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1 iridia, foveal hypoplasia, and laterality of congenital cataract.
2 d in children who are born with a unilateral congenital cataract.
3 nes previously described in association with congenital cataract.
4 g has been a mainstay in treating unilateral congenital cataract.
5 ual acuity in infants treated for unilateral congenital cataract.
6 tion (n = 57) in 114 infants with unilateral congenital cataract.
7  contact lens in 114 infants with unilateral congenital cataract.
8 ontact lens in 114 infants with a unilateral congenital cataract.
9 d clinical trial of treatment for unilateral congenital cataract.
10 ren less than 7 months old with a unilateral congenital cataract.
11 ding lens alpha-crystallin mutants linked to congenital cataract.
12  of stability, is the primary basis for P23T congenital cataracts.
13 ity tag, and lens tissue from a patient with congenital cataracts.
14 hypoplasia, autosomal dominant keratitis and congenital cataracts.
15  the pathogenesis of alphaA R116C associated congenital cataracts.
16 ally defective AQP0 protein from humans with congenital cataracts.
17 re than 12 different genetic loci that cause congenital cataracts.
18  lenses using endogenous stem cells to treat congenital cataracts.
19 lly linked to one form of autosomal dominant congenital cataracts.
20 '-end of the gene occurred in a patient with congenital cataracts.
21 ye was advocated for infants with unilateral congenital cataracts.
22 man gammaD-crystallin mutant associated with congenital cataracts.
23 onatal diabetes, sensorineural deafness, and congenital cataracts.
24 -generation pedigree with autosomal dominant congenital cataracts.
25 cell differentiation, defects in which cause congenital cataracts.
26 ugh to get good visual and motor outcomes in congenital cataracts.
27 hasizes the importance of genetic testing of congenital cataracts.
28 ctrum and frequency of genes responsible for congenital cataracts.
29 associated genes in 27 Chinese families with congenital cataracts.
30 utation spectrum of Cx50 in association with congenital cataracts.
31 1R and G588S) in two families with extensive congenital cataracts.
32 ft after amino acid 255 and causes recessive congenital cataracts.
33 s include nephrogenic diabetes insipidus and congenital cataracts.
34 f the brain, subependymal calcification, and congenital cataracts.
35 ystallin, the P23T mutant is associated with congenital cataracts.
36 nal mutant connexin46 (CX46) associated with congenital cataracts.
37  Pakistani families with autosomal recessive congenital cataracts.
38 in gene have been linked to several types of congenital cataracts.
39 an, lamellar, coralliform, and fasciculiform congenital cataracts.
40            Thirty-nine (53.4%) suffered from congenital cataract, 10 unilateral (25.7%) and 29 bilate
41            Seventy-four (45.1%) children had congenital cataract, 31.1% had developmental cataract, a
42 l deafness diagnosed soon after birth (5/5), congenital cataracts (4/5), and hypotonia (4/5).
43 f all cases are familial; autosomal dominant congenital cataract (ADCC) appears to be the most common
44                           Autosomal dominant congenital cataracts (ADCC) are clinically and genetical
45 ighly penetrant, autosomal dominant forms of congenital cataracts (ADCC) are most common.
46 als who had been treated for dense bilateral congenital cataracts, after an average of 12 years of bl
47 dicate that crystallin mutations involved in congenital cataracts altered protein-protein interaction
48 reated with 1 of 2 treatments for unilateral congenital cataract and followed up to 5 years of age.
49                                        Human congenital cataract and ocular anterior segment dysgenes
50 carring as a result of vitamin A deficiency, congenital cataract and retinopathy of prematurity.
51                 Early surgery for unilateral congenital cataract and the presence of visual acuity be
52                   Xcat mice display X-linked congenital cataracts and are a mouse model for the human
53 linked congenital disease that presents with congenital cataracts and glaucoma, as well as renal and
54 -linked congenital disorder characterized by congenital cataracts and glaucoma, mental retardation an
55 i-organ disease bronchio-oto-renal syndrome, congenital cataracts and late-onset deafness.
