Anophthalmos

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Anophthalmos

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Anophthalmia can be challenging to treat. Patients with anophthalmia often require a team of specialists for proper care. Considerations include identifying associated abnormalities (eg, microcephalia) that may present additional risks to the patient. Aesthetics and cosmesis are important to the self-esteem of the patient. Oculofacial surgery may be costly and may be beyond the reach of many families. Long-term follow-up of the patient is necessary for maximizing his or her function and self-esteem.

True or primary anophthalmos is very rare. Only when there is a complete absence of the ocular tissue within the orbit can a diagnosis of true anophthalmos be made. Extreme microphthalmos is seen more commonly. In this condition, a very small globe is present within the orbital soft tissue, which is not visible on initial examination.

Anophthalmia and microphthalmia may occur secondary to the arrest of development of the eye at various stages of growth of the optic vesicle. It is important to recognize microphthalmia because the development of the orbital region, as well as the lids and the fornices, is dependent on the presence of a normal-sized eye in utero.

Anophthalmia may lead to serious problems in a child due to not only the absence of a seeing eye but also the secondary disfigurement of the orbit, the lids, and the eye socket. Early treatment with various expanders or surgery, when necessary, will help decrease the orbital asymmetry and cosmetic deformities in these children.

See the clinical images below:

Anophthalmia occurs when the neuroectoderm of the primary optic vesicle fails to develop properly from the anterior neural plate of the neural tube during embryological development. The more commonly seen microphthalmia can result from a problem in development of the globe at any stage of growth of the optic vesicle.

The most common genetic disturbance associated with anophthalmia and microphthalmia is de novo loss of function mutations in the SOX2 gene. [1] In consanguineous families, the gene ALDH1A3 may also play an important role. [2]

Proper growth of the orbital region is dependent on the presence of an eye, which stimulates growth of the orbit and proper formation of the lids and the ocular fornices. Commonly, a child born with anophthalmia has a small orbit with narrow palpebral fissure and shrunken fornices.

United States

Congenital anophthalmos is a very rare condition that has a reported prevalence rate of 0.18 per 10,000 births. [3]

International

European rates are similar to those seen in the United States and have been reported as 0.19 case per 10,000 births. [4]

Australian rates are reported as 0.06-0.42 case per 10,000 births and 0.2-1.7 cases per 10,000 births for anophthalmia and microphthalmia, respectively. [5]

Growth and development of the bony orbit is directly dependent on outgrowth of the globe.

Lack of an eye or a microphthalmic eye causes improper development of the orbit.

A small bony orbit results in hemifacial hypoplasia and will not allow a prosthesis to be fit. The cosmetic deformity can be quite significant.

Classically, racial predilection for anophthalmos has not been reported; however, recent studies have shown an elevated prevalence in some ethnic groups. These groups include Pakistani and Scottish children. Genetic, environmental, and possible classification issues may explain these high rates of disease and need to be explored further. [6]

Sexual predilection for congenital anophthalmos has not been reported.

Anophthalmos occurs in utero and is a congenital anomaly that is present at birth.

Mauri L, Franzoni A, Scarcello M, Sala S, Garavelli L, Modugno A, et al. SOX2, OTX2 and PAX6 analysis in subjects with anophthalmia and microphthalmia. Eur J Med Genet. 2015 Feb. 58 (2):66-70. [Medline].

Abouzeid H, Favez T, Schmid A, Agosti C, Youssef M, Marzouk I, et al. Mutations in ALDH1A3 represent a frequent cause of microphthalmia/anophthalmia in consanguineous families. Hum Mutat. 2014 Aug. 35 (8):949-53. [Medline].

Shaw GM, Carmichael SL, Yang W, Harris JA, Finnell RH, Lammer EJ. Epidemiologic characteristics of anophthalmia and bilateral microphthalmia among 2.5 million births in California, 1989-1997. Am J Med Genet A. 2005 Aug 15. 137(1):36-40. [Medline].

Boyd PA, Haeusler M, Barisic I. EUROCAT Report 9: Surveillance of congenital anomalies in Europe 1980-2008. Birth Defects Res A Clin Mol Teratol. 2011 Mar. 91 Suppl 1:S1. [Medline].

Skalicky SE, White AJ, Grigg JR, et al. Microphthalmia, anophthalmia, and coloboma and associated ocular and systemic features: understanding the spectrum. JAMA Ophthalmol. 2013 Dec. 131(12):1517-24. [Medline].

