Abstract
A 5 day old male with bilateral anophthalmos, hypospadias, bifid scrotum, micrognathia, and cleft palate with normal chromosomes is described. There have been two case reports with similar clinical manifestations but associated with interstitial deletion of 14q (q22q23). We propose that either our patient represents a new syndrome or has a microdeletion which could not be detected on routine cytogenetics. High quality cytogenetics and FISH may show microdeletions in patients presenting with this clinical picture and normal chromosomes.
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- Baraitser M., Winter R. M., Taylor D. S. Lenz microphthalmia--a case report. Clin Genet. 1982 Aug;22(2):99–101. doi: 10.1111/j.1399-0004.1982.tb01420.x. [DOI] [PubMed] [Google Scholar]
- Bennett C. P., Betts D. R., Seller M. J. Deletion 14q (q22q23) associated with anophthalmia, absent pituitary, and other abnormalities. J Med Genet. 1991 Apr;28(4):280–281. doi: 10.1136/jmg.28.4.280. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Elliott J., Maltby E. L., Reynolds B. A case of deletion 14(q22.1-->q22.3) associated with anophthalmia and pituitary abnormalities. J Med Genet. 1993 Mar;30(3):251–252. doi: 10.1136/jmg.30.3.251. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Traboulsi E. I., Lenz W., Gonzales-Ramos M., Siegel J., Macrae W. G., Maumenee I. H. The Lenz microphthalmia syndrome. Am J Ophthalmol. 1988 Jan 15;105(1):40–45. doi: 10.1016/0002-9394(88)90119-5. [DOI] [PubMed] [Google Scholar]