Bohring-Opitz Syndrome OMIM# 605039

Facial Gestalt

Visualization generated by Face2Gene.

 

Associated Gene

• ASXL1

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Key Features

  • microcephaly
  • hypertrichosis
  • feeding difficulties
  • prominent metopic ridge
  • prominent globes
  • wrist flexion deformity

London Medical Databases (LMD):
Bohring-Opitz Syndrome OMIM# 605039

 

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