Unilateral persistent fetal vasculature coexisting with anterior segment dysgenesis
Author:
Publisher
Springer Science and Business Media LLC
Subject
Ophthalmology
Link
http://link.springer.com/content/pdf/10.1007/s10792-013-9757-z.pdf
Reference5 articles.
1. Cerón O, Lou PL, Kroll AJ et al (2008) The vitreo-retinal manifestations of persistent hyperplasic primary vitreous (PHPV) and their management. Int Ophthalmol Clin 48:53–62 (Review)
2. Khokhar S, Tejwani LK, Kumar G et al (2011) Approach to cataract with persistent hyperplastic primary vitreous. J Cataract Refract Surg 37:1382–1385
3. Yamada K, Ozeki H, Ieda M et al (1997) Four cases of persistent hyperplastic primary vitreous. Nihon Ganka Gakkai Zasshi 101:826–831 (Japanese)
4. Suzuki K, Nakamura M, Amano E et al (2006) Case of chromosome 6p25 terminal deletion associated with Axenfeld–Rieger syndrome and persistent hyperplastic primary vitreous. Am J Med Genet A 140:503–508
5. Kelberman D, Islam L (2011) Hold. Digenic inheritance of mutations in FOXC1 and PITX2: correlating transcription factor function and Axenfeld–Rieger disease severity. Hum Mutat 32:1144–1152
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