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Updated: Aug 27, 2025

Quantification of Orofacial Phenotypes in Xenopus
Published on: November 6, 2014
Orofacial Deformities in 3 Related Rhesus Monkeys (Macaca mulatta) Resembling Human Binder's Syndrome
Beatriz Goldschmidt1, Aline C Bouzon1, Bárbara C S Meireles1
1Department of Primatology, Institute of Science and Technology in Biomodels, Oswaldo Cruz Foundation, Rio de Janeiro, Brazil.
Researchers present a primate biomodel for Binder phenotype, a rare congenital midface hypoplasia. This study explores orofacial deformities in rhesus monkeys, linking them to potential vitamin K metabolism interference.
Area of Science:
- Genetics
- Developmental Biology
- Primate Models
Background:
- Binder's syndrome is a rare congenital condition causing midface hypoplasia.
- Etiology is often linked to genetic factors or prenatal teratogen exposure.
- A primate model is lacking for studying this condition.
Purpose of the Study:
- To present a novel primate biomodel for Binder's syndrome.
- To describe orofacial deformities in rhesus monkeys resembling the human condition.
- To investigate potential contributing factors, including vitamin K metabolism.
Main Methods:
- Clinical observation and description of three related rhesus monkeys.
- Comparison of orofacial deformities with human Binder phenotype cases.
- Discussion of management and environmental factors.
Main Results:
- Three related rhesus monkeys exhibited orofacial deformities similar to Binder phenotype.
- This represents the first primate biomodel for this condition.
- Findings suggest a potential link between vitamin K metabolism and Binder's syndrome.
Conclusions:
- A rhesus monkey model offers a new avenue for studying Binder's syndrome.
- Environmental and metabolic factors, such as vitamin K, may play a role in its development.
- Further research is warranted to elucidate the precise mechanisms involved.
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