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Dergiler / EurAsian Journal of Oral and Maxillofacial Surgery / 2026 / Volume: 4 Issue: 1

Zimmermann-Laband Syndrome: Vaka Raporu

Zimmermann-Laband Syndrome: A Case Report

Gürkan Raşit Bayar(UNIVERSITY OF KYRENIA, FACULTY OF DENTISTRY)0000-0003-4119-9629
Kerim Ortakoğlu(Pırıl Dent İmplant Merkezi)0009-0009-4325-7061
H. Aykut Özyiğit(UNIVERSITY OF KYRENIA, FACULTY OF DENTISTRY)0009-0007-8488-6564
Sayfa
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Yayın Tarihi
2025-01-29
DOI
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Yapay Zeka Hızlı Bakış & Çıkarımlar

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⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

Ek bulgular arasında doğuştan gelen kıvrımlı parmaklar ve anterior open-bite yer alıyordu.

📌 3 Maddede Bu Makale

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Amaç & Hipotez:Zimmerman-Laband Sendromu (ZLS), gingival fibromatozis, kraniofasiyal anormaliler ve uzuv deformiteleri ile karakterize edilen nadir bir genetik hastalıktır.
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Temel Bulgular & Veri:Bu vaka raporu, ZLS'nin klasik ve özgün özellikleriyle başvuran 21 yaşında bir erkek hastayı tanımlamaktadır.
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Sonuç & Katkı:Ek bulgular arasında doğuştan gelen kıvrımlı parmaklar ve anterior open-bite yer alıyordu.
🔬Tür:Case Report
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Zimmerman-Laband syndrome · gingival fibromatosis · anterior open bite

Özet

Zimmerman-Laband Sendromu (ZLS), gingival fibromatozis, kraniofasiyal anormaliler ve uzuv deformiteleri ile karakterize edilen nadir bir genetik hastalıktır. Bu vaka raporu, ZLS'nin klasik ve özgün özellikleriyle başvuran 21 yaşında bir erkek hastayı tanımlamaktadır. Hasta, anterior dişlerin sürmemesi nedeniyle sevk edilmiştir. Klinik muayene, gingival fibromatozsiz, hipoplastik tırnaklar ve geniş, düz bir burun ile uyumluydu. Ek bulgular arasında doğuştan gelen kıvrımlı parmaklar ve anterior open-bite yer alıyordu. Radyografik değerlendirme, birden fazla gömülü ve süpernümerer dişi ortaya koymuştur. Hastanın çürük ve süpernümerer dişleri çekilmiştir. Sürmeyen dişler ve anterior open-bite için ortodontik ve cerrahi müdahaleler planlanmıştır. Bu rapor, ZLS'nin fenotipik spektrumunu genişleterek, daha önce bildirilmeyen kıvrımlı parmaklar ve çekiç parmaklar gibi bulguları tanımlamaktadır. ZLS hastalarında sonuçların iyileştirilmesi için kapsamlı bir değerlendirme ve multidisipliner yaklaşım gereklidir.

Abstract

Zimmerman-Laband Syndrome (ZLS) is a rare genetic disorder characterized by gingival fibromatosis, craniofacial abnormalities, and limb deformities. This case report describes a 21-year-old male presenting with classical and unique features of ZLS. A male patient was referred for failure of anterior teeth eruption. Clinical examination revealed gingival fibromatosis, hypoplastic toenails, and a broad, flat nose. Additional findings included congenital curly toes and an anterior open bite. Radiographic evaluation identified multiple impacted and supernumerary teeth. The patient underwent extraction of carious and supernumerary teeth. Orthodontic and surgical interventions were planned for managing unerupted teeth and anterior open bite. This report expands the phenotypic spectrum of ZLS, describing previously unreported findings such as curly toes and hammer toes. Comprehensive evaluation and interdisciplinary management are essential for optimizing outcomes in ZLS patients.

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Bu Makaleye Atıf Yap

Bayar, G. R., Ortakoğlu, K., Özyiğit, H. A. (2025). Zimmermann-Laband Syndrome: Vaka Raporu. EurAsian Journal of Oral and Maxillofacial Surgery, Volume: 4 Issue: 1. https://ajindex.com/articles/1629634

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