56 almia-anophthalmia-coloboma (MAC; 86 genes), congenital cataracts and lens-associated conditions (70
57 ed); RET, 42.8% (21 of 49 cases solved); and congenital cataracts and lens-associated conditions, 88.
58 The vacuolated lens (vl) mouse mutant causes congenital cataracts and neural tube defects (NTDs), wit
59 branchio-oto-renal (BOR) syndrome as well as congenital cataracts and ocular defects (OD).
60 terized by cognitive deficiencies, bilateral congenital cataracts and renal dysfunction.
61  a distant history of prior intervention for congenital cataracts and was presumed to be aphakic.
62 ted with the common disorders of strabismus, congenital cataract, and amblyopia.
63  disease characterized by renal tubulopathy, congenital cataracts, and mental retardation, is associa
64 isorder characterized by mental retardation, congenital cataracts, and renal tubular dysfunction.
65 e including neonatal/infancy-onset diabetes, congenital cataracts, and sensorineural deafness.
66 sults in forms of Peters anomaly, unilateral congenital cataracts, and the morning glory disc anomaly
67 inimum UAT was significantly associated with congenital cataracts (aOR = 1.51; 95% CI: 1.14, 1.99).
68 f all cases are familial; autosomal-dominant congenital cataract appears to be the most-common famili
69                          Autosomal-recessive congenital cataracts (arCC) form a clinically diverse an
70                                              Congenital cataracts are a common major abnormality of t
71 s can be very challenging in some cases, for congenital cataracts are clinically and genetically hete
72      Recovery studies after removal of dense congenital cataracts are examples of this, but most are
73                                              Congenital cataracts are one of the most common major ey
74                        An autosomal dominant congenital cataract associated with a missense mutation,
75 r impetus for the treatment of children with congenital cataract at the earliest possible age.
76 up that involved 114 infants with unilateral congenital cataracts at 12 sites.
77  cell denucleation (LFCD) is associated with congenital cataracts, but the pathobiology awaits elucid
78 enile-onset cataracts are distinguished from congenital cataracts by the initial clarity of the lens
79                                              Congenital cataracts (CCs), responsible for about one-th
80 he locus for the clinically distinct Volkman congenital cataract (CCV).
81 isolated (Dent disease 2) or associated with congenital cataracts, central hypotonia and intellectual
82 ome is an X-linked disorder characterized by congenital cataracts, cognitive disability, and proximal
83 reatment cost of an infant with a unilateral congenital cataract corrected optically with an IOL was
84  following crystallin genes involved in some congenital cataracts: CRYAA (R116C), CRYAB (R120G), and
85                                              Congenital cataract crystallin genes were cloned and fus
86                We previously mapped X-linked congenital cataract (CXN) in one family to an interval o
87 imated yearly incidence of the syndrome from congenital cataract data for births between 1990 and 200
88 a variety of ocular abnormalities, including congenital cataracts, decreased retinal function, and ha
89 P49/BFSP2 gene have been linked to familial, congenital cataract, demonstrating an important role of
90 nked developmental disorder characterized by congenital cataract, dental anomalies, facial dysmorphis
91 HS) is an X-linked disorder characterized by congenital cataracts, dental anomalies, dysmorphic featu
92 pmental disorder, characterized by bilateral congenital cataracts, dental anomalies, facial dysmorphi
93 documentation of aphakia after treatment for congenital cataracts, detailed workup revealed residual
94                     Eight of 9 patients with congenital cataracts developed glaucoma, and 8 of 8 pati
95 g in Ethiopian patients with early bilateral congenital cataracts diagnosed and treated by us only at
96      This report suggests that patients with congenital cataract due to some GJA3 genetic variants ma
97 tive complications among family members with congenital cataract due to the p.Asp67Tyr GJA3 genetic v
98          In humans, GK deficiency results in congenital cataracts due to an accumulation of galactito
99 hin mapped genomic intervals associated with congenital cataract for further investigation.
