Fatco syndrome is a syndrome consisting of
- fibular aplasia
- tibial campomelia and
It is a syndrome of unknown genetic basis and inheritance with variable expressivity and penetrance.
- 1. Courtens W, Jespers A, Harrewijn I, Puylaert D, Vanhoenacker F. Fibular aplasia, tibial campomelia, and oligosyndactyly in a male newborn infant: a case report and review of the literature. American journal of medical genetics Part A. 2005;134(3):321–25. [PubMed]
- 2. Kitaoka T, Namba N, Kim JY, Kubota T, Miura K, Miyoshi Y, et al. A Japanese male patient with ‘fibular aplasia, tibial campomelia and oligodactyly’: an additional case report. Clinical pediatric endocrinology : case reports and clinical investigations. official journal of the Japanese Society for Pediatric Endocrinology. 2009;18(3):81–86. [PMC free article] [PubMed]