Heritable Unilateral Clinical Anophthalmia

Ophthalmic Plastic and Reconstructive Surgery

Volumn 20, Issue 2, 2004, Pages 166-168

  Griepentrog, Gregory J ^a   Lucarelli, Mark J ^a  

^a UNIVERSITY OF WISCONSIN SCHOOL OF MEDICINE AND PUBLIC HEALTH   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ANOPHTHALMIA; ARTICLE; CASE REPORT; COMPUTER ASSISTED TOMOGRAPHY; EYE DISEASE; FEMALE; GENETICS; HUMAN; MALE; NEWBORN; RADIOGRAPHY;

ADULT; ANOPHTHALMOS; EYE DISEASES, HEREDITARY; FEMALE; HUMANS; INFANT, NEWBORN; MALE; TOMOGRAPHY, X-RAY COMPUTED;

EID: 3843080967     PISSN: 07409303     EISSN: 15372677     Source Type: Journal    
DOI: 10.1097/01.IOP.0000117343.59101.AA     Document Type: Article

References (11)

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5. Morlé L, Bozon M, Zech JC, et al. A locus for autosomal dominant colobomatous microphthalmia maps to chromosome 15q12-q15. Am J Hum Genet 2000; 67: 1592-7.
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9. Online Mendelian Inheritance in Man, OMIM. Johns Hopkins University, Baltimore, Maryland. MIM Numbers: Alport Syndrome: autosomal dominant [MIM 104200] last edited 11/6/2000, autosomal recessive [MIM 203780] last edited 3/14/2000, X-linked [MIM 201050] last edited 5/3/2001. Available at:. Accessed on September 2, 2003.
10. Handler LF, Heher KL, Katowitz JA. Management of the microphthalmic orbit. In: Katowitz JA. Pediatric Oculoplastic Surgery. New York: Springer-Verlag; 2002: 559-83.
11. Wiese KG, Vogel M, Guthoff R, et al. Treatment of congenital anophthalmos with self-inflating polymer expanders: a new method. J Craniomaxillofac Surg 1999; 27: 72-6.