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Arch Pediatr Adolesc Med. 2000;154(5):525-526. doi:.
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Figure 1. The eyes are unusual in appearance because of large pupillary apertures with apparent absence of iris tissue.

Aniridia is a rare condition occurring in 1 in 64,000 to 1 in 96,000 live births.1 Actually, the term is a misnomer since iris tissue is not absent but is hypoplastic. The disorder is not a simple defect of iris tissue; other parts of the eye are affected as well, including the cornea, anterior chamber angle, lens, retina, and optic nerve. The abnormality is apparent at birth in most cases because of the abnormally large pupils, almost always bilaterally, and the presence of nystagmus.

Three genetic forms of aniridia have been described. Familial aniridia, designated AN 1, is an isolated ocular defect accounting for approximately two thirds of all cases and inherited in an autosomal dominant fashion. A microdeletion at band 13 on the short arm of chromosome 11 (11p13) is responsible for AN 1.2,3 Only the aniridia locus is affected; all neighboring genes are spared.4

Sporadic nonfamilial aniridia (AN 2) comprises almost one third of congenital aniridia cases. The genetic defect is also a deletion or mutation of the same chromosome, 11p13, but the defect may also involve the contiguous Wilms tumor suppressor gene (WT 1). One fourth to one third of these patients will develop Wilms tumor, usually by age 3 years.5 The association of aniridia and Wilms tumor is known as Miller syndrome. In contrast to AN 2, only one case of Wilms tumor has been reported in children with AN 1.6

Individuals with Wilms tumor and aniridia may have a more extensive deletion of chromosome 11p13, creating the WAGR contiguous gene syndrome, which includes Wilms tumor, aniridia, genitourinary anomalies, and mental retardation.5 Children with this syndrome have a rather characteristic appearance with a long, narrow face, prominent nose, and low-set, poorly lobulated ears.7 The palpebral fissures are short and downward slanted. Additional abnormalities may include growth failure, microcephaly, delayed closure of the anterior fontanel, and tracheomalacia.8

The third form, AN 3, accounts for approximately 2% of cases of aniridia. Known as Gillespie syndrome, AN 3 is associated with mental retardation, cataracts, and cerebellar ataxia.5 This form of aniridia is an autosomal recessive disorder, with about one third of cases occurring sporadically.

Individuals with aniridia usually have or develop additional ocular and visual problems. Glaucoma develops in up to 75% of cases, usually in the preadolescent or early adult years. Congenital or infantile glaucoma may occur.4,5 Cataracts develop in the first 2 decades of life in 50% to 85% of cases.4 Infants with AN 2 may have cataracts in the neonatal period.5 Superficial corneal opacification with or without vascularization may occur, occasionally resulting in a totally opaque cornea, which may demonstrate relentless progression by age 2 years. Corneal transplantation may be necessary.9

Macular and optic nerve hypoplasia is common, resulting in poor vision and troublesome photophobia. Narrowed palpebral fissures with brow furrowing are characteristic, attributed to the voluntary grimace resulting from photophobia.4 A visual acuity of 20/100 or worse in the better eye is found in 86% of patients.7 Macular involvement produces nystagmus, which is almost always present. Retinal function approaches normal in some patients.10

Infants with aniridia must be followed up closely to detect the development of glaucoma and other ocular complications to preserve as much sight as possible. Children with AN 2 must undergo regularly scheduled renal ultrasonography to detect the development of Wilms tumors.

Accepted for publication October 6, 1999.

Reprints: Richard W. Hartmann, Jr, MD, Halifax Medical Center, 303 N Clyde Morris Blvd, Daytona Beach, FL 32114-2732.

