[1] |
Reese AB. Persistent hyperplastic primary vitreous[J]. Am J Ophthalmol, 1955, 40(3): 317-331.
|
[2] |
Goldberg MF. Persistent fetal vasculature (PFV): an integrated interpretation of signs and symptoms associated with persistent hyperplastic primary vitreous (PHPV)[J]. Am J Ophthalmol, 1997, 124(5): 587-626.
|
[3] |
Solebo AL, Russell-Eggitt I, Cumberland P, et al. Congenital cataract associated with persistent fetal vasculature: findings from IoLunder2[J]. Eye (Lond), 2016, 30(9): 1204-1209.
|
[4] |
Li Y, Li Z, Quan Y, et al. Macrophage recruitment in immune-privileged lens during capsule repair, necrotic fiber removal, and fibrosis[J]. iScience, 2021, 24(6): 102533.
|
[5] |
Son AI, Sheleg M, Cooper MA, et al. Formation of persistent hyperplastic primary vitreous in ephrin-A5-/- mice[J]. Invest Ophthalmol Vis Sci, 2014, 55(3): 1594-1606.
|
[6] |
Arima M, Yoshida S, Nakama T, et al. Involvement of periostin in regression of hyaloidvascular system during ocular development[J]. Invest Ophthalmol Vis Sci, 2012, 53(10): 6495-6503.
|
[7] |
Thornton JD, Swanson DJ, Mary MN, et al. Persistent hyperplastic primary vitreous due to somatic mosaic deletion of the arf tumor suppressor[J]. Invest Ophthalmol Vis Sci, 2007, 48(2): 491-499.
|
[8] |
Lobov IB, Rao S, Carroll TJ, et al. WNT7b mediates macro-phage-induced programmed cell death in patterning of the vasculature[J]. Nature, 2005, 437(7057): 417-421.
|
[9] |
Wang Z, Liu CH, Huang S, et al. Assessment and characterization of hyaloid vessels in mice[J]. J Vis Exp, 2019, PMID: 31157789.
|
[10] |
Rutland CS, Mitchell CA, Nasir M, et al. Microphthalmia, persistent hyperplastic hyaloid vasculature and lens anomalies following overexpression of VEGF-A188 from the alphaA-crystallin promoter[J]. Mol Vis, 2007, 13: 47-56.
|
[11] |
Hahn P, Lindsten T, Tolentino M, et al. Persistent fetal ocular vasculature in mice deficient in bax and bak[J]. Arch Ophthalmol, 2005, 123(6): 797-802.
|
[12] |
Zigler JS, Valapala M, Shang P, et al. βA3/A1-crystallin and persistent fetal vasculature (PFV) disease of the eye[J]. Biochim Biophys Acta, 2016, 1860(1): 287-298.
|
[13] |
Maqsood H, Younus S, Fatima M, et al. Bilateral persistent hyperplastic primary vitreous: a case report and review of the literature[J]. Cureus, 2021, 13(2): e13105.
|
[14] |
Al-Moujahed A, Callaway NF, Ludwig CA, et al. Morning glory optic nerve in Aicardi syndrome: Report of a case with fluorescein angiography[J]. Eur J Ophthalmol, 2021, 31(6): NP61-NP64.
|
[15] |
Shastry BS. Persistent hyperplastic primary vitreous: congenital malformation of the eye[J]. Clin Exp Ophthalmol, 2009, 37(9): 884-890.
|
[16] |
Pollard ZF. Persistent hyperplastic primary vitreous: diagnosis, treatment and results[J]. Trans Am Ophthalmol Soc, 1997, 95: 487-549.
|
[17] |
Yeh CT, Chen KJ, Liu L, et al. Visual and anatomical outcomes with vitrectomy in posterior or combined persistent fetal vasculature in an Asian population[J]. Ophthalmic Surg Lasers Imaging Retina, 2019, 50(6): 377-384.
|
[18] |
Kumar BR, Tripathi M, Kumari S, et al. The enigma of subnormal vision in persistent pupillary membrane[J]. Med Hypotheses, 2021, 148: 110514.
|
[19] |
Chang M, Ancona-Lezama D, Shields CL. Vascular perfusion in persistent pupillary membrane of the iris[J]. Indian J Ophthalmol, 2019, 67(10): 1704-1705.
|
[20] |
Lambert SR, Buckley EG, Lenhart PD, et al. Congenital fibrovascular pupillary membranes: clinical and histopathologic findings[J]. Ophthalmology, 2012, 119(3): 634-641.
|
[21] |
Khurana S, Gupta PC, Vaiphei K, et al. A clinicopathological study of persistent fetal vasculature[J]. Indian J Ophthalmol, 2019, 67(6): 785-787.
|
[22] |
Prakhunhungsit S, Berrocal AM. Diagnostic and Management Strategies in Patients with Persistent Fetal Vasculature: Current Insights[J]. Clin Ophthalmol, 2020, 14: 4325-4335.
|
[23] |
Paya C, Chan H, Pechméja J, et al. Intraoperative OCT of a Mittendorf dot with persistent hyaloid artery[J]. J Fr Ophtalmol, 2016, 39(1): 109-110.
|
[24] |
Alexandrakis G, Scott IU, Flynn HW, et al. Visual acuity outcomes with and without surgery in patients with persistent fetal vasculature[J]. Ophthalmology, 2000, 107(6): 1068-1072.