100 a, hyperferritinemia with autosomal dominant congenital cataract, Friedreich's ataxia, and X-linked s
101 ges in protein-protein interactions of those congenital cataract gene products with the three major c
102 ability, early-onset epilepsy, microcephaly, congenital cataracts, growth retardation, and spasticity
103                Key clinical features include congenital cataracts, hypotonia, prenatal-onset ventricu
104 the limbs, contractures, facial dysmorphism, congenital cataracts, ichthyosis, spasticity, microcepha
105 forms is associated with autosomal recessive congenital cataract in four distantly related Arab famil
106                        An autosomal dominant congenital cataract in human is associated with mutation
107                        An autosomal dominant congenital cataract in humans is associated with mutatio
108 tant of gammaD-crystallin is associated with congenital cataract in mice and was previously shown to
109 linical trial of 114 infants with unilateral congenital cataract in referral centers who were between
110  variant in the GJA3 gene is responsible for congenital cataracts in a family with a high incidence o
111 n alphaA-crystallin has been associated with congenital cataracts in humans.
112 or segment mesenchymal dysgenesis (ASMD) and congenital cataracts in humans.
113 f the underlying genetic causes of bilateral congenital cataract, including novel disease-causing var
114 se may have different pathogenic mechanisms: Congenital cataracts induce the unfolded protein respons
115                           Autosomal dominant congenital cataract is a clinically and genetically hete
116                                              Congenital cataract is a leading cause of visual disabil
117                                              Congenital cataract is both clinically diverse and genet
118  The mechanism of amblyopia in children with congenital cataract is not understood fully, but studies
119                                              Congenital cataract is the most frequent inherited ocula
120 ment of amblyopia associated with unilateral congenital cataracts is evolving.
121 ypothesis predicts that children treated for congenital cataracts late in life will exhibit persisten
122 L cause Lowe syndrome (LS), characterized by congenital cataract, low IQ, and defective kidney proxim
123                                 This form of congenital cataracts maps to a 12-cM region on chromosom
124 ) is a multisystem disorder characterized by congenital cataracts, mental retardation, and renal Fanc
125 t with psoriasiform dermatitis, arthralgias, congenital cataracts, microcephaly, and developmental de
126  developmental ocular disorders that include congenital cataract, microcornea, coloboma and anterior
127 ersistent fetal vasculature, microphthalmia, congenital cataracts, microcornea, corneal opacity and n
128 n two consanguineous Pakistani families with congenital cataract-microcornea with mild to moderate co
129         Spiroplasma as a very rare cause for congenital cataract might be underdiagnosed.
130 stallin mutants, W42R and W42Q: the former a congenital cataract mutation, and the latter a mimic of
131 eted next-generation sequencing in inherited congenital cataract patients provided significant diagno
132 well-described motion perception deficits in congenital cataract patients.
133 p.Asp67Tyr, was identified in a 4-generation congenital cataract pedigree from Iowa.
134 tic disease characterized by the presence of congenital cataracts, profound learning disabilities and
135 unctata, coronal clefts, cervical dysplasia, congenital cataracts, profound postnatal growth retardat
136 male lethality and comprises microphthalmia, congenital cataracts, radiculomegaly, and cardiac and di
137 e observations of an adult case of bilateral congenital cataract removal, we have found evidence that
138 vs aphakia, and optimal timing of unilateral congenital cataract removal.
139 X-linked disorder characterized by bilateral congenital cataracts, renal Fanconi syndrome, and mental
140 , mice deficient in Ocrl1 do not develop the congenital cataracts, renal Fanconi syndrome, or neurolo
141 ocular eyelid suture, a laboratory model for congenital cataract, results in shrinkage of ocular domi
142                                       In the congenital cataract-reversal group, a lower Glx/GABA+ ra
143                           Across conditions, congenital cataract-reversal individuals demonstrated a
144                       The lower E/I ratio in congenital cataract-reversal individuals would thus be a
145                            The laterality of congenital cataracts seems to affect the type of strabis
146  in young individuals surgically treated for congenital cataracts several years after birth.
147                    Individuals with reversed congenital cataracts showed a bias towards perceiving vi
148 se reported by 1721 that he had performed 36 congenital cataract surgeries, with the youngest patient
149 rs, and the most common cause of aphakia was congenital cataract surgery (55%).
