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Le syndrome de Laron est une maladie congénitale caractérisée par une très petite taille associée à des taux sériques normaux ou élevés d'hormone de croissance (GH) et des taux faibles d'IGF-1 (insulin-like growth factor-1) qui n'augmentent pas après administration d'hormone de croissance exogène. La maladie a été décrite dans plus de 250 cas et est plus fréquente dans les populations juives et méditerranéennes. La maladie touche indifféremment les deux sexes. Et ces personnes semblent exemptes
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