A syndrome of congenital thrombocytopenia with multiple malformations and neurologic dysfunction

J Pediatr. 1983 Apr;102(4):600-2. doi: 10.1016/s0022-3476(83)80198-x.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Facial Expression
  • Female
  • Humans
  • Infant, Newborn
  • Infant, Postmature
  • Male
  • Nervous System Diseases / congenital*
  • Syndrome
  • Thrombocytopenia / congenital*
  • Thrombocytopenia / genetics