Neuropathology of Seckel syndrome in fetal stage with evidence of intrauterine developmental retardation

@article{Hori1987NeuropathologyOS,
  title={Neuropathology of Seckel syndrome in fetal stage with evidence of intrauterine developmental retardation},
  author={Akira Hori and Kimiko Tamagawa and Stefan W. Eber and M. Westmeier and Ingo Hansmann},
  journal={Acta Neuropathologica},
  year={1987},
  volume={74},
  pages={397-401}
}
Marked intrauterine developmental retardation in a fetal case of Seckel syndrome was morphologically defined in the 29th week of gestation by comparing with a large number of length-matched and age-matched controls. Telencephalic micrencephaly with reduced neuroblast production, retarded functional differentiation of the pituitary gland, and generalized hypotrophy with craniofacial stigmata were observed. 

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