A Multicenter Clinical Analysis of Cleft Lip and Palate: Clinical Features, Parental Background, and Associated Anomalies

ObjectiveTo provide a contemporary, multicenter clinical and epidemiologic overview of cleft lip and/or palate (CL/P) and to analyze associations with phenotype, Veau classification, parental characteristics, and perinatal factors.MethodsThis retrospective multicenter study included 2488 patients with CL/P treated between 2018 and 2022 at 11 tertiary referral centers in Türkiye. Demographic data, cleft phenotype, Veau classification, syndromic status, associated congenital anomalies, parental age, consanguinity, antenatal follow-up, teratogenic exposure, and perinatal complications were analyzed using descriptive and comparative statistics.ResultsA total of 2488 patients with CL/P were included. Combined cleft lip and palate (CLP) was the most common phenotype (44.8%), followed by cleft palate (CP only-34.3%) and cleft lip (CL only-20.9%). Syndromic or sequential conditions were present in 5.7% and associated congenital anomalies in 17.0%, most frequently cardiovascular defects (7.0%). Consanguinity was reported in 21.9% of families. Compared with CL and CLP, CP was characterized by female predominance and significantly higher rates of syndromic involvement, associated anomalies, and perinatal complications. These associations remained significant in multivariable analysis. Among patients with CP, incomplete CP (Veau I-II) was independently associated with female sex, syndromic status, and perinatal complications. Higher maternal and paternal ages were associated with nonpreterm perinatal complications but not with preterm birth.ConclusionsCP only represents a distinct clinical and epidemiologic entity with a higher syndromic and comorbidity burden. This large multicenter cohort provides updated reference data for contemporary cleft research and supports subtype-specific evaluation and multidisciplinary management.Level of evidenceLevel III-Prognostic/Etiologic Evidence (Retrospective Cohort Study).

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Journal
The Cleft Palate-Craniofacial Journal
Published
2026-07-22
DOI
https://doi.org/10.1177/10556656261464302
Primary Topic
Cleft Lip and Palate Research
Type
article
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article

A Multicenter Clinical Analysis of Cleft Lip and Palate: Clinical Features, Parental Background, and Associated Anomalies

Tahir Gürler, Galip Gencay Üstün, Mert Çalış, Kutluhan Yusuf Küçük et al.
The Cleft Palate-Craniofacial Journal
Cleft Lip and Palate Research
article

A Multicenter Clinical Analysis of Cleft Lip and Palate: Clinical Features, Parental Background, and Associated Anomalies

Tahir Gürler, Galip Gencay Üstün, Mert Çalış, Kutluhan Yusuf Küçük, Mert Doruk, Şeyhmus Mete, Mehmet Kara, Göktekin Tenekeci, Erol Kesiktaş, Güven Ozan Kaplan, Mehmet Dadacı, Serhat Şibar, Osman Enver Aydın, Ender Ceylan, İbrahim Tabakan, Ahmet Demir, Şeyda Güray, Yusuf Irmak, Figen Özgür, Ahmet Koyuncu, Şakir Ünal, ÇAĞLA ÇİÇEK, Gaye Filinte, Dicle Aksöyler, Osman Dağ, Murat Deha Uruç, Bartu Yiğit Çalık, Ahmet Said Doğruyol, Ahmet Biçer
article en

Abstract

ObjectiveTo provide a contemporary, multicenter clinical and epidemiologic overview of cleft lip and/or palate (CL/P) and to analyze associations with phenotype, Veau classification, parental characteristics, and perinatal factors.MethodsThis retrospective multicenter study included 2488 patients with CL/P treated between 2018 and 2022 at 11 tertiary referral centers in Türkiye. Demographic data, cleft phenotype, Veau classification, syndromic status, associated congenital anomalies, parental age, consanguinity, antenatal follow-up, teratogenic exposure, and perinatal complications were analyzed using descriptive and comparative statistics.ResultsA total of 2488 patients with CL/P were included. Combined cleft lip and palate (CLP) was the most common phenotype (44.8%), followed by cleft palate (CP only-34.3%) and cleft lip (CL only-20.9%). Syndromic or sequential conditions were present in 5.7% and associated congenital anomalies in 17.0%, most frequently cardiovascular defects (7.0%). Consanguinity was reported in 21.9% of families. Compared with CL and CLP, CP was characterized by female predominance and significantly higher rates of syndromic involvement, associated anomalies, and perinatal complications. These associations remained significant in multivariable analysis. Among patients with CP, incomplete CP (Veau I-II) was independently associated with female sex, syndromic status, and perinatal complications. Higher maternal and paternal ages were associated with nonpreterm perinatal complications but not with preterm birth.ConclusionsCP only represents a distinct clinical and epidemiologic entity with a higher syndromic and comorbidity burden. This large multicenter cohort provides updated reference data for contemporary cleft research and supports subtype-specific evaluation and multidisciplinary management.Level of evidenceLevel III-Prognostic/Etiologic Evidence (Retrospective Cohort Study).

The Cleft Palate-Craniofacial Journal
Ondokuz Mayıs University (TR), Ege University (TR), Dr Lütfi Kırdar Kartal Eğitim ve Araştırma Hastanesi (TR), Necmettin Erbakan University (TR), Mersin Üniversitesi (TR), Cukurova University (TR), Hacettepe University (TR), Istanbul University (TR), Marmara University (TR), Adnan Menderes University (TR), Gazi University (TR)
Good health and well-being
Openalex Percentile: Top 8%
Cleft Lip and Palate Research
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