ライフサイエンスコーパス: congenital glaucoma

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 was 18.07 +/- 13.97 months; 78% had primary congenital glaucoma.

6 mferential GATT for IOP control in eyes with congenital glaucoma.

7 The main indication was congenital glaucoma (29.4%).

8 Most patients had primary congenital glaucoma (80%).

9 In primary congenital glaucoma, a positive correlation was noted be

10 and ethnically diverse families affected by congenital glaucoma, a severe form of glaucoma affecting

11 Most cases (80%) were of primary congenital glaucoma after failed goniotomy surgery.

12 ts (60 eyes) analyzed with bilateral primary congenital glaucoma aged </=2 years, 1 eye of each patie

13 atients with unilateral or bilateral primary congenital glaucoma aged less than 2 years were randomiz

14 f the 6p25 breakpoint in a patient with both congenital glaucoma and a balanced-translocation event i

15 l length was significantly longer in primary congenital glaucoma and cup-to-disc (C/D) ratio greater

16 Although most glaucoma patients are elderly, congenital glaucoma and glaucomas of childhood are also

17 iscusses the roles of these genes in primary congenital glaucoma and glaucomas of childhood.

18 in humans with genetic eye diseases such as congenital glaucoma and microspherophakia, indicating a

19 hy with a predilection for the macular area, congenital glaucoma and optical nerve hypoplasia, and op

20 try provides unique baseline data on primary congenital glaucoma and secondary congenital glaucoma in

21 Most primary congenital glaucoma and secondary congenital glaucoma pa

22 venile GLC1A glaucoma, a P450 gene for GLC3A congenital glaucoma, and a bicoidhomeobox transcription

23 p25 region is now implicated in FGI, primary congenital glaucoma, and iridogoniodysgenesis anomaly.

24 two daughters were undergoing treatment for congenital glaucoma, and one of the daughters also had f

25 tter for specific diagnoses, such as primary congenital glaucoma, aphakic glaucoma, and glaucomas ass

26 syndrome, a rare condition characterized by congenital glaucoma, as well as craniofacial, skeletal,

27 d clinical features of primary and secondary congenital glaucoma at presentation.

28 Primary congenital glaucoma (Buphthalmos) is an autosomal recess

29 Congenital glaucoma (CG) is a heterogeneous, inherited a

30 Five patients (12%) were diagnosed with congenital glaucoma, characterized by the clinical triad

31 First-line surgery for congenital glaucoma consists of incisional procedures on

32 Seven primary congenital glaucoma families (14.9%) manifested disease

33 One primary congenital glaucoma family possessed homozygous mutant a

34 Sanger sequencing of the primary congenital glaucoma gene, CYP1B1, was performed on 47 pr

35 Primary congenital glaucoma (gene symbol: GLC3) is an ocular dis

36 ients who have no mutations in known primary congenital glaucoma genes.

37 In the primary congenital glaucoma group, corneal haze showed a signifi

38 anomalies (HR, 12; P = 0.0054), and primary congenital glaucoma (HR, 5.4; P = 0.041).

39 inase TEK or its ligand ANGPT1 cause primary congenital glaucoma in humans and mice due to failure of

40 on primary congenital glaucoma and secondary congenital glaucoma in Saudi Arabia that will enable us

41 Congenital glaucoma is primarily a surgical disease with

42 pared with those with neonatal-onset primary congenital glaucoma (N-PCG).

43 mmon, while in India and Iran it was primary congenital glaucoma neonatal onset.

44 and GLC3B) have been identified for primary congenital glaucoma, one locus (GLC1A) for juvenile-onse

45 atio and corneal haze, whereas for secondary congenital glaucoma only axial length was positively cor

46 The medical records of patients with primary congenital glaucoma over a 23-year period were reviewed:

47 Fifty-seven primary congenital glaucoma patients (47 families), 71 unaffecte

48 Primary congenital glaucoma patients from Northern Portugal with

49 2, and MYOC mutations in a cohort of primary congenital glaucoma patients from the United States, app

50 st primary congenital glaucoma and secondary congenital glaucoma patients had bilateral disease (82.6

51 uencing, may identify novel genes in primary congenital glaucoma patients who have no mutations in kn

52 Diagnoses included primary congenital glaucoma (PCG n = 22), juvenile open angle gl

53 s (80 eyes) were identified, 42 with primary congenital glaucoma (PCG) and 3 with juvenile open angle

54 gle surgery were 34.5% and 39.2% for primary congenital glaucoma (PCG) and juvenile open-angle glauco

55 Primary congenital glaucoma (PCG) comprised the single largest g

56 ommon type of childhood glaucoma was primary congenital glaucoma (PCG) constituting (42%, n = 76 eyes

57 ieved in 81% (95% CI 57.4%-93.7%) of primary congenital glaucoma (PCG) eyes.

