Ocular coloboma
- PMID: 6782689
- DOI: 10.1016/0039-6257(81)90092-8
Ocular coloboma
Abstract
Ocular coloboma is common malformation which includes a spectrum of anomalies that ranges from iris coloboma to clinical anophthalmos. Coloboma is etiologically heterogeneous. As an isolated defect, it is usually inherited as an autosomal dominant disorder, although autosomal recessive inheritance also occurs. Patients with multiple malformations and coloboma may have a recognized malformation syndrome of unknown etiology, a single gene disorder, or chromosomal abnormality. Prognosis and recurrence risk can be determined only after complete evaluation of the patient and other family members.
Similar articles
-
Colobomatous malformations of the ocular globe.Int Ophthalmol Clin. 1968 Winter;8(4):797-816. Int Ophthalmol Clin. 1968. PMID: 4984821 No abstract available.
-
Hereditary colobomatous anomalies of the optic nerve head.Ophthalmic Paediatr Genet. 1986 Aug;7(2):127-30. doi: 10.3109/13816818609076121. Ophthalmic Paediatr Genet. 1986. PMID: 3785881
-
Possible autosomal-recessive ocular coloboma.Am J Med Genet. 1981;9(3):189-93. doi: 10.1002/ajmg.1320090304. Am J Med Genet. 1981. PMID: 7282780
-
Genetics of microphthalmos.Int Ophthalmol. 1981 Aug;4(1-2):45-65. doi: 10.1007/BF00139580. Int Ophthalmol. 1981. PMID: 6795139 Review.
-
[Ocular signs of trisomy 13. General review].Adv Ophthalmol. 1971;24(0):174-202. Adv Ophthalmol. 1971. PMID: 5006098 Review. French. No abstract available.
Cited by
-
Surgical outcome of 21 patients with congenital upper eyelid coloboma.Int J Ophthalmol. 2010;3(1):69-72. doi: 10.3980/j.issn.2222-3959.2010.01.16. Epub 2010 Mar 18. Int J Ophthalmol. 2010. PMID: 22553521 Free PMC article.
-
Retinal dystrophy and macular coloboma.Doc Ophthalmol. 1988 Mar-Apr;68(3-4):257-71. doi: 10.1007/BF00156432. Doc Ophthalmol. 1988. PMID: 3042323 Review.
-
Mutations in crystallin genes result in congenital cataract associated with other ocular abnormalities.Mol Vis. 2017 Dec 24;23:977-986. eCollection 2017. Mol Vis. 2017. PMID: 29386872 Free PMC article.
-
Ocular presentation of Walker-Warburg syndrome with POM2 mutation.Indian J Ophthalmol. 2022 Jul;70(7):2626-2627. doi: 10.4103/ijo.IJO_2128_21. Indian J Ophthalmol. 2022. PMID: 35791178 Free PMC article. No abstract available.
-
Familial exudative vitreoretinopathy in a patient with choroidal coloboma.BMJ Case Rep. 2019 Mar 6;12(3):e228711. doi: 10.1136/bcr-2018-228711. BMJ Case Rep. 2019. PMID: 30846457 Free PMC article. No abstract available.
Publication types
MeSH terms
Grants and funding
LinkOut - more resources
Full Text Sources
Research Materials