MeSH 搜索器

Pierre Robin Syndrome

Congenital malformation characterized by MICROGNATHIA or RETROGNATHIA; GLOSSOPTOSIS and CLEFT PALATE. The mandibular abnormalities often result in difficulties in sucking and swallowing. The syndrome may be isolated or associated with other syndromes (e.g., ANDERSEN SYNDROME; CAMPOMELIC DYSPLASIA). Developmental mis-expression of SOX9 TRANSCRIPTION FACTOR gene on chromosome 17q and its surrounding region is associated with the syndrome.
推出的年份: 1965(1964)
副标题
树号: C05.500.460.606, C05.660.207.540.460.606, C07.320.440.606, C07.650.500.460.606, C16.131.621.207.540.460.606, C16.131.850.500.460.606
MeSH 单一 ID: D010855
进入的组:
  • Robin Syndrome, Pierre
  • Syndrome, Pierre Robin
  • Robin Sequence
  • Sequence, Robin
  • Pierre Robin's Sequence
  • Pierre Robins Sequence
  • Sequence, Pierre Robin's
  • Pierre-Robin Syndrome
  • Syndrome, Pierre-Robin
  • Glossoptosis, Micrognathia, and Cleft Palate
  • Pierre Robin Sequence
  • Sequence, Pierre Robin

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