» Articles » PMID: 33073167

Prenatal Diagnosis of FATCO Syndrome (Fibular Aplasia, Tibial Campomelia, and Oligosyndactyly) with 2D/3D Ultrasonography

Overview
Publisher Thieme
Date 2020 Oct 19
PMID 33073167
Citations 2
Authors
Affiliations
Soon will be listed here.
Citing Articles

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.

Deftereou T, Karapepera V, Alexiadi C, Tologkos S, Papadatou V, Alexiadis G Cureus. 2024; 16(7):e65162.

PMID: 39176338 PMC: 11339580. DOI: 10.7759/cureus.65162.


New pathogenic variant in : New clues for a clinical spectrum from split-hand-foot malformation to fibular aplasia, tibial campomelia and oligosyndactyly.

Sifre-Ruiz A, Sagasta A, Santos E, Perez de Nanclares G, Heath K Front Genet. 2023; 14:1165780.

PMID: 37124614 PMC: 10133553. DOI: 10.3389/fgene.2023.1165780.

References
1.
Huber J, Volpon J, Ramos E . Fuhrmann syndrome: two Brazilian cases. Clin Dysmorphol. 2003; 12(2):85-8. DOI: 10.1097/00019605-200304000-00002. View

2.
Bieganski T, Jamsheer A, Sowinska A, Baranska D, Niedzielski K, Kozlowski K . Three new patients with FATCO: fibular agenesis with ectrodactyly. Am J Med Genet A. 2012; 158A(7):1542-50. DOI: 10.1002/ajmg.a.35369. View

3.
Sezer O, Gebesoglu I, Yuan B, Karaca E, Gokce E, Gunes S . Fibular aplasia, tibial campomelia, and oligosyndactyly: a further patient with a 2-year follow-up. Clin Dysmorphol. 2014; 23(4):121-6. DOI: 10.1097/MCD.0000000000000051. View

4.
Capece G, Fasolino A, Della Monica M, Lonardo F, Scarano G, Neri G . Prenatal diagnosis of femur-fibula-ulna complex by ultrasonography in a male fetus at 24 weeks of gestation. Prenat Diagn. 1994; 14(6):502-5. DOI: 10.1002/pd.1970140616. View

5.
Eze K, Akhigbe A, Awosanya G . Fibular hemimelia: a case report. Niger J Clin Pract. 2007; 10(3):259-61. View