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Pericentric syndrome (pericentric inversion of chromosome 11)


Pericentric Syndrome (pericentric Inversion of Chromosome 11)

General: Etiology unknown; leukocyte chromosomes show a pericentric inversion of c 313e41d hromosome 11.

Ocular: Strabismus; hypertelorism; congenital glaucoma; aniridia; corneal disease; epicanthic folds.

Clinical: Microcephaly; broad nasal bridge; arched palate; hyperextensibility of elbows; left hand shows single transverse crease, and right hand shows three palmar creases radiating from radial border.



Broughton WL, et al. Congenital glaucoma and other ocular abnormalities associated with pericentric inversion of chromosome 11. Arch Ophthalmol 1983; 101:594-597.

Pergament E. The pericentric syndrome. Lancet 1967; 2:777.




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