|
[25] |
Patel M, Mukherjee D, Farsiu S, et al. Estimation of gestational age via image analysis of anterior lens capsule vascularity in preterm infants: a pilot study[J]. Front Pediatr, 2019, 7: 43.
|
[26] |
Hu A, Pei X, Ding X, et al. Combined persistent fetal vasculature: a classification based on high-resolution B-mode ultrasound and color doppler imaging[J]. Ophthalmology, 2016, 123(1): 19-25.
|
[27] |
赵云娥,胡曼.重视婴幼儿永存胚胎血管的诊断和治疗[J].中华眼视光学与视觉科学杂志,2018,20(1):7-13.
|
[28] |
Laura DM, Staropoli PC, Patel NA, et al. Widefield fluorescein angiography in the fellow eyes of patients with presumed unilateral persistent fetal vasculature[J]. Ophthalmol Retina, 2021, 5(3): 301-307.
|
[29] |
Huang Q, Xu Y, Zhang Q, et al. Peripheral vascular abnormalities detected by fluorescein angiography in contralateral eyes of patients with persistent fetal vasculature[J]. Ophthalmic Surg Lasers Imaging Retina, 2020, 51(9): 506-511.
|
[30] |
Hohberger B, Knorr HLJ, Mardin CY, et al. Bilateral posterior persistent hyperplastic primary vitreous [J]. Ophthalmologe, 2018, 115(8): 680-682.
|
[31] |
Chan LT, Gole GA, Quinn GE, et al. Pathophysiology, screening and treatment of ROP: A multi-disciplinary perspective[J]. Prog Retin Eye Res, 2018, 62: 77-119.
|
[32] |
Tauqeer Z, Yonekawa Y. Familial exudative vitreoretinopathy: pathophysiology, diagnosis, and management[J]. Asia Pac J Ophthalmol (Phila), 2018, 7(3): 176-182.
|
[33] |
Fabian ID, Onadim Z, Karaa E, et al. The management of retinoblastoma[J]. Oncogene, 2018, 37(12): 1551-1560.
|
[34] |
Lagrèze WA. Treatment of congenital and early childhood cataract[J]. Ophthalmologe, 2021, 118(S2): 135-144.
|
[35] |
Aikawa Y, Baba T, Nizawa T, et al. Worsening of retinal detachment after cataract surgery in the eye with persistent fetal vasculature[J]. Case Rep Med, 2021: 6641161.
|
[36] |
Seth NG, Kashyap H, Jurangal A, et al. Ultrasound biomicro-scopic appearance of accessory iris membrane[J]. Indian J Ophthalmol, 2019, 67(1): 122-123.
|
[37] |
Huang YT, Lin HJ. Long term surgical outcome for persistent pupillary membranes with associated ocular abnormalities: a retrospective case series study[J]. BMC Ophthalmol, 2021, 21(1): 232.
|
[38] |
Robb RM. Fibrous congenital iris membranes with pupillary distortion[J]. Trans Am Ophthalmol Soc, 2001, 99: 45-50.
|
[39] |
Gavriᶊ M, Horge I, Avram E, et al. Persistent pupillary membrane or accessary iris membrane? [J]. Rom J Ophthalmol, 2015, 59(3): 184-187.
|
[40] |
Cibis GW, Tripathi RC, Tripathi BJ. Surgical removal of congenital pupillary-iris-lens membrane[J]. Ophthalmic Surg, 1994, 25(9): 580-583.
|
[41] |
梁天蔚,张诚玥,白大勇,等. 先天性纤维血管瞳孔膜的临床特点及治疗分析[J]. 中华眼科杂志,2018,54(11):849-854.
|
[42] |
Wang Q, Zhou F, Chen W, et al. A safe treatment for congenital fibrovascular pupillary membrane[J]. Eur J Ophthalmol, 2020, 30(5): 1143-1148.
|
[43] |
Li L, Fan DB, Zhao YT, et al. Surgical treatment and visual outcomes of cataract with persistent hyperplastic primary vitreous[J]. Int J Ophthalmol, 2017, 10(3): 391-399.
|
[44] |
Sisk RA, Berrocal AM, Feuer WJ, et al. Visual and anatomic outcomes with or without surgery in persistent fetal vasculature[J]. Ophthalmology, 2010, 117(11): 2178-2183.
|
[45] |
Tereshchenko AV, Trifanenkova IG, Vladimirovich VM. Femto-second laser-assisted anterior and posterior capsulotomies in children with persistent hyperplastic primary vitreous[J]. J Cataract Refract Surg, 2020, 46(4): 497-502.
|
[46] |
Bata BM, Chiu HH, Mireskandari K, et al. Long-term visual and anatomic outcomes following early surgery for persistent fetal vasculature: a single-center, 20-year review[J]. J AAPOS, 2019, 23(6): 327.
|
[47] |
Frezzotti R, Bardelli AM, Morocutti A, et al. The pars plana approach in two cases of persistent hyperplastic primary vitreous (PHPV) [J]. Ophthalmic Paediatr Genet, 1984, 4(2): 107-110.
|
[48] |
Khurana S, Ram J, Singh R, et al. Surgical outcomes of cataract surgery in anterior and combined persistent fetal vasculature using a novel surgical technique: a single center, prospective study[J]. Graefes Arch Clin Exp Ophthalmol, 2021, 259(1): 213-221.
|
[49] |
Zahavi A, Weinberger D, Snir M, et al. Management of severe persistent fetal vasculature: case series and review of the literature[J]. Int Ophthalmol, 2019, 39(3): 579-587.
|