Prenatal diagnosis of fibular aplasia‐tibial campomelia‐oligosyndactyly syndrome: Two case reports and review of the literature-Reference-Cited by-同舟云学术

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Prenatal diagnosis of fibular aplasia‐tibial campomelia‐oligosyndactyly syndrome: Two case reports and review of the literature

Published:2020-12-16 Issue:6 Volume:49 Page:625-629
ISSN:0091-2751
Container-title:Journal of Clinical Ultrasound
language:en
Short-container-title:J Clin Ultrasound

Author:

Marinho Márcia¹^ORCID,Nunes Sara²,Lourenço Cátia¹,Melo Mónica¹,Godinho Cristina¹,Nogueira Rosete³⁴

Affiliation:

1. Department of Obstetrics and Gynecology Centro Hospitalar Vila Nova de Gaia Porto Portugal

2. Department of Obstetrics and Gynecology Centro Hospitalar de Vila Real e Trás‐os‐ Montes e Alto Douro Vila Real Portugal

3. Pathology Laboratory of CGC Genetics/Centro de Genética Clínica Porto Portugal

4. Medical School, University of Minho, and ICVS/3B's‐PT Government Associate Laboratory Guimarães Portugal

Publisher

Wiley

Subject

Radiology, Nuclear Medicine and imaging

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jcu.22969

Reference15 articles.

1. Pre- and postnatal diagnosis of limb anomalies: A series of 107 cases

2. Imaging features of lower limb malformations above the foot

3. Fibular aplasia, tibial campomelia, and oligosyndactyly in a male newborn infant: A case report and review of the literature

4. Limb deficiency syndrome in half-sibs

5. Overlap between Fibular Aplasia, Tibial Campomelia, and Oligosyndactyly and Fuhrmann's Syndromes in an Egyptian Female Infant

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. 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;Cureus;2024-07-22

2. New pathogenic variant in DLX5: New clues for a clinical spectrum from split-hand-foot malformation to fibular aplasia, tibial campomelia and oligosyndactyly;Frontiers in Genetics;2023-04-13

3. Genomic sequencing in a cohort of individuals with fibular aplasia, tibial campomelia, and oligosyndactyly (FATCO) syndrome;American Journal of Medical Genetics Part A;2023-01-06

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