Mutations in IFT80 cause SRPS Type IV. Report of two families and review.

Varoona BizaouiCéline HuberEva KohautJoelle RoumeMaryse BonnièreTania Attié-BitachValérie Cormier-Daire
Published in: American journal of medical genetics. Part A (2019)
We report novel causative mutations in the IFT80 gene identified in four fetuses from two unrelated families with Beemer-Langer syndrome (BLS) or BLS-like phenotypes. We discuss the implication of the IFT80 gene in ciliopathies, and its diagnostic value for BLS among other SRPS.