On the nosology of the "primary true microcephaly, chorioretinal dysplasia, lymphoedema" association
- PMID: 8556819
- DOI: 10.1111/j.1399-0004.1995.tb04072.x
On the nosology of the "primary true microcephaly, chorioretinal dysplasia, lymphoedema" association
Abstract
We describe a male child with prenatal growth retardation, true microcephaly, pedal lymphoedema and characteristic ocular anomalies. Ophthalmological examination revealed remnants of the posterior hyaloidea, more pronounced in the right eye where a retinal fold extended from the papilla into the vitreum, chorioretinal dysplasia with narrow retinal vessels, multiple large round areas of chorioretinal atrophy and atrophic papillae. The associations "Microcephaly-chorioretinal dysplasia", "Microcephaly-retinal folds" and "Microcephaly-lymphoedema" have been reported as separate autosomal dominant conditions. The findings in the present child suggest that these associations could be variable expressions of the same autosomal dominant condition.
Similar articles
-
[Ophthalmological findings in microcephaly-lymphoedema-chorioretinal dysplasia syndrome].Klin Monbl Augenheilkd. 2009 Apr;226(4):344-6. doi: 10.1055/s-0028-1109313. Epub 2009 Apr 21. Klin Monbl Augenheilkd. 2009. PMID: 19384796 German.
-
Microcephaly, lymphedema, and chorioretinal dysplasia: report of two additional cases.Am J Med Genet. 1994 Nov 1;53(2):99-101. doi: 10.1002/ajmg.1320530202. Am J Med Genet. 1994. PMID: 7856652
-
Autosomal dominant microcephaly--lymphoedema-chorioretinal dysplasia syndrome.Br J Ophthalmol. 2001 Apr;85(4):499-500. doi: 10.1136/bjo.85.4.496d. Br J Ophthalmol. 2001. PMID: 11302131 Free PMC article. No abstract available.
-
Microcephaly, lymphedema, chorioretinal dysplasia (MLCRD) syndrome.J Pediatr Health Care. 2012 Jul-Aug;26(4):306-11. doi: 10.1016/j.pedhc.2011.08.002. Epub 2011 Oct 8. J Pediatr Health Care. 2012. PMID: 22726716 Review. No abstract available.
-
Microcephaly with chorioretinal dysplasia: two case reports and a review of the literature.Ophthalmic Genet. 2009 Dec;30(4):157-60. doi: 10.3109/13816810903147980. Ophthalmic Genet. 2009. PMID: 19852571 Review.
Cited by
-
Congenital focal abnormalities of the retina and retinal pigment epithelium.Eye (Lond). 2020 Nov;34(11):1973-1988. doi: 10.1038/s41433-020-0902-4. Epub 2020 May 4. Eye (Lond). 2020. PMID: 32367006 Free PMC article. Review.
-
Congenital microcephaly and chorioretinopathy due to de novo heterozygous KIF11 mutations: five novel mutations and review of the literature.Am J Med Genet A. 2014 Nov;164A(11):2879-86. doi: 10.1002/ajmg.a.36707. Epub 2014 Aug 12. Am J Med Genet A. 2014. PMID: 25115524 Free PMC article. Review.
-
No evidence of locus heterogeneity in familial microcephaly with or without chorioretinopathy, lymphedema, or mental retardation syndrome.Orphanet J Rare Dis. 2015 May 2;10:52. doi: 10.1186/s13023-015-0271-4. Orphanet J Rare Dis. 2015. PMID: 25934493 Free PMC article.
-
The mitotic spindle: linking teratogenic effects of Zika virus with human genetics?Mol Cytogenet. 2016 Apr 19;9:32. doi: 10.1186/s13039-016-0240-1. eCollection 2016. Mol Cytogenet. 2016. PMID: 27099632 Free PMC article.
-
Genotype Phenotype Correlation and Variability in Microcephaly Associated With Chorioretinopathy or Familial Exudative Vitreoretinopathy.Invest Ophthalmol Vis Sci. 2020 Nov 2;61(13):2. doi: 10.1167/iovs.61.13.2. Invest Ophthalmol Vis Sci. 2020. PMID: 33137195 Free PMC article.
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Medical
Molecular Biology Databases