Paper Title
Treacher Collin syndrome a rare disorder in neonate with respiratory failure- A Case Report
Article Identifiers
Authors
Dr. Garima Bansal , Dr. Varughese P.V.
Keywords
TCOF 1, POLR, MFD, TCS
Abstract
Treacher Collins Syndrome is a rare genetic disorder in which first and second pharyngeal arch is affected leading to disfigurement of face. These children generally have normal development but a major social stigma due to facial changes.[1,2] This is a case report of neonate born with facial deformities sparing the rest of body parts with respiratory failure. He was managed symptomatically as well as multiple teams were involved for correction of deformities. Being a rare genetic disorder, there is a social limitation leading to delay and incomplete treatment, hence education and genetic counselling are important to reassure and correct the dysmorphism. It is important to guide the parents about this disorder for future planning.
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How To Cite (APA)
Dr. Garima Bansal & Dr. Varughese P.V. (August-2023). Treacher Collin syndrome a rare disorder in neonate with respiratory failure- A Case Report. INTERNATIONAL JOURNAL OF NOVEL RESEARCH AND DEVELOPMENT, 8(8), b472-b473. https://ijnrd.org/papers/IJNRD2308157.pdf
Issue
Volume 8 Issue 8, August-2023
Pages : b472-b473
Other Publication Details
Paper Reg. ID: IJNRD_203576
Published Paper Id: IJNRD2308157
Downloads: 000121979
Research Area: Medical Science
Country: Samana, Patiala, Punjab, India
Published Paper PDF: https://ijnrd.org/papers/IJNRD2308157.pdf
Published Paper URL: https://ijnrd.org/viewpaperforall?paper=IJNRD2308157
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This work is licensed under a Creative Commons Attribution 4.0 International License and The Open Definition
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