10 top medical experts on Type 1 Kenny-Caffey syndrome across 2 countries and 2 U.S. states. This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Type 1 Kenny-Caffey syndrome: A rare, primary bone dysplasia characterized by prenatal and postnatal growth retardation, short stature, cortical thickening and medullary stenosis of the long bones, absent diploic space in the skull bones, hypocalcemia due to the hypoparathyroidism, small hands and feet, delayed mental and motor development, intellectual disability, dental anomalies, and dysmorphic features, including prominent forehead, small deep-set eyes, beaked nose, and micrognathia.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: Kenny Caffey syndrome,  Kenny syndrome,  Autosomal Recessive Kenny-Caffey Syndrome,  autosomal recessive form Kenny-Caffey syndrome


  

        

                    


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