It