10;59(5):735-40.
- Peltola KE, Näntö-Salonen K, Heinonen OJ, Jääskeläinen S, Heinänen K, SimellO, Nikoskelainen E. Ophthalmologic heterogeneity in subjects with gyrate atrophy of choroid and retina harboring the L402P mutation of ornithine aminotransferase.Ophthalmology. 2001 Apr;108(4):721-9.
- Santinelli R, Costagliola C, Tolone C, D'Aloia A, D'Avanzo A, Prisco F,Perrone L, del Giudice EM. Low-protein diet and progression of retinaldegeneration in gyrate atrophy of the choroid and retina: a twenty-six-yearfollow-up. J Inherit Metab Dis. 2004;27(2):187-96.
- Shenoi A, L N, Christopher R. Hyperornithinemia associated with gyrate atrophyof the choroid and retina in a child with myopia. Indian Pediatr. 2001Aug;38(8):914-8.
- Valtonen M, Näntö-Salonen K, Jääskeläinen S, Heinänen K, Alanen A, HeinonenOJ, Lundbom N, Erkintalo M, Simell O. Central nervous system involvement ingyrate atrophy of the choroid and retina with hyperornithinaemia. J Inherit MetabDis. 1999 Dec;22(8):855-66.
