It is feasible that the primary title of the record Kenny-Caffey Syndrome is not the name you anticipated. Kindly inspect the words specifying to locate the alternative name(s) and also problem community(s) covered by this record.
- dwarfism, cortical thickening of tubular bones & short-term hypocalcemia
- Kenny-Caffey disorder, leading kind
Kenny-Caffey disorder kind 2 (KCS2) is an incredibly uncommon genetic skeletal problem defined by thickening of the lengthy bones, slim marrow dental caries in the bones (medullary constriction), and also irregularities impacting the head as well as eyes. The main result of KCS2 is brief stature. KCS2 is an autosomal leading hereditary condition.