ライフサイエンスコーパス: ptosis

1 ocomotion, grooming, diarrhea, tachypnea and ptosis.

2 e use of frontalis suspension for correcting ptosis.

3 ive ophthalmoplegia, often with accompanying ptosis.

4 al mortality, scoliosis, resting tremors and ptosis.

5 ve paralytic ophthalmoplegia with or without ptosis.

6 ds and feet, scoliosis, ophthalmoplegia, and ptosis.

7 in vivo by reversal of tetrabenazine-induced ptosis.

8 nonproptotic ophthalmoplegia with or without ptosis.

9 at a tertiary medical center for congenital ptosis.

10 y sympathetic nervous system defects causing ptosis.

11 episodes of facial hypotonia, jaw drop, and ptosis.

12 a levator advancement was required to repair ptosis.

13 0 (18.7%) of the 107 patients with childhood ptosis.

14 with distinctive facial features, including ptosis.

15 6 (14.9%) of the 107 patients with childhood ptosis.

16 were less likely to have postoperative brow ptosis.

17 cell proliferation, differentiation, and apo ptosis.

18 tions and new proposals in the management of ptosis.

19 ures, 5 (11%) permanent and 4 (9%) transient ptosis, 5 (11%) thermoregulation difficulties, 4 (9%) a

20 epicanthic folds (84%), hypertelorism (68%), ptosis (56%), high upper eyelid crease (64%), lower eyel

21 retro-orbital pain and later with diplopia, ptosis, 6th nerve and pupil-sparing partial 3rd nerve pa

22 diplopia, abnormal eyelid signs (retraction, ptosis, absent crease), ocular asymmetry (hypoglobus, en

23 lar muscles (CFEOM1) are born with bilateral ptosis and a restrictive infraductive external ophthalmo

24 form neurofibromas, most commonly because of ptosis and anisometropia.

25 ome but that some specific features, such as ptosis and blepharophimosis, are mostly driven by BRPF1

26 rgeons have made a change in the delivery of ptosis and blepharoplasty surgical services after the re

27 ia eliminates needle risk as well as risk of ptosis and bruising.

28 Ptosis and diplopia developed in 2 patients despite Medp

29 er of late onset that commonly presents with ptosis and dysphagia.

30 Eighteen months post initial presentation ptosis and eye movements returned normal and choroidal e

31 ngestion, 46% conjunctival injection and 40% ptosis and facial flushing.

32 tion, 58% rhinorrhoea, 54% nasal congestion, ptosis and facial flushing.

33 (9.9%) were diagnosed with simple congenital ptosis and had strabismus, of which there were 4 (4.9%)

34 he 10-year results of surgery for congenital ptosis and identify factors associated with excellent ou

35 vances in the anatomic understanding of brow ptosis and in the procedures used to correct the resulti

36 nority of individuals have been upper eyelid ptosis and midline dermoid cysts of craniofacial structu

37 cally characterized by exercise intolerance, ptosis and muscle weakness.

38 Patients with severe ptosis and nearly total absence of levator muscle functi

39 months, with little or no facial weakness or ptosis and no ophthalmoplegia.

40 rom retrochiasmal visual pathway damage, and ptosis and ocular dysmotility from extraocular muscle in

41 sarthria, gross motor regression, hypotonia, ptosis and ophthalmoplegia and had abnormal signals in b

42 of classic myasthenic manifestations such as ptosis and ophthalmoplegia or facial weakness, and links

43 spiratory and generalized limb weakness with ptosis and ophthalmoplegia.

44 a late-onset ocular myopathy beginning with ptosis and progressing slowly.

45 utosomal recessive disorder characterized by ptosis and progressive external ophthalmoplegia, periphe

46 in the fifth or sixth decade with dysphagia, ptosis and proximal limb weakness.

47 in the fifth or sixth decade with dysphagia, ptosis and proximal limb weakness.

48 dure, a historical knowledge of involutional ptosis and ptosis repair is necessary.

49 CFEOM presents with congenital ptosis and restricted eye movements, and can be caused b

50 Affected individuals are born with bilateral ptosis and restrictive ophthalmoplegia with the globes "

51 either progressive external ophthalmoplegia/ptosis and spastic ataxia, or a progressive ataxic disor

52 patients in this case series documented mild ptosis and striking orthostatic reductions in intraocula

53 surgical options depends on the cause of the ptosis and the amount of levator function.

54 A man in his late 60s had ptosis and tremor on standing for 30 years, followed by

55 amblyopia who were diagnosed with childhood ptosis and were residents of Olmsted County, Minnesota,

56 -five percent (15 of 23) of our patients had ptosis and/or diplopia, each present in 11 individuals.

57 gical data, indication for surgery, previous ptosis and/or eyelid surgeries and trauma histories, pre

58 ial nerve branches, which can result in brow ptosis and/or orbicularis oculi weakness.

