Axenfeld-Rieger Syndrome and Peters' Anomaly

Cornea ◽  
2011 ◽  
pp. 655-664
Author(s):  
Mansi Parikh ◽  
Wallace L.M. Alward
Medicine ◽  
2022 ◽  
Vol 101 (2) ◽  
pp. e21213
Author(s):  
Yong Meng ◽  
Guohua Lu ◽  
Yang Xie ◽  
Xincheng Sun ◽  
Liqin Huang

2003 ◽  
Vol 135 (3) ◽  
pp. 368-375 ◽  
Author(s):  
Robert A Honkanen ◽  
Darryl Y Nishimura ◽  
Ruth E Swiderski ◽  
Steven R Bennett ◽  
Sungpyo Hong ◽  
...  

2008 ◽  
Vol 74 (5) ◽  
pp. 476-480 ◽  
Author(s):  
N Weisschuh ◽  
C Wolf ◽  
B Wissinger ◽  
E Gramer

1991 ◽  
Vol 28 (4) ◽  
pp. 277-279 ◽  
Author(s):  
J C de Almeida ◽  
D F Reis ◽  
J Llerena Junior ◽  
J Barbosa Neto ◽  
R L Pontes ◽  
...  

1996 ◽  
Vol 210 (6) ◽  
pp. 361-366 ◽  
Author(s):  
Charlise A. Gunderson ◽  
Robert Stone ◽  
Robert Peiffer ◽  
Sharon Freedman

2021 ◽  
Vol 6 (1) ◽  
Author(s):  
Mingsen Li ◽  
Liqiong Zhu ◽  
Jiafeng Liu ◽  
Huaxing Huang ◽  
Huizhen Guo ◽  
...  

AbstractForkhead box C1 (FOXC1) is required for neural crest and ocular development, and mutations in FOXC1 lead to inherited Axenfeld–Rieger syndrome. Here, we find that FOXC1 and paired box 6 (PAX6) are co-expressed in the human limbus and central corneal epithelium. Deficiency of FOXC1 and alternation in epithelial features occur in patients with corneal ulcers. FOXC1 governs the fate of the corneal epithelium by directly binding to lineage-specific open promoters or enhancers marked by H3K4me2. FOXC1 depletion not only activates the keratinization pathway and reprograms corneal epithelial cells into skin-like epithelial cells, but also disrupts the collagen metabolic process and interferon signaling pathways. Loss of interferon regulatory factor 1 and PAX6 induced by FOXC1 dysfunction is linked to the corneal ulcer. Collectively, our results reveal a FOXC1-mediated regulatory network responsible for corneal epithelial homeostasis and provide a potential therapeutic target for corneal ulcer.


PEDIATRICS ◽  
1992 ◽  
Vol 90 (1) ◽  
pp. 47-49
Author(s):  
Aengus S. O'Marcaigh ◽  
Lora B. Folz ◽  
Virginia V. Michels

Malformations of the umbilicus are a feature of many dysmorphic syndromes including Rieger syndrome, Robinow syndrome, and Aarskog syndrome. The characteristic umbilical malformation in Rieger syndrome consists of redundant periumbilical skin which extends along the cord for an excessive distance. Although the measurement of umbilical skin length plays an important role in the neonatal diagnosis of Rieger syndrome, normal values for this measurement in healthy neonates have not been established. Umbilical skin length was measured in 104 healthy neonates. The length to which the umbilical skin extended along the cranial aspect of cord (mean 11.53 mm, SD 3.58) was significantly longer than the umbilical skin length along the caudal aspect (mean 8.71 mm, SD 2.89) (P < .05). Multiple regression analysis revealed a significant association between age and umbilical skin length. Birth weight, length, and gestational age were not significantly associated with umbilical skin length when adjusted for the other three variables. No significant differences in umbilical skin length were observed between male and female groups. The above normal values should aid in the neonatal diagnosis of Rieger syndrome, and furthermore it is recommended that cranial umbilical skin length measurement be included in the examination of the dysmorphic child.


1987 ◽  
Vol 24 (4) ◽  
pp. 198-203
Author(s):  
Rena A Stathacopoulos ◽  
J Bronwyn Bateman ◽  
Robert S Sparkes ◽  
Robert S Hepler

2019 ◽  
Vol 2 (4) ◽  
pp. 266
Author(s):  
Ze Zhang ◽  
Nasreen A. Syed ◽  
Wallace L.M. Alward
Keyword(s):  

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