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2018, vol. 146, br. 7-8, str. 447-451
Ankiloblefaron filiforme adnatum sa obostranim rascepom usne i nepca
aUniverzitet u Nišu, Medicinski fakultet + Klinički centar Niš, Klinika za očne bolesti
bUniverzitet u Nišu, Medicinski fakultet

e-adresagordanasb@mts.rs
Sažetak
Uvod Ankyloblepharon filiforme adnatum (AFA) retka je kongenitalna abnormalnost kapaka, saopštavana kao izolovan nalaz, udružena sa drugim anomalijama ili kao deo dobro definisanih sindroma. Cilj ovog rada je bio da prikaže bolesnika sa familijarnim AFA, udruženog sa obostranim rascepom usne i nepca. Prikaz bolesnika Terminsko novorođenče (40 nedelja GS, TM 3700 g) ženskog pola rođeno je sa obostranom delimičnom fuzijom kapaka i obostranim rascepom usne i nepca. Operativno lečenje je izvedeno pet dana posle rođenja. Majka bebe je takođe imala AFA, bez rascepa usne i nepca. Devojčica se prati od strane specijaliste plastične hirurgije, ortodoncije, oftalmologa i pedijatra. Zaključak Ovaj slučaj ukazuje na familijalno grupisanje AFA, sa ozbiljnijom formom u sledećoj generaciji. Rascep usne i nepca kod našeg bolesnika zahtevao je hirurško lečenje, oralnu i zubnu rehabilitaciju, potrebu za intenzivnom negom i redovnim praćenjem multidisciplinarnih timova.
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O članku

jezik rada: engleski
vrsta rada: prikaz slučaja
DOI: 10.2298/SARH170302199S
objavljen u SCIndeksu: 04.10.2018.

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