Shah SP, Taylor AE, Sowden JC, Ragge NK, Russell-Eggitt I, Rahi JS. Anophthalmos, microphthalmos, and typical coloboma in the United Kingdom: a prospective study of incidence and risk. Invest Ophthalmol Vis Sci. 2011 Jan. 52(1):558-64. [Medline].

Roy FH, ed. Ocular Differential Diagnosis. 6th ed. Baltimore, MD: Lippincott, Williams & Wilkins; 1997. 263.

Kennedy RE. The effect of early enucleation on the orbit; in animals and humans. Am J Ophthalmol. 1965 Aug. 60:277-306. [Medline].

Putterman AM. Ocular socket problems. Waltman SR, Keates RH, Hoyt CS, eds. Surgery of the Eye. New York: Churchill Livingston; 1988. 749-758.

Macchiaroli A, Kelberman D, Auriemma RS, et al. A novel heterozygous SOX2 mutation causing congenital bilateral anophthalmia, hypogonadotropic hypogonadism and growth hormone deficiency. Gene. 2014 Jan 25. 534(2):282-5. [Medline].

Ahmad ME, Dada R, Dada T, Kucheria K. 14q(22) deletion in a familial case of anophthalmia with polydactyly. Am J Med Genet A. 2003 Jul 1. 120(1):117-22. [Medline].

Hoover-Fong JE, Cai J, Cargile CB, Thomas GH, Patel A, Griffin CA. Facial dysgenesis: a novel facial syndrome with chromosome 7 deletion p15.1-21.1. Am J Med Genet A. 2003 Feb 15. 117A(1):47-56. [Medline].

Bakrania P, Robinson DO, Bunyan DJ, et al. SOX2 anophthalmia syndrome: 12 new cases demonstrating broader phenotype and high frequency of large gene deletions. Br J Ophthalmol. 2007 Nov. 91(11):1471-6. [Medline].

Bardakjian TM, Schneider A. The genetics of anophthalmia and microphthalmia. Curr Opin Ophthalmol. 2011 Sep. 22(5):309-13. [Medline].

Yahyavi M, Abouzeid H, Gawdat G, et al. ALDH1A3 loss of function causes bilateral anophthalmia/microphthalmia and hypoplasia of the optic nerve and optic chiasm. Hum Mol Genet. 2013 Aug 15. 22(16):3250-8. [Medline]. [Full Text].

Albernaz VS, Castillo M, Hudgins PA, Mukherji SK. Imaging findings in patients with clinical anophthalmos. AJNR Am J Neuroradiol. 1997 Mar. 18(3):555-61. [Medline].

Marchac D, Cophignon J, Achard E, Dufourmentel C. Orbital expansion for anophthalmia and micro-orbitism. Plast Reconstr Surg. 1977 Apr. 59(4):486-91. [Medline].

Mustarde JE. The orbital rim. Mustarde JC, Jancsous IT, eds. Plastic Surgery in Infancy and Children. Edinburgh: Churchill Livingston; 1988. 150-155.

Tucker SM, Sapp N, Collin R. Orbital expansion of the congenitally anophthalmic socket. Br J Ophthalmol. 1995 Jul. 79(7):667-71. [Medline].

Krastinova D, Kelly MB, Mihaylova M. Surgical management of the anophthalmic orbit, part 1: congenital. Plast Reconstr Surg. 2001 Sep 15. 108(4):817-26. [Medline].

Quaranta-Leoni FM. Treatment of the anophthalmic socket. Curr Opin Ophthalmol. 2008 Sep. 19(5):422-7. [Medline].

Gundlach KK, Guthoff RF, Hingst VH, Schittkowski MP, Bier UC. Expansion of the socket and orbit for congenital clinical anophthalmia. Plast Reconstr Surg. 2005 Oct. 116(5):1214-22. [Medline].

Cepela MA, Nunery WR, Martin RT. Stimulation of orbital growth by the use of expandable implants in the anophthalmic cat orbit. Ophthal Plast Reconstr Surg. 1992. 8(3):157-67; discussion 168-9. [Medline].

Tse DT, Pinchuk L, Davis S, Falcone SF, Lee W, Acosta AC, et al. Evaluation of an integrated orbital tissue expander in an anophthalmic feline model. Am J Ophthalmol. 2007 Feb. 143(2):317-327. [Medline].

