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Faivre L, Masurel-Paulet A, Collod-Béroud G, Callewaert BL, Child AH, Stheneur C, Binquet C, Gautier E, Chevallier B, Huet F, Loeys BL, Arbustini E, Mayer K,Arslan-Kirchner M, Kiotsekoglou A, Comeglio P, Grasso M, Halliday DJ, Béroud C, Bonithon-Kopp C, Claustres M, Robinson PN, Adès L, De Backer J, Coucke P, Francke U, De Paepe A, Boileau C, Jondeau G. Clinical and molecular study of 320 children with Marfan syndrome and related type I fibrillinopathies in a series of 1009 probands with pathogenic FBN1 mutations. Pediatrics 123:391-8, 2009.

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Article

Isolated Dislocation of Ocular Lens

1Department of Pediatrics and Neonatology, Castelli Hospital, Verbania, Italy

2Department of Obstetrics and Gynecology, Castelli Hospital, Verbania, Italy

3University of Eastern Piedmont, Novara, Italy


American Journal of Medical Case Reports. 2016, Vol. 4 No. 3, 97-100
DOI: 10.12691/ajmcr-4-3-7
Copyright © 2016 Science and Education Publishing

Cite this paper:
Gabriela Acucella, Enrico Finale, Gaetano Auletta, Andrea Guala. Isolated Dislocation of Ocular Lens. American Journal of Medical Case Reports. 2016; 4(3):97-100. doi: 10.12691/ajmcr-4-3-7.

Correspondence to: Enrico  Finale, Department of Obstetrics and Gynecology, Castelli Hospital, Verbania, Italy. Email: enrico.finale@gmail.com

Abstract

We describe a case of a child whit isolated dislocated of ocular lens, due to mutation in FBN1 gene. Differential syndromic diagnosis is made and we discuss to importance of clinical follow-up to exclude/confirm cardiologic complications due to Marfan syndrome.

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