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Page 1
Microspherophakia.
Chan RT, Collin HB. Chan RT, et al. Clin Exp Optom. 2002 Sep;85(5):294-9. doi: 10.1111/j.1444-0938.2002.tb03085.x. Clin Exp Optom. 2002. PMID: 12366350 Free article. Review.
Microspherophakia is present when the crystalline lens is small and relatively spherical with increased antero-posterior thickness. Clinical findings for a patient with idiopathic bilateral microspherophakia are described. The patient was moderately myopic with slig …
Microspherophakia is present when the crystalline lens is small and relatively spherical with increased antero-posterior thickness. C …
A systematic approach to the management of microspherophakia.
Venkataraman P, Haripriya A, Mohan N, Rajendran A. Venkataraman P, et al. Indian J Ophthalmol. 2022 Jul;70(7):2262-2271. doi: 10.4103/ijo.IJO_2888_21. Indian J Ophthalmol. 2022. PMID: 35791105 Free PMC article. Review.
Microspherophakia is a rare developmental abnormality of the crystalline lens with a myriad of ocular and systemic associations. ...
Microspherophakia is a rare developmental abnormality of the crystalline lens with a myriad of ocular and systemic associations. ...
Weill-Marchesani syndrome with advanced glaucoma and corneal endothelial dysfunction: a case report and literature review.
Guo H, Wu X, Cai K, Qiao Z. Guo H, et al. BMC Ophthalmol. 2015 Jan 9;15:3. doi: 10.1186/1471-2415-15-3. BMC Ophthalmol. 2015. PMID: 25571963 Free PMC article. Review.
CONCLUSIONS: Weill-Marchesani syndrome could be diagnosed by microspherophakia, high myopia, secondary glaucoma, and systemic abnormalities such as brachymorphia and brachydactyly. Removal of the microspherophakia is recommended to control intraocular pressure and i …
CONCLUSIONS: Weill-Marchesani syndrome could be diagnosed by microspherophakia, high myopia, secondary glaucoma, and systemic abnorma …
Clinical homogeneity and genetic heterogeneity in Weill-Marchesani syndrome.
Faivre L, Dollfus H, Lyonnet S, Alembik Y, Mégarbané A, Samples J, Gorlin RJ, Alswaid A, Feingold J, Le Merrer M, Munnich A, Cormier-Daire V. Faivre L, et al. Am J Med Genet A. 2003 Dec 1;123A(2):204-7. doi: 10.1002/ajmg.a.20289. Am J Med Genet A. 2003. PMID: 14598350 Review.
Weill-Marchesani syndrome (WMS) is a rare condition characterized by short stature, brachydactyly, joint stiffness, and characteristic eye abnormalities including microspherophakia, ectopia of lens, severe myopia, and glaucoma. Both autosomal recessive (AR) and autosomal d …
Weill-Marchesani syndrome (WMS) is a rare condition characterized by short stature, brachydactyly, joint stiffness, and characteristic eye a …
From tall to short: the role of TGFβ signaling in growth and its disorders.
Le Goff C, Cormier-Daire V. Le Goff C, et al. Am J Med Genet C Semin Med Genet. 2012 Aug 15;160C(3):145-53. doi: 10.1002/ajmg.c.31337. Epub 2012 Jul 12. Am J Med Genet C Semin Med Genet. 2012. PMID: 22791552 Review.
WMS is characterized by the presence of dislocation of microspherophakia and has autosomal dominant or recessive mode of inheritance. ...
WMS is characterized by the presence of dislocation of microspherophakia and has autosomal dominant or recessive mode of inheritance. …
Weill-Marchesani Syndrome, a Rare Presentation of Severe Short Stature with Review of the Literature.
Al Motawa MNA, Al Shehri MSS, Al Buali MJ, Al Agnam AAM. Al Motawa MNA, et al. Am J Case Rep. 2021 May 31;22:e930824. doi: 10.12659/AJCR.930824. Am J Case Rep. 2021. PMID: 34057920 Free PMC article. Review.
It is characterized by short stature, brachydactyly, joint stiffness, ocular abnormalities, mainly microspherophakia and glaucoma, and occasionally cardiac defects. CASE REPORT A 9-year-old boy had bilateral narrow-angle glaucoma with lens subluxation, elevated intraocular …
It is characterized by short stature, brachydactyly, joint stiffness, ocular abnormalities, mainly microspherophakia and glaucoma, an …