2004
DOI: 10.1016/j.jemermed.2004.02.010
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Are one or two dangerous? camphor exposure in toddlers

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Cited by 62 publications
(35 citation statements)
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References 36 publications
(41 reference statements)
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“…Intoxication with high doses leads to damage in the liver and central nervous system. Death usually occurs with respiratory arrest (2,3). In this article, a twoyear old patient who presented with seizure after ingestion of high dose camphor is presented.…”
Section: Introductionmentioning
confidence: 99%
“…Intoxication with high doses leads to damage in the liver and central nervous system. Death usually occurs with respiratory arrest (2,3). In this article, a twoyear old patient who presented with seizure after ingestion of high dose camphor is presented.…”
Section: Introductionmentioning
confidence: 99%
“…3,26,27 Some clinicians may express caution about using a product that contains camphor because of the association between toxic ingestions and adverse events such as seizures. [28][29][30][31][32] Historical concerns over the toxicity of camphor centered on the ingestion of camphor as a liquid preparation, camphorated oil, 13,33 and a recent report of seizures was associated with ingestion of illegally sold camphor. 28 In contrast with oral ingestion, dermal exposure to camphor, as occurs when following the directions for use of VR, results in low systemic exposure.…”
Section: Discussionmentioning
confidence: 99%
“…All these compounds have been obtained from camphor, which has been described in the literature as being toxic for toddlers in doses of around 750 to 1000 mg. 51 Regarding toxicity in adults, the major cause for concern appears to be the endocrine-disrupting ability of 3-and 4-methylbenzylidene camphor derivatives, which are present in UV blockers; methylbenzylidene camphor, which resembles the synthesized camphor phenazine derivative, has been associated with weak estrogenic effects on the reproductive system in rats and with a high inhibition of the pituitarythyroid hormone system, but its ability to bind the estrogen receptor type a appears to be lower than that of other phytoestrogens and xenoestrogens such as genistein, resveratrol, bisphenol A and camphor itself. [52][53][54][55] The synthesized Cl-OH derivative, with an ortho-hydroxyimine-one moiety, could possibly interact with DNA due to the presence of these two groups, but the fact that they are substituents of a bicyclic ring and not of a planar ring is likely to signicantly diminish the importance of this toxic pathway.…”
Section: Biological Assaymentioning
confidence: 99%