Tse DT, Abdulhafez M, Orozco MA, Tse JD, Azab AO, Pinchuk L. Evaluation of an integrated orbital tissue expander in congenital anophthalmos: report of preliminary clinical experience. Am J Ophthalmol. 2011 Mar. 151(3):470-82.e1. [Medline].

Quaranta-Leoni FM. Congenital anophthalmia: current concepts in management. Curr Opin Ophthalmol. 2011 Sep. 22(5):380-4. [Medline].

Mazzoli RA, Raymond WR 4th, Ainbinder DJ, Hansen EA. Use of self-expanding, hydrophilic osmotic expanders (hydrogel) in the reconstruction of congenital clinical anophthalmos. Curr Opin Ophthalmol. 2004 Oct. 15(5):426-31. [Medline].

Kotlus BS, Dryden RM. Correction of anophthalmic enophthalmos with injectable calcium hydroxylapatite (Radiesse). Ophthal Plast Reconstr Surg. 2007 Jul-Aug. 23(4):313-4. [Medline].

Tvrdek M, Kozák J. Reconstruction of eyelids with Washio flap in anophthalmia. Acta Chir Plast. 2014. 56 (1-2):20-2. [Medline].

Koh V, Chiam N, Sundar G. Survey of common practices among oculofacial surgeons in the Asia-Pacific region: evisceration, enucleation and management of anophthalmic sockets. Orbit. 2014 Dec. 33 (6):477. [Medline].

Andreotti AM, Goiato MC, Pellizzer EP, Pesqueira AA, Guiotti AM, Gennari-Filho H, et al. Phantom eye syndrome: a review of the literature. ScientificWorldJournal. 2014. 2014:686493. [Medline].

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Nick Mamalis, MD Professor of Ophthalmology, Director of Ocular Pathology, Department of Ophthalmology, John Moran Eye Center, University of Utah School of Medicine; Director, Intermountain Ocular Research Center

Nick Mamalis, MD is a member of the following medical societies: American Academy of Ophthalmology, American Medical Association, American Society of Cataract and Refractive Surgery

Disclosure: Serve(d) as a director, officer, partner, employee, advisor, consultant or trustee for: Anew Optics Inc; Medennium Inc<br/>Received research grant from: ARC Laser Corp; Aaren Scientific Inc; Abbott Medical Optics; Alcon Labs Inc; Allergan; Anew Optics Inc; Bausch & Lomb; Calhoun Vision Inc; ClarVista; Genisphere; HOYA; LensGen; Medennium Inc; Mynosys; Nu-Vue Technologies; Omega; PowerVision; Sharklet.

Scott C Cole, MD, MS Pre-Residency Fellow in Ophthalmic Pathology, Moran Eye Center, University of Utah School of Medicine

Scott C Cole, MD, MS is a member of the following medical societies: American Academy of Ophthalmology, American College of Sports Medicine, American Medical Association

Disclosure: Nothing to disclose.

He Jack Li Research Fellow in Ophthalmic Pathology, John A Moran Eye Center, University of Utah School of Medicine

Disclosure: Nothing to disclose.

Simon K Law, MD, PharmD Clinical Professor of Health Sciences, Department of Ophthalmology, Jules Stein Eye Institute, University of California, Los Angeles, David Geffen School of Medicine

Simon K Law, MD, PharmD is a member of the following medical societies: American Academy of Ophthalmology, Association for Research in Vision and Ophthalmology, American Glaucoma Society

Disclosure: Nothing to disclose.

Hampton Roy, Sr, MD Associate Clinical Professor, Department of Ophthalmology, University of Arkansas for Medical Sciences

Hampton Roy, Sr, MD is a member of the following medical societies: American Academy of Ophthalmology, American College of Surgeons, Pan-American Association of Ophthalmology

Disclosure: Nothing to disclose.

Ron W Pelton, MD, PhD Private Practice, Colorado Springs, Colorado

Ron W Pelton, MD, PhD is a member of the following medical societies: American Academy of Ophthalmology, American College of Surgeons, AO Foundation, American Society of Ophthalmic Plastic and Reconstructive Surgery, Colorado Medical Society

Disclosure: Nothing to disclose.

Andrew James Ollerton, MD Pre-residency Fellow, Ocular Pathology, Moran Eye Center, University of Utah

Andrew James Ollerton, MD is a member of the following medical societies: American Society of Cataract and Refractive Surgery

Disclosure: Nothing to disclose.

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