Maternal vitamin K deficient embryopathy: association with hyperemesis gravidarum and Crohn disease.

@article{Toriello2013MaternalVK,
  title={Maternal vitamin K deficient embryopathy: association with hyperemesis gravidarum and Crohn disease.},
  author={Helga V. Toriello and Miriam Erick and J L Alessandri and Diana M. Bailey and Nicola Brunetti-Pierri and Helen E Cox and Alan Fryer and Denise Marty and Charles McCurdy and John Butler Mulliken and Helen R Murphy and Joseph Omlor and Richard M. Pauli and Judith D Ranells and Amarillis Sanchez-Valle and Ana Marie Tobiasz and Lionel Van Maldergem and Angela E. Lin},
  journal={American journal of medical genetics. Part A},
  year={2013},
  volume={161A 3},
  pages={417-29}
}
Chondrodysplasia punctata (CDP) is an etiologically heterogeneous disorder characterized by the radiographic finding of stippled epiphyses (punctate calcifications). It is often accompanied by a characteristic facial appearance, known as the Binder phenotype, which is attributed to hypoplasia of the nasal cartilages; abnormal distal phalanges (brachytelephalangy) are a common component manifestation as well. We report eight patients with a Binder phenotype with or without CDP who all shared a… CONTINUE READING