Seckel syndrome accompanied by semilobar holoprosencephaly and arthrogryposis.

@article{Sarici2012SeckelSA,
  title={Seckel syndrome accompanied by semilobar holoprosencephaly and arthrogryposis.},
  author={Dilek Sarici and Mustafa Ali Akin and Ahu Kara and Selim Doğanay and Selim Kurtoğlu},
  journal={Pediatric neurology},
  year={2012},
  volume={46 3},
  pages={189-91}
}
Seckel syndrome is a rare autosomal recessive disorder, and its characteristic features include prenatal and postnatal growth retardation, microcephaly, and "bird-like" face with prominent, beak-like nose and micrognathia. Additional abnormalities were described in the cardiovascular, hematopoietic, endocrine, and central nervous systems. We present the… CONTINUE READING