Nelson  LB Disorders of the eye. Behrman  REKliegman  RMArvin  AMeds.Nelson Textbook of Pediatrics. 15th ed. Philadelphia, Pa WB Saunders Co1996;1764- 1803
Ferrell  REChakravarti  AHittner  HMRiccardi  VM Autosomal dominant aniridia: probable linkage to acid phosphatase-1 locus on chromosome 2. Proc Natl Acad Sci U S A. 1980;771580- 1582
Lyons  LAMartha  AMintz-Hittner  HASaunders  GFFerrell  RE Resolution of the two loci for autosomal dominant aniridia, AN 1 and AN2, to a single locus on chromosome 11p13. Genomics. 1992;13925- 930
Ivanov  IShuper  AShohat  MSnir  MWeitz  R Aniridia: recent achievements in paediatric practice. Eur J Pediatr. 1995;154795- 800
Eagle  RC  Jr Congenital, developmental, and degenerative disorders of the iris and ciliary body. Albert  DMJakobiec  FAeds.Principles and Practice of Ophthalmology: Clinical Practice. Vol 1. Philadelphia, Pa WB Saunders Co1994;367- 389
Mets  MBCross  HE Aniridia. Buyse  MLed.Birth Defect Encyclopedia. Dover, Mass Center for Birth Defects Information Services1990;144- 145
Nelson  LBSpaeth  GLNowinski  TSMargo  CEJackson  L Aniridia: a review. Surv Ophthalmol. 1984;28621- 642
Jotterand  VBoisjoly  HMHarnois  C  et al.  11p13 Deletion, Wilms tumour, and aniridia: unusual genetic, non-ocular and ocular features of three cases. Br J Ophthalmol. 1990;74568- 570
Nishida  KKinoshita  SOhashi  YKuwayama  YYamamoto  S Ocular surface abnormalities in aniridia. Am J Ophthalmol. 1995;120368- 375
Tremblay  FGupta  SKDeBecker  IGuernsey  DLNeumann  PE Effects of PAX6 mutations on retinal function: an electroretinographic study. Am J Ophthalmol. 1998;126211- 218

Tables

References

Nelson  LB Disorders of the eye. Behrman  REKliegman  RMArvin  AMeds.Nelson Textbook of Pediatrics. 15th ed. Philadelphia, Pa WB Saunders Co1996;1764- 1803
Ferrell  REChakravarti  AHittner  HMRiccardi  VM Autosomal dominant aniridia: probable linkage to acid phosphatase-1 locus on chromosome 2. Proc Natl Acad Sci U S A. 1980;771580- 1582
Lyons  LAMartha  AMintz-Hittner  HASaunders  GFFerrell  RE Resolution of the two loci for autosomal dominant aniridia, AN 1 and AN2, to a single locus on chromosome 11p13. Genomics. 1992;13925- 930
Ivanov  IShuper  AShohat  MSnir  MWeitz  R Aniridia: recent achievements in paediatric practice. Eur J Pediatr. 1995;154795- 800
Eagle  RC  Jr Congenital, developmental, and degenerative disorders of the iris and ciliary body. Albert  DMJakobiec  FAeds.Principles and Practice of Ophthalmology: Clinical Practice. Vol 1. Philadelphia, Pa WB Saunders Co1994;367- 389
Mets  MBCross  HE Aniridia. Buyse  MLed.Birth Defect Encyclopedia. Dover, Mass Center for Birth Defects Information Services1990;144- 145
Nelson  LBSpaeth  GLNowinski  TSMargo  CEJackson  L Aniridia: a review. Surv Ophthalmol. 1984;28621- 642
Jotterand  VBoisjoly  HMHarnois  C  et al.  11p13 Deletion, Wilms tumour, and aniridia: unusual genetic, non-ocular and ocular features of three cases. Br J Ophthalmol. 1990;74568- 570
Nishida  KKinoshita  SOhashi  YKuwayama  YYamamoto  S Ocular surface abnormalities in aniridia. Am J Ophthalmol. 1995;120368- 375
Tremblay  FGupta  SKDeBecker  IGuernsey  DLNeumann  PE Effects of PAX6 mutations on retinal function: an electroretinographic study. Am J Ophthalmol. 1998;126211- 218

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