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Clinical Aspects Associated with Syndromic Forms of Orofacial Clefts in a Colombian Population

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Date 2016 Feb 6
PMID 26848196
Citations 2
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Abstract

Objectives: To present descriptive epidemiology of Orofacial Clefts and to determine the association of syndromic forms with antenatal high-risk conditions, preterm birth, and comorbidities among nested-series of cases.

Methods: A study of nested-series of cases was conducted. Frequencies of cleft type, associated congenital anomalies, syndromic, non-syndromic and multiple malformation forms, and distribution of Orofacial Clefts according to sex and affected-side were determined. Odds ratios were calculated as measures of association between syndromic forms and antenatal high-risk conditions, preterm birth and comorbidities. A total of three hundred and eleven patients with Orofacial Clefts were assessed in a 12-month period.

Results: The most frequent type of Orofacial Clefts was cleft lip and palate, this type of cleft was more frequent in males, whereas cleft palate occurred more often in females. The most common cases occurred as non-syndromic forms. Aarskog-Scott syndrome showed the highest frequency amongst syndromic forms. Hypertensive disorders in pregnancy, developmental dysplasia of the hip, central nervous diseases and respiratory failure showed significant statistical associations (p <0.05) with syndromic forms.

Conclusions: These data provide an epidemiological reference of Orofacial Clefts in Colombia. Novel associations between syndromic forms and clinical variables are determined. In order to investigate causality relationships between these variables further studies must be carried out.

Citing Articles

Maternal Metabolic Status and Orofacial Cleft Risk: A Case-Control Study in Thailand.

Pisek A, McKinney C, Muktabhant B, Pitiphat W Int Dent J. 2024; 74(6):1413-1423.

PMID: 38614877 PMC: 11551577. DOI: 10.1016/j.identj.2024.02.005.


Epigenetic implications in maternal diabetes and metabolic syndrome-associated risk of orofacial clefts.

Sun B, Reynolds K, Garland M, McMahon M, Saha S, Zhou C Birth Defects Res. 2023; 115(19):1835-1850.

PMID: 37497595 PMC: 11526419. DOI: 10.1002/bdr2.2226.

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