» Articles » PMID: 6795139

Genetics of Microphthalmos

Overview
Journal Int Ophthalmol
Specialty Ophthalmology
Date 1981 Aug 1
PMID 6795139
Citations 11
Authors
Affiliations
Soon will be listed here.
Abstract

This is a survey of the genetics of microphthalmos and the heritable syndromes in which microphthalmos occurs. New syndromes are delineated such as the autosomal dominant anophthalmos-microphthalmos-coloboma syndrome, the autosomal dominant microphthalmos, microcephaly, lacunar retinal atrophy syndrome, the autosomal recessive anophthalmos-microphthalmos-coloboma syndrome, the autosomal recessive syndrome with anophthalmos or microphthalmos and genital malformations, and the autosomal recessive syndrome with microphthalmos, microcephaly and retinal falciform folds. Nanophthalmos is described as a poorly defined phenotype and rejected as a genotype. Several other genetic entities with microphthalmos are reviewed and recent descriptions are surveyed.

Citing Articles

Chronic central serous choroidopathy with severe visual loss in hyperopic microphthalmic identical twins.

Fabry A, Blanckaert J, Leys A GMS Ophthalmol Cases. 2016; 1:Doc05.

PMID: 27625927 PMC: 5015606. DOI: 10.3205/oc000005.


Atypical features of nanophthalmic macula--a spectral domain OCT study.

Rao A, Padhi T, Jena S, Mandal S, Das T BMC Ophthalmol. 2012; 12:12.

PMID: 22672150 PMC: 3441246. DOI: 10.1186/1471-2415-12-12.


Developmental basis of nanophthalmos: MFRP Is required for both prenatal ocular growth and postnatal emmetropization.

Sundin O, Dharmaraj S, Bhutto I, Hasegawa T, McLeod D, Merges C Ophthalmic Genet. 2008; 29(1):1-9.

PMID: 18363166 PMC: 2739627. DOI: 10.1080/13816810701651241.


[Treatment of congenital clinical anophthalmos with high hydrophilic hydrogel expanders].

Schittkowski M, Gundlach K, Guthoff R Ophthalmologe. 2003; 100(7):525-34.

PMID: 12920552 DOI: 10.1007/s00347-002-0776-9.


The nanophthalmic macula.

Serrano J, Hodgkins P, Taylor D, Gole G, Kriss A Br J Ophthalmol. 1998; 82(3):276-9.

PMID: 9602624 PMC: 1722527. DOI: 10.1136/bjo.82.3.276.


References
1.
Kapoor S, Kapoor M . Congenital ocular anomalies in Pondicherry. J Pediatr Ophthalmol. 1977; 14(6):382-9. View

2.
De Jong J, DELLEMAN J, Houben M, MANSCHOT W, DE MINJER A, Mol J . Agenesis of the corpus callosum, infantile spasms, ocular anomalies (Aicardi's syndrome). Clinical and pathologic findings. Neurology. 1976; 26(12):1152-8. DOI: 10.1212/wnl.26.12.1152. View

3.
SUGAR H, Thompson J, Davis J . The oculo-dento-digital dysplasia syndrome. Am J Ophthalmol. 1966; 61(6):1448-51. DOI: 10.1016/0002-9394(66)90484-3. View

4.
Lindstedt E . Congenital malformations of the eye. Report on 218 cases of grave reduction of vision caused by bilateral malformation of the ocular bulb. Acta Ophthalmol (Copenh). 1968; 46(3):355-60. View

5.
Cuendet J . [Complicated microphthalmia]. Ophthalmologica. 1961; 141:380-5. DOI: 10.1159/000304084. View