59 cular muscles and results in droopy eyelids (ptosis) and progressive external ophthalmoplegia.

60 cular muscles and results in droopy eyelids (ptosis) and progressive external ophthalmoplegia.

61 10 patients diagnosed with simple congenital ptosis, and a predominance of isolated horizontal deviat

62 se the unusual combination of optic atrophy, ptosis, and encephalomyopathy leading to intractable sei

63 physical appearance secondary to proptosis, ptosis, and facial disfigurement, leading to social emba

64 We studied a woman who presented with PEO, ptosis, and weakness of pharyngeal, facial, neck, and li

65 lasia, decreased innervation of the gut, and ptosis are consistent with impaired Ret signaling.

66 ture on the classification and management of ptosis are reviewed here.

67 options for correction of specific types of ptosis are reviewed.

68 The treatment options for ptosis are strictly surgical.

69 ren who were diagnosed with childhood eyelid ptosis as residents of Olmsted County, Minnesota, from J

70 ble, the simultaneous onset of OT and eyelid ptosis at a much younger age than usually observed for O

71 elta translocates to mitochondria during apo-ptosis,but its mitochondrial target remains unclear.

72 Bilateral ptosis cases with documented Hering's dependency yield b

73 The attacks were associated with ipsilateral ptosis, conjunctival injection, lacrimation, rhinorrhoea

74 gle exotropia, vertical gaze deficiency, and ptosis consistent with congenital fibrosis of the extrao

75 patients diagnosed with a congenital form of ptosis demonstrated amblyopia.

76 After pterional craniotomy, ptosis, diplopia, and vertical gaze limitation can resul

77 ith exotropia, vertical gaze limitation, and ptosis do not have classic Moebius syndrome and may have

78 with the classical features of OPMD, namely ptosis, dysphagia and cytoplasmic inclusions on muscle b

79 is an adult-onset disorder characterized by ptosis, dysphagia and proximal limb weakness.

80 minant disorder characterized by progressive ptosis, dysphagia, and extremity weakness.

81 of acute cranial nerve dysfunction including ptosis, dysphagia, blurred vision, and motor weakness.

82 Blepharophimosis, ptosis, epicanthus inversus syndrome (BPES) is an autoso

83 Blepharophimosis, ptosis, epicanthus inversus syndrome type I (BPES; OMIM

84 the lacrimal gland (LG) in blepharophimosis-ptosis-epicanthus inversus syndrome (BPES).

85 phology in both sexes (the 'blepharophimosis-ptosis-epicanthus inversus syndrome', BPES).

86 eon and reviewed in detail: blepharophimosis-ptosis-epicanthus inversus syndrome, congenital fibrosis

87 tion disorders--a subset of blepharophimosis-ptosis-epicanthus inversus syndrome, Miller-Dieker lisse

88 ranscription factor, causes blepharophimosis/ptosis/epicanthus inversus syndrome (BPES), a rare devel

89 xL2 are associated with the blepharophimosis/ptosis/epicanthus inversus syndrome characterized with c

90 the literature and in this patient, included ptosis, esotropia, coloboma of the iris, retina, choroid

91 All patients underwent standard preoperative ptosis evaluation with margin-to-reflex distance 1 and 2

92 tonomic dysfunction in children undergoing a ptosis evaluation.

93 sh a map location for an isolated congenital ptosis gene and demonstrate that this disorder is geneti

94 omal-dominant form of mild syndromic ID with ptosis, growth retardation, and hypotonia, and we identi

95 Surgical treatment of congenital ptosis had a high success rate.

96 81 patients diagnosed with simple congenital ptosis had amblyopia, 7 (8.6%) cases of which solely wer

97 Those patients with a history of ptosis had undergone surgery with levator procedure at l

98 Four patients had traumatic ptosis history whereas four patients had previous multip

99 aly, low frontal hairline, facial asymmetry, ptosis, hypertelorism, broad great toes, and clinodactyl

100 Seven patients had ptosis in the left eye whereas one patient had ptosis in

101 osis in the left eye whereas one patient had ptosis in the right eye.

102 hildren diagnosed with any form of childhood ptosis in this population-based cohort.

103 a occurred in 1 in 7 children diagnosed with ptosis in this population-based cohort.

104 d sickness behavior (lethargy, piloerection, ptosis) in the GR(dim)-LPS mice was associated with incr

105 rome (KOS, also reported as blepharophimosis-ptosis-intellectual disability syndrome).

106 Hereditary isolated congenital ptosis is an autosomal dominant disorder with incomplete

107 geons have increasingly recognized that brow ptosis is an important contributor to dermatochalasis an

108 Bilateral ptosis is reported with unilateral hemispheric lesions,

109 ain, pain in the arm used for drug infusion, ptosis, leg cramps, and visual and voice changes.

110 The cardinal features were ptosis, limited elevation, and hypotropia.

111 Automated ptosis measurements produced by our software algorithm c

112 well as skeletal and eye abnormalities (ie, ptosis, myopia, and retina detachment).

113 d by strabismus (n = 2, 10%), occlusion from ptosis (n = 9, 43%), or anisometropia (n = 9, 43%), or a

114 cus often have atypical phenotypes including ptosis, obstructive sleep apnoea, and the occurrence of

115 ealed marked periorbital edema and hematoma, ptosis, ocular movements limitation, an infero-temporal

116 important contributor to dermatochalasis and ptosis of the upper eyelid.

117 rns-Sayre syndrome consisting of progressive ptosis, ophthalmoparesis, mitochondrial myopathy, and pi

118 vere gastrointestinal dysmotility; cachexia; ptosis, ophthalmoparesis, or both; peripheral neuropathy

119 report describes monozygotic male twins with ptosis, optic atrophy, and recent-onset intractable myoc

120 lacrimation, nasal congestion, rhinorrhoea, ptosis or eyelid oedema.

121 surgery for cataract, strabismus, nystagmus, ptosis, or nasolacrimal duct obstruction.

122 regulator of the TNF-alpha-mediated anti-apo-ptosis pathways in RA FLSs.

123 ons, and innovative materials in the care of ptosis patients.

124 teral optic neuropathy, ophthalmoplegia with ptosis, pigmentary retinopathy, and retrochiasmal visual

125 abnormal signs in the animals: for example, ptosis, piloerection, tremor, ataxia or exophthalmos.

126 isystem disorder characterized clinically by ptosis, progressive external ophthalmoplegia, gastrointe

127 onset typically before the age of 30 years; ptosis; progressive external ophthalmoplegia; gastrointe

128 nt are variable and include eyelid swelling, ptosis, proptosis, and loss of vision.

129 ber of patients in Group 1 had mild residual ptosis, proptosis, and movement restriction at 12 weeks,

130 h of hospital stay, and sequelae of disease (ptosis, proptosis, and movement restriction) were evalua

131 utures, inflammation, granuloma formation or ptosis recurrence, were registered.

132 atients undergo separate surgical visits for ptosis repair and blepharoplasty, is not desirable to mo

133 d 2 are crucial for the surgical planning of ptosis repair and blepharoplasty.

134 to examine the history of posterior approach ptosis repair and the events that have led to its curren

135 the MMCR, and the current reimbursements for ptosis repair by insurance companies.

136 Posterior approach ptosis repair has made a resurgence over the last decade

137 torical knowledge of involutional ptosis and ptosis repair is necessary.

138 ty or having to wait at least 3 months after ptosis repair to have a blepharoplasty.

139 important adjuncts for adult and congenital ptosis repair.

140 d in two favored techniques for involutional ptosis repair: the Muller muscle-conjunctiva resection (

141 There are certain established surgeries in ptosis repair; however, there is no ideal surgical techn

142 g the etiology and appropriate management of ptosis requires a directed evaluation seeking specific s

143 onally, all mutation carriers had congenital ptosis requiring surgery, 4 had myopia, 2 had retinal de

144 ngenital disorder characterized by bilateral ptosis, restrictive external ophthalmoplegia with the ey

145 gait ataxia, scoliosis, resting tremors, and ptosis, suggesting a defect in proprioception.

146 ution of the posterior and anterior approach ptosis surgeries has resulted in two favored techniques

147 f patients who underwent levator advancement ptosis surgery between April 2002 and December 2004 by t

148 c changes in adult patients following eyelid ptosis surgery is 1 year and a considerable number of pa

149 tear production is recommended especially if ptosis surgery is planned.

150 rithm showing the appropriate/most preferred ptosis surgery techniques is prepared based on the tradi

151 The recent preference for posterior approach ptosis surgery, in particular the MMCR, is multifactoria

152 late-onset muscle disorder characterized by ptosis, swallowing difficulties, proximal limb weakness

153 fering opinions on the cause of involutional ptosis, the mechanism by which the MMCR works, the predi

154 t hemispheric infarctions, in whom bilateral ptosis was accompanied by impaired upward gaze.

155 both ocular and pharyngeal muscle weakness, ptosis was just as likely to occur before or concurrent

156 'limb-girdle' pattern of weakness; although ptosis was often present from an early age, eye movement

157 Ptosis was the first reported symptom in two-thirds of t

158 Induction of apo-ptosis which causes the insertion of the soluble form of

159 y-three patients diagnosed with involutional ptosis who underwent surgical correction using a small o

160 blepharoptosis, used widely in the repair of ptosis with poor levator function.