A new report under the spotlight: FATCO syndrome phenotype with an absent uvula and acyanotic congenital heart diseases in an Indian female newborn-Reference-Cited by-同舟云学术

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A new report under the spotlight: FATCO syndrome phenotype with an absent uvula and acyanotic congenital heart diseases in an Indian female newborn

Published:2024-02 Issue: Volume: Page:
ISSN:1355-1841
Container-title:Journal of Neonatal Nursing
language:en
Short-container-title:Journal of Neonatal Nursing

Author:

Thakkar U.G.,Shah K.M.,Raja Z.Z.,Aggarwal R.S.,Patel R.D.,Nigam L.A.

Publisher

Elsevier BV

Reference7 articles.

1. Why do we have a uvula? literature review and a new theory;Back;Clin. Otolaryngol. Allied Sci.,2004

2. Newborn male with fibular aplasia, tibial campomelia, and oligosyndactyly syndrome: a new case report putting the condition under spotlight;Georgeos;Cureus,2022

3. Limb deficiency syndrome in half-sibs;Hecht;Clin. Genet.,1981

4. Fibular aplasia-tibial campomelia-oligodactyly syndrome phenotype with isolated ventricular septal defect in an African Child;Peter;J Pract Cardiovasc Sci,2020

5. Difficult tracheal intubation: a retrospective study;Samsoon;Anaesthesia,1987

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