» Articles » PMID: 9222975

A Case of Lenz Microphthalmia Syndrome

Overview
Journal J Med Genet
Specialty Genetics
Date 1997 Jul 1
PMID 9222975
Citations 3
Authors
Affiliations
Soon will be listed here.
Abstract

Lenz microphthalmia syndrome was first described by Lenz et al in 1955. The cardinal features of the syndrome are microphthalmia or anophthalmos, narrow shoulders, other skeletal anomalies, and dental and urogenital malformations. Here we present a case of Lenz microphthalmia syndrome who shows the typical characteristics and, additionally, dysgenesis of the corpus callosum associated with dilatation of the lateral ventricles. The patient, a 13 year old male, was referred to our hospital by a dental hospital for genetic counselling. On physical examination, height, weight, and head circumference were below the 3rd centile and he had brachymicrocephaly, a preauricular tag, microphthalmia, missing teeth, narrow shoulders, long, proximally placed thumbs, hypospadias, cryptorchidism, and a normal IQ. Ophthalmological examination showed microcornea, sclerocornea, absence of the pupil, no vision in the left eye and decreased vision and a small pupil in the right eye in addition to his bilateral microphthalmia. Cranial MRI showed dilatation of the lateral ventricles and dysgenesis of the corpus callosum.

Citing Articles

Lenz microphthalmia syndrome in neurosurgical practice: a case report and review of the literature.

Monticelli M, De Marco R, Garbossa D Childs Nerv Syst. 2021; 37(8):2713-2718.

PMID: 33491151 PMC: 8342332. DOI: 10.1007/s00381-020-05035-1.


A rare case of the lenz syndrome.

T S, K K, M S R, K N, M P J Clin Diagn Res. 2013; 7(2):347-9.

PMID: 23543842 PMC: 3592308. DOI: 10.7860/JCDR/2013/5009.2764.


BCOR analysis in patients with OFCD and Lenz microphthalmia syndromes, mental retardation with ocular anomalies, and cardiac laterality defects.

Hilton E, Johnston J, Whalen S, Okamoto N, Hatsukawa Y, Nishio J Eur J Hum Genet. 2009; 17(10):1325-35.

PMID: 19367324 PMC: 2826145. DOI: 10.1038/ejhg.2009.52.

References
1.
Pena S, Shokeir M . Autosomal recessive cerebro-oculo-facio-skeletal (COFS) syndrome. Clin Genet. 1974; 5(4):285-93. DOI: 10.1111/j.1399-0004.1974.tb01695.x. View

2.
Hopkins I, Humphrey I, Keith C, Susman M, Webb G, TURNER E . The Aicardi syndrome in a 47, XXY male. Aust Paediatr J. 1979; 15(4):278-80. DOI: 10.1111/j.1440-1754.1979.tb01246.x. View

3.
Glanz A, Forse A, Polomeno R, Cole D . Lenz microphthalmia: a malformation syndrome with variable expression of multiple congenital anomalies. Can J Ophthalmol. 1983; 18(1):41-4. View

4.
Jeret J, Serur D, Wisniewski K, Lubin R . Clinicopathological findings associated with agenesis of the corpus callosum. Brain Dev. 1987; 9(3):255-64. DOI: 10.1016/s0387-7604(87)80042-6. View

5.
Traboulsi E, Lenz W, Siegel J, Macrae W, Maumenee I . The Lenz microphthalmia syndrome. Am J Ophthalmol. 1988; 105(1):40-5. DOI: 10.1016/0002-9394(88)90119-5. View