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1 ypically similar to the more common disorder Stickler syndrome.
2 metaphyseal dysplasia, Kniest dysplasia, and Stickler syndrome.
3 oma is frequently diagnosed in children with Stickler syndrome.
4 re needed, especially for those with type II Stickler syndrome.
5 us retinal detachment is highly prevalent in Stickler syndrome.
6 tickler syndrome and 30% (n = 6) were type 2 Stickler syndrome.
7 ; I(2) = 82.1%), with higher rates in type 1 Stickler syndrome.
8 ic efficacy, and surgical outcomes of RRD in Stickler syndrome.
9 inical and genetic diagnoses of type I or II Stickler syndrome.
10 t arising from giant retinal tears in type 1 Stickler syndrome.
11 facial, or auditory) usually associated with Stickler syndrome.
12            Among 110 patients with confirmed Stickler syndrome, 90 (82%) had a COL2A1 variant and 20
13 y been found in a family described as having Stickler syndrome, although there was no ocular involvem
14         Seventy percent (n = 14) were type 1 Stickler syndrome and 30% (n = 6) were type 2 Stickler s
15 between 2010-2025 with clinical diagnosis of Stickler syndrome and had at least 2 documented eye exam
16 ed 11 patients with glaucoma, 1 patient with Stickler syndrome, and 1 patient with an IOL exchange at
17             The proportion of types I and II Stickler syndrome are equal in our pediatric population,
18                                          The Stickler syndromes are the most common causes of inherit
19 n XI can give rise to some manifestations of Stickler syndrome, but of these, only mutations in COL11
20 nt and outcomes of glaucoma in children with Stickler syndrome DESIGN: Retrospective observational ca
21 lism of Marshall syndrome with the subset of Stickler syndrome families associated with COL11A1 mutat
22 ents with a confirmed molecular diagnosis of Stickler syndrome followed up in the ophthalmology depar
23                                              Stickler syndrome (hereditary arthro-ophthalmopathy) is
24 22.7% (n = 5) had orofacial manifestation of Stickler syndrome in the form of a cleft palate.
25 irst time that a family with the full Type 2 Stickler syndrome including vitreous and retinal abnorma
26 on distinct from both Wagner disease and the Stickler syndromes indicates that SVD is a distinct gene
27                                              Stickler syndrome is an inherited connective tissue diso
28  that limited visual potential and 1 who had Stickler syndrome), leaving 109 total children analyzed
29 S: Children (less than 18 years of age) with Stickler syndrome METHODS: Review of 97 patients who pre
30 nking COL2A1 and COL11A1, the known loci for Stickler syndrome; mutation screening of COL2A1; constru
31 1-related/type I and COL11A1-related/type II Stickler syndrome (n = 13; 50%) and included 12 previous
32 ta suggest that PHOMS are a novel finding in Stickler syndrome patients and should be considered when
33       In the largest global cohort of type 1 Stickler syndrome patients published, all analyses indic
34  phenotypic optic disc abnormalities from 11 Stickler syndrome patients were identified and imaged.
35 y-two eyes with anomalous optic disc from 11 Stickler syndrome patients were identified and imaged.
36 y (SD-OCT) features of high myopic eyes with Stickler syndrome (STL) with matched controls.
37 r intragenic to the genes for the 18p locus, Stickler syndromes type I and II (12q13.1-q13.3 and 6p21
38                                Families with Sticklers syndrome type 1 have a characteristic congenit
39 kers flanking or intragenic to the genes for Stickler syndrome types 1 and 2 (chromosomes 12q13.1-q13
40 nce of linkage was found for markers for the Stickler syndrome types 1 and 2, the Marfan syndrome, or
41  by using intragenic or flanking markers for Stickler syndrome types 1, 2, and 2B; Marfan syndrome; E
42 atogenous retinal detachment associated with Stickler syndrome was more likely to occur in the younge
43  RESULTS: Fourteen of 97 patients (14%) with Stickler Syndrome were diagnosed with glaucoma at median
44  data in genetically or clinically confirmed Stickler syndrome were included.
45 fference between COL2A1- and COL11A1-related Stickler syndrome, with COL11A1 variants potentially ass