A Case of Fibular Aplasia-Tibial Campomelia-Oligosyndactyly (FATCO) Syndrome Associated With Split Hand/Foot Syndrome With Long Bone Deficiency (SHFLD) and Review of the Literature-Reference-Cited by-同舟云学术

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A Case of Fibular Aplasia-Tibial Campomelia-Oligosyndactyly (FATCO) Syndrome Associated With Split Hand/Foot Syndrome With Long Bone Deficiency (SHFLD) and Review of the Literature

Published:2024-07-22 Issue: Volume: Page:
ISSN:2168-8184
Container-title:Cureus
language:en
Short-container-title:

Author:

Deftereou Theodora- Eleftheria,Karapepera Vaya R,Alexiadi Christina Angelika,Tologkos Stylianos,Papadatou Vasiliki,Alexiadis Georgios,Karamanidis Dimitrios,Maria Lambropoulou

Publisher

Springer Science and Business Media LLC

Reference48 articles.

1. Prenatal diagnosis of fibular aplasia-tibial campomelia-oligosyndactyly syndrome: two case reports and review of the literature;Marinho M;J Clin Ultrasound,2021

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

3. Clinical, genetic, and molecular aspects of split-hand/foot malformation: an update;Gurrieri F;Am J Med Genet A,2013

4. Insights into the pathogenesis and treatment of split/hand foot malformation (cleft hand/foot);Guero S;J Hand Surg Eur Vol,2019

5. Insights into the pathogenesis and treatment of split/hand foot malformation (cleft hand/foot);Guero S,2019

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