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Quoted phrase not found in phrase index: "Hypoplasia of the iris dilator muscle"
Page 1
Pupillary Abnormalities in Descemet Membrane Endothelial Keratoplasty After Nearly Full Tamponade.
Arnalich-Montiel F, Pérez-Sarriegui A, Lauzirika G, Porrua L, Hernández-Verdejo JL. Arnalich-Montiel F, et al. Cornea. 2017 Mar;36(3):290-294. doi: 10.1097/ICO.0000000000001141. Cornea. 2017. PMID: 28129299
These abnormalities were not related to morphometric changes in the iris volume, or in the iris dilator or iris sphincter muscle, but were probably due to posterior synechiae. Combining DMEK and cataract surgery increases by 5-fold the od …
These abnormalities were not related to morphometric changes in the iris volume, or in the iris dilator or ir …
Study on the correlation between iris blood flow, iris thickness and pupil diameter in the resting state and after pharmacological mydriasis in patients with diabetes mellitus.
Cui L, Xiao Y, Xiang Z, Chen Z, Yang C, Zou H. Cui L, et al. BMC Ophthalmol. 2024 Feb 2;24(1):52. doi: 10.1186/s12886-024-03322-y. BMC Ophthalmol. 2024. PMID: 38308203 Free PMC article. Clinical Trial.
BACKGROUND: To investigate whether iris blood flow and iris thickness at the iris smooth muscle region affect the pupil diameter at rest and after drug-induced mydriasis in patients with type 1 diabetes mellitus (T1DM) and type 2 diabetes mellitus (T2D …
BACKGROUND: To investigate whether iris blood flow and iris thickness at the iris smooth muscle region affect th …
Congenital aplasia of the iris sphincter and dilator muscles.
Buys Y, Buncic JR, Enzenauer RW, Mednick E, O'Keefe M. Buys Y, et al. Can J Ophthalmol. 1993 Apr;28(2):72-5. Can J Ophthalmol. 1993. PMID: 8508341
Congenital aplasia of the iris sphincter and dilator muscles is rare. We describe a 3-month-old boy with a patent ductus arteriosus who had this anomaly, with no other ocular or systemic abnormalities. ...This anomaly, although it bears some similarity …
Congenital aplasia of the iris sphincter and dilator muscles is rare. We describe a 3-month-old boy with a patent ductu …
First evidence of maternally inherited mosaicism in TGFBR1 and subtle primary myocardial changes in Loeys-Dietz syndrome: a case report.
Baban A, Magliozzi M, Loeys B, Adorisio R, Alesi V, Secinaro A, Corica B, Vricella L, Dietz HC, Drago F, Novelli A, Amodeo A. Baban A, et al. BMC Med Genet. 2018 Sep 15;19(1):170. doi: 10.1186/s12881-018-0661-2. BMC Med Genet. 2018. PMID: 30219046 Free PMC article.
BACKGROUND: Loeys-Dietz syndrome (LDS) is a rare multisystemic disorder characterized by vascular and skeletal abnormalities, with considerable intra- and interfamilial variability. CASE PRESENTATION: We report the case of an 8-year-old male with clinical features of two d …
BACKGROUND: Loeys-Dietz syndrome (LDS) is a rare multisystemic disorder characterized by vascular and skeletal abnormalities, with co …