150 ict future glaucoma among infants undergoing congenital cataract surgery and provide a risk calculato
151 A retrospective analysis of patients who had congenital cataract surgery and secondary intraocular le
152 secondary IOL implantation for aphakia after congenital cataract surgery at L. V. Prasad Eye Institut
153 n analysis of 112 infants who had unilateral congenital cataract surgery between 1-6 months of chrono
154  the author of the next identified report of congenital cataract surgery in 1706, stated that he was
155           Long-term monitoring of eyes after congenital cataract surgery is important because we esti
156                           Glaucoma following congenital cataract surgery is the most common secondary
157               Beginning in the 17th century, congenital cataract surgery permitted surgeons to tout t
158 rm visual and ocular motility outcomes after congenital cataract surgery remain limited.
159                    The earliest reference to congenital cataract surgery that we identified, reported
160 ords of 62 eyes of 37 children who underwent congenital cataract surgery when <7 months of age by the
161 hthalmology Clinic in Bialystok for left eye congenital cataract surgery.
162 nificant association with glaucoma following congenital cataract surgery.
163 ous sight-threatening complication following congenital cataract surgery.
164 ma suspect diagnosis at 10.5 years following congenital cataract surgery.
165 9.5% (95% CI: 10.0%-36.1%) by 10 years after congenital cataract surgery.
166 nt the early development of strabismus after congenital cataract surgery.
167           The median age at presentation for congenital cataracts that were noticed by the mother was
168 tand the role of Cx50 in the pathogenesis of congenital cataract, the functional consequences of the
169 ls containing genes associated with isolated congenital cataract, the mutant gene is ranked within th
170 ith a history of developmental or incomplete congenital cataracts, the well-known enhancement of the
171 y with the clinical phenotypes--ranging from congenital cataracts to nephrogenic diabetes insipidus.
172 chieving near normal vision after unilateral congenital cataract (UCC) surgery is possible but requir
173 Median age at presentation for patients with congenital cataract was 18 months and 84 months for deve
174 laucoma suspect) after removal of unilateral congenital cataract was not associated with worse visual
175  individuals affected by autosomal recessive congenital cataracts was ascertained.
176 ening of a panel of patients with hereditary congenital cataract we identified a mutation in MAF in a
177  of a Chinese family with autosomal dominant congenital cataracts, we recruited family members who un
178 5 families with different types of bilateral congenital cataract were included.
179 sed with nonsyndromic or syndromic bilateral congenital cataract were selected for investigation thro
180      Within the childhood cataract category, congenital cataracts were more prominent (7.1%).
181                                              Congenital cataracts were significantly associated with
182 during the relevant developmental window and congenital cataracts which should be confirmed with othe
183 ions causing severe damage to proteins cause congenital cataracts, while milder variants increasing s
184 rt included 114 participants with unilateral congenital cataract who underwent cataract surgery betwe
185 d records of children less than 2 years with congenital cataract who underwent primary IOL implantati
186 linical trial of 114 infants with unilateral congenital cataract who were aged 1 to 6 months at surge
187                  The only family member with congenital cataracts who did not develop glaucoma had de
188 ession recognition, we studied children with congenital cataracts who have undergone sight-correcting
189  skill in three groups: patients treated for congenital cataracts whose pretreatment visual acuity wa
190 1 of 12 family members (7 male [63.6%]) with congenital cataract with a mean (SD) follow-up of 30 (21
191                                  In cases of congenital cataract with concomitant intraocular inflamm
192  The mean cost of treatment for a unilateral congenital cataract with primary IOL implantation was $1
193 ngs suggest that the molecular basis for the congenital cataract with the alpha A-R116C mutation is d
194 ngs suggest that the molecular basis for the congenital cataract with the alphaA-R116C mutation is th
195 reaction to probe for spiroplasma species in congenital cataracts with an inflammatory component.
196 ave been reported to date, all presenting as congenital cataracts with concomitant intraocular inflam
197  visual experience), individuals treated for congenital cataracts years after birth (late visual expe

 
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