Congenital Nasal Bones Agenesis: Report of a Rare Malformation
Author Information
Author(s): Monica Russo, Chiara Ferrecchi, Silvia Rebella, Valeria Capra, Franco Ameli, Mattia Pacetti, Maria Francesca Di Feo, Pierangela De Biasio, Cesare Arioni
Primary Institution: IRCCS Ospedale Policlinico San Martino, Genoa, Italy
Hypothesis
Congenital arhinia and hyporhinia are rare facial anomalies whose management is complex and not well-defined.
Conclusion
The case presented shows that a newborn with partial congenital arhinia can have an uncomplicated neonatal course without respiratory or feeding issues.
Supporting Evidence
- The baby showed facial abnormality with a depressed nasal bridge and narrow nostrils.
- Nasal examination confirmed patency, and the baby could breathe and suck simultaneously.
- Imaging studies revealed nasal bones agenesis and frontal dysplasia.
Takeaway
This study talks about a baby born without a complete nose, but she was healthy and didn't have trouble breathing or eating.
Methodology
The case was diagnosed through clinical examination, imaging studies including CT scans, and genetic counseling.
Limitations
The study is based on a single case report, limiting the generalizability of the findings.
Participant Demographics
A live Caucasian female infant born to a 30-year-old mother.
Digital Object Identifier (DOI)
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