1962
DOI: 10.1177/003591576205501222
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The Oral Changes in Gargoylism

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Cited by 19 publications
(14 citation statements)
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“…More than one third of our group of patients demonstrated delayed dental development and eruption despite the absence of gingival hypertrophy. It would seem, therefore, that gingival hypertrophy is unlikely to be the primary cause of the delayed dental development in Hurler Syndrome as previously thought 15 . While a small minority of patients had minimal GVHD of the skin, no patients experienced GVHD of the gut or oral cavity.…”
Section: Discussionmentioning
confidence: 73%
See 1 more Smart Citation
“…More than one third of our group of patients demonstrated delayed dental development and eruption despite the absence of gingival hypertrophy. It would seem, therefore, that gingival hypertrophy is unlikely to be the primary cause of the delayed dental development in Hurler Syndrome as previously thought 15 . While a small minority of patients had minimal GVHD of the skin, no patients experienced GVHD of the gut or oral cavity.…”
Section: Discussionmentioning
confidence: 73%
“…It would seem, therefore, that gingival hypertrophy is unlikely to be the primary cause of the delayed dental development in Hurler Syndrome as previously thought. 15 While a small minority of patients had minimal GVHD of the skin, no patients experienced GVHD of the gut or oral cavity. This is not surprising as all patients had fully matched grafts.…”
Section: Discussionmentioning
confidence: 99%
“…Therefore, clinicians should be prompted to establish definitive rules regarding the relation between MPS and this kind of impaction conditions. Cawson [ 10 ] reported a patient affected with MPS and suggested that MPS could be a possible aetiological factor for occurrence of kissing molars. Also, Nakamura et al [ 11 ] reported multiple rosetting of molars in their 2 out of 4 patients with MPS.…”
Section: Discussionmentioning
confidence: 99%
“…13 KMs terimi literatürde mukopolisakkaridoz (MPS) ile ilişkilendirilmiştir. 8,12,18 Kalıtsal metabolik bozukluk ve enzim anormalliği ile karakterize bir rahatsızlık olan MPS; kornea, kalp, karaciğer, santral sinir sistemi, kemik ve diğer bölgelerde anormal mukopolisakkarit birikimine yol açar. 19 MPS'nin en yaygın klinik özellikleri, kısa boy, makrosefali, kaba yüz, anormal saçlar, belirgin frontal çıkıntılar, kornea bulanıklaşması, geniş burun ucuyla deprese burun köprüsü, dolu yanaklar, genişlemiş dudaklar, uzun düzleşmiş bir filtrum ile sertleşmiş torasik kafes ve J-şekilli sella tursikadır.…”
Section: Türkiye Klinikleri Diş Hekimliği Bilimleri Dergisiunclassified