Abstract
Özet
Ellis-van Creveld sendromu, akromegalik cücelik, displastik tırnaklar, bilateral postaxial polydactyly ve konjenital kalp hastalığı ile karakterize bir sendromdur. Otosomal resessif geçişli olan bu hastalıkta oral bulgular ise; nazolabial sulkus yokluğu, çok sayıda frenulum, konjenital diş eksiklikleri, mikrodonti ve morfolojik bozukluklar, mine bipoplazisi ile natal dişler olarak rapor edilmiştir.
Anahtar sözcükler: Ellis-van Creveld Sendromu, Ghondroektodermal displazi.
Abstract
Ellis-van Creveld syndrome is characterized by acromegalic dwarfizm, dysplastİc nails, bilateral postanal Polydactyly and congenital heart disease. It is an autosomal resesive disorder that other features within die mouth are, absence of nasolabial sulcus, multiple frenula, congenitally missing teeth, microdontia, abnormality in tooth morphology, enamel hypoplasia and natal teeth.
Key words; Ellis-van Creveld syndrome, Chondroectodermal dysplasia.
Keywords
Details
| Primary Language | Turkish |
|---|---|
| Journal Section | Case Reports |
| Authors | |
| Publication Date | June 12, 2013 |
| Published in Issue | Year 1995 Volume: 29 Issue: 2 |
Cite
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