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Disorders of GH in childhood is outlined in the Endotext chapter Disorders of Growth Hormone in Childhood by Murray and Clayton (132) Primary IGF-I deficiency or GH insensitivity is severe in homozygous genetic defects in genes including the GH receptor (Laron syndrome) gene, STAT-5b gene and IGF-I gene

La production soudaine et massive de nouveaux globules rouges consomme une grande quantit de potassium, ce qui peut provoquer des troubles du rythme cardiaque

[19] The gut is compromised in celiac disease, and this can cause reduced nutrient absorption, including iron absorption