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1 in two unrelated Lowe syndrome patients with congenital glaucoma.
2 s the initial surgical procedure for primary congenital glaucoma.
3 cup-to-disc (C/D) ratio greater in secondary congenital glaucoma.
4 ve changes, occlusion of the visual axis, or congenital glaucoma.
5                    Most patients had primary congenital glaucoma (80%).
6                                   In primary congenital glaucoma, a positive correlation was noted be
7             Most cases (80%) were of primary congenital glaucoma after failed goniotomy surgery.
8 ts (60 eyes) analyzed with bilateral primary congenital glaucoma aged </=2 years, 1 eye of each patie
9 atients with unilateral or bilateral primary congenital glaucoma aged less than 2 years were randomiz
10 f the 6p25 breakpoint in a patient with both congenital glaucoma and a balanced-translocation event i
11 l length was significantly longer in primary congenital glaucoma and cup-to-disc (C/D) ratio greater
12 Although most glaucoma patients are elderly, congenital glaucoma and glaucomas of childhood are also
13 iscusses the roles of these genes in primary congenital glaucoma and glaucomas of childhood.
14  in humans with genetic eye diseases such as congenital glaucoma and microspherophakia, indicating a
15 hy with a predilection for the macular area, congenital glaucoma and optical nerve hypoplasia, and op
16 try provides unique baseline data on primary congenital glaucoma and secondary congenital glaucoma in
17                                 Most primary congenital glaucoma and secondary congenital glaucoma pa
18 venile GLC1A glaucoma, a P450 gene for GLC3A congenital glaucoma, and a bicoidhomeobox transcription
19 p25 region is now implicated in FGI, primary congenital glaucoma, and iridogoniodysgenesis anomaly.
20 tter for specific diagnoses, such as primary congenital glaucoma, aphakic glaucoma, and glaucomas ass
21  syndrome, a rare condition characterized by congenital glaucoma, as well as craniofacial, skeletal,
22 d clinical features of primary and secondary congenital glaucoma at presentation.
23                                      Primary congenital glaucoma (Buphthalmos) is an autosomal recess
24                                              Congenital glaucoma (CG) is a heterogeneous, inherited a
25      Five patients (12%) were diagnosed with congenital glaucoma, characterized by the clinical triad
26                       First-line surgery for congenital glaucoma consists of incisional procedures on
27                                Seven primary congenital glaucoma families (14.9%) manifested disease
28                                  One primary congenital glaucoma family possessed homozygous mutant a
29             Sanger sequencing of the primary congenital glaucoma gene, CYP1B1, was performed on 47 pr
30                                      Primary congenital glaucoma (gene symbol: GLC3) is an ocular dis
31 ients who have no mutations in known primary congenital glaucoma genes.
32                               In the primary congenital glaucoma group, corneal haze showed a signifi
33 on primary congenital glaucoma and secondary congenital glaucoma in Saudi Arabia that will enable us
34                                              Congenital glaucoma is primarily a surgical disease with
35  and GLC3B) have been identified for primary congenital glaucoma, one locus (GLC1A) for juvenile-onse
36 atio and corneal haze, whereas for secondary congenital glaucoma only axial length was positively cor
37 The medical records of patients with primary congenital glaucoma over a 23-year period were reviewed:
38                          Fifty-seven primary congenital glaucoma patients (47 families), 71 unaffecte
39 2, and MYOC mutations in a cohort of primary congenital glaucoma patients from the United States, app
40 st primary congenital glaucoma and secondary congenital glaucoma patients had bilateral disease (82.6
41 uencing, may identify novel genes in primary congenital glaucoma patients who have no mutations in kn
42 The annual incidence of diagnosis of primary congenital glaucoma (PCG) in Great Britain was 5.41 in 1
43                                      Primary congenital glaucoma (PCG) is a devastating eye disease a
44                                      Primary congenital glaucoma (PCG) is a leading cause of blindnes
45                                      Primary congenital glaucoma (PCG) is an autosomal recessive diso
46                                      Primary congenital glaucoma (PCG) is an autosomal recessive ocul
47                                      Primary congenital glaucoma (PCG) is an autosomal-recessive cond
48     The autosomal recessive disorder primary congenital glaucoma (PCG) is caused by unknown developme
49                                      Primary congenital glaucoma (PCG) is isolated, non-syndromic gla
50  gene (CYP1B1) in five families with primary congenital glaucoma (PCG) linked to the GLC3A locus on c
51               We have identified two primary congenital glaucoma (PCG) patients with chromosomal anom
52 uvenile open-angle glaucoma (OAG) or primary congenital glaucoma (PCG) with sustained postoperative i
53 ubject groups: two Siamese cats with primary congenital glaucoma (PCG), a control Siamese cat without
54 t of conventional angle surgeries in primary congenital glaucoma (PCG), as judged by glaucoma and vis
55 onal partial trabeculotomy (CPT) for primary congenital glaucoma (PCG).
56 B1) gene are a common cause of human primary congenital glaucoma (PCG).
57               Concurrently, 33 of 47 primary congenital glaucoma probands with extended family deoxyr
58  71 unaffected family members of the primary congenital glaucoma probands, and 101 healthy unrelated
59                                          The congenital glaucoma registry provides unique baseline da
60 angle surgeries show good success in primary congenital glaucoma, reported success in glaucoma follow
61 rrelation of OCRL1 mutations associated with congenital glaucoma revealed clustering of missense and
62 egistry data that included new patients with congenital glaucoma seen between 2001 and 2003 (29 month
63  coincide with a mutation of Tie2 in primary congenital glaucoma that leads to defective Tie2 cluster
64 f a new locus (designated GLC3B) for primary congenital glaucoma to the short arm of chromosome 1 (1p
65 was equally distributed by sex but secondary congenital glaucoma was 1.5-fold more common in male pat
66 ean (+/- SD) age at presentation for primary congenital glaucoma was 3.8 +/- 10.7 months and for seco
67 ma was 3.8 +/- 10.7 months and for secondary congenital glaucoma was 4.3 +/- 7.9 months.
68                                      Primary congenital glaucoma was equally distributed by sex but s
69                                      Primary congenital glaucoma was present in 39 eyes (88.6%), apha
70        Some causes of visual loss (including congenital glaucoma with buphthalmos and retinal detachm

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