Fronto-Orbital Advance in a Patient With Roberts Syndrome
| Autor: | Jesus Andres Duque Montealegre, Carlos Perez Cataño, Jaime Andres Jimenez Alvarez, José Manuel Valdés Reyes, Leonardo Andres Chacon |
|---|---|
| Rok vydání: | 2020 |
| Předmět: |
Pediatrics
medicine.medical_specialty Ectromelia Craniosynostosis Craniofacial Abnormalities Craniosynostoses 03 medical and health sciences 0302 clinical medicine Female patient medicine Humans Rare syndrome natural sciences Roberts syndrome 030223 otorhinolaryngology Survival rate health care economics and organizations Coronal craniosynostosis Hypertelorism business.industry Infant social sciences 030206 dentistry General Medicine Plastic Surgery Procedures medicine.disease humanities Otorhinolaryngology Frontal Bone Female Surgery business Orbit Brachycephaly Rare disease |
| Zdroj: | Journal of Craniofacial Surgery. 31:e574-e577 |
| ISSN: | 1536-3732 1049-2275 |
| Popis: | Roberts Syndrome is an extremely rare syndrome reporting about 150 cases in the literature, with a very low survival rate. The authors present a case of a female patient with Roberts Syndrome who also had a coronal craniosynostosis. The aim of this case report is to present a case of a patient with Roberts Syndrome with a brachycephaly that required management of fronto-orbital advancement. In conclusion Roberts Syndrome is a rare disease, which can have different skeletal variations. This syndrome can manifest itself with craniosynostosis, with the requirement of a comprehensive management to correct it and avoid compression of the brain with endocranial hypertension. |
| Databáze: | OpenAIRE |
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