58 The annual incidence of diagnosis of primary congenital glaucoma (PCG) in Great Britain was 5.41 in 1

59 Primary congenital glaucoma (PCG) is a devastating eye disease a

60 Primary congenital glaucoma (PCG) is a leading cause of blindnes

61 Primary congenital glaucoma (PCG) is a potentially blinding dise

62 Primary congenital glaucoma (PCG) is a severe disease characteri

63 Primary congenital glaucoma (PCG) is an autosomal recessive diso

64 Primary congenital glaucoma (PCG) is an autosomal recessive ocul

65 Primary congenital glaucoma (PCG) is an autosomal-recessive cond

66 The autosomal recessive disorder primary congenital glaucoma (PCG) is caused by unknown developme

67 Primary congenital glaucoma (PCG) is isolated, non-syndromic gla

68 gene (CYP1B1) in five families with primary congenital glaucoma (PCG) linked to the GLC3A locus on c

69 nd life satisfaction (LS) of treated primary congenital glaucoma (PCG) patients in adulthood.

70 We have identified two primary congenital glaucoma (PCG) patients with chromosomal anom

71 Primary congenital glaucoma (PCG) was the most common diagnosis

72 uvenile open-angle glaucoma (OAG) or primary congenital glaucoma (PCG) with sustained postoperative i

73 n billing codes, 208 eyes (4.1%) had primary congenital glaucoma (PCG), 1911 eyes (38.1%) had juvenil

74 ubject groups: two Siamese cats with primary congenital glaucoma (PCG), a control Siamese cat without

75 individuals (167/290, 303 eyes) had primary congenital glaucoma (PCG), and 19.3% (56/290, 109 eyes)

76 t of conventional angle surgeries in primary congenital glaucoma (PCG), as judged by glaucoma and vis

77 To delineate the genetic bases of primary congenital glaucoma (PCG), we ascertained a large cohort

78 onal partial trabeculotomy (CPT) for primary congenital glaucoma (PCG).

79 B1) gene are a common cause of human primary congenital glaucoma (PCG).

80 alth on presentation and outcomes in primary congenital glaucoma (PCG).

81 ) is proposed in the pathogenesis of primary congenital glaucoma (PCG).

82 eculotomy (GATT) in the treatment of primary congenital glaucoma (PCG).

83 w-up, 1-2 months later, in eyes with primary congenital glaucoma (PCG; n=6).

84 Concurrently, 33 of 47 primary congenital glaucoma probands with extended family deoxyr

85 71 unaffected family members of the primary congenital glaucoma probands, and 101 healthy unrelated

86 Questionnaire) and the CarCGQoL (Caregivers Congenital Glaucoma QOL Questionnaire).

87 The congenital glaucoma registry provides unique baseline da

88 angle surgeries show good success in primary congenital glaucoma, reported success in glaucoma follow

89 rrelation of OCRL1 mutations associated with congenital glaucoma revealed clustering of missense and

90 egistry data that included new patients with congenital glaucoma seen between 2001 and 2003 (29 month

91 coincide with a mutation of Tie2 in primary congenital glaucoma that leads to defective Tie2 cluster

92 f a new locus (designated GLC3B) for primary congenital glaucoma to the short arm of chromosome 1 (1p

93 was equally distributed by sex but secondary congenital glaucoma was 1.5-fold more common in male pat

94 ean (+/- SD) age at presentation for primary congenital glaucoma was 3.8 +/- 10.7 months and for seco

95 ma was 3.8 +/- 10.7 months and for secondary congenital glaucoma was 4.3 +/- 7.9 months.

96 Primary congenital glaucoma was equally distributed by sex but s

97 Primary congenital glaucoma was present in 39 eyes (88.6%), apha

98 Congenital glaucoma was the main indication for corneal

99 Primary congenital glaucoma was the most common diagnosis (12 ey

100 Rejection and diagnosis of congenital glaucoma were risk factors for graft failure.

101 panel diagnostic of 18 genes associated with congenital glaucoma, whole exome sequencing was performe

102 Some causes of visual loss (including congenital glaucoma with buphthalmos and retinal detachm