Literature DB >> 1344755

Congenital Marfan syndrome with contractures. A clinicopathological report.

F M Meire1, J Van Egmond, M Hanssens.   

Abstract

Children with CMC present with blue sclerae, megalocornea, hypoplastic and translucent irides, miosis and high myopia. The lenses may be dislocated as in familial Marfan syndrome but they are often in place and microspherophakic. The clinical history of a boy with CMC is presented. Pathological examination of the eyes showed megalophthalmos with thinned sclera, anomalies of the chamber angle and iris, ill-developed ciliary body and choroid and a small in situ lens.

Entities:  

Mesh:

Year:  1992        PMID: 1344755

Source DB:  PubMed          Journal:  Bull Soc Belge Ophtalmol        ISSN: 0081-0746


  3 in total

1.  Megalocornea. Clinical and genetic aspects.

Authors:  F M Meire
Journal:  Doc Ophthalmol       Date:  1994       Impact factor: 2.379

2.  LTBP2 null mutations in an autosomal recessive ocular syndrome with megalocornea, spherophakia, and secondary glaucoma.

Authors:  Julie Désir; Yves Sznajer; Fanny Depasse; Françoise Roulez; Marc Schrooyen; Françoise Meire; Marc Abramowicz
Journal:  Eur J Hum Genet       Date:  2010-02-24       Impact factor: 4.246

3.  Rhegmatogenous retinal detachment with a giant tear located in the intermediate periphery: Two case reports.

Authors:  Ryohsuke Kohmoto; Masanori Fukumoto; Takaki Sato; Shou Oosuka; Takatoshi Kobayashi; Teruyo Kida; Hiroyuki Suzuki; Tsunehiko Ikeda
Journal:  Medicine (Baltimore)       Date:  2019-01       Impact factor: 1.817

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.