2004
DOI: 10.1076/ceyr.28.1.11.23491
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Refractive evaluation in children with growth defect

Abstract: Our findings emphasise the possible role of growth hormone in ocular development, and its interaction with the physiological process of emmetropization.

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Cited by 28 publications
(25 citation statements)
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“…Accordingly, optic nerve hypoplasia and pseudopapilledema, as well as reduced retinal vascularization, are all described as possible signs of GH deficiency. 8 However, our patients did not have a congenital anomaly of the eye and, on detailed ophthalmologic examination, showed only a tendency to hyperopia due to the small diameter of the globe.…”
Section: Discussionmentioning
confidence: 53%
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“…Accordingly, optic nerve hypoplasia and pseudopapilledema, as well as reduced retinal vascularization, are all described as possible signs of GH deficiency. 8 However, our patients did not have a congenital anomaly of the eye and, on detailed ophthalmologic examination, showed only a tendency to hyperopia due to the small diameter of the globe.…”
Section: Discussionmentioning
confidence: 53%
“…After 6 years of age, refraction is modified mainly by increases in axial length. 8 In an earlier clinical study of 12 untreated patients with LS, refraction examination yielded only a tendency toward hyperopia related to the small globe axis, thick lens, and steep corneal curvature. 4 These differences from normal values in the literature reflect the influence of IGF-1 on the various components of the eye.…”
Section: Discussionmentioning
confidence: 94%
“…The latter feature could be related to growth hormone deficiency, 21,22 which is proposed as the cause of the various underdevelopment features of FA. The short AL and progressive increase in lens thickness appear to have predisposed the first sibling to the development of pupillary block, but it was not clear what induced the precipitous rise in IOP.…”
Section: Discussionmentioning
confidence: 99%
“…Direct support for a causal association comes from studies of individuals who fail to produce insulin-like growth factor 1 (IGF-1) due to growth hormone (GH) deficiency. Children with GH deficiency have shorter than usual axial lengths as well as short stature 22 . Furthermore, GH supplementation in these patients, and IGF-1 supplementation in patients with Laron syndrome (dysfunction of the GH receptor), at least partially brings axial length back within the normal range, as also occurs for height 23,24 .…”
Section: Introductionmentioning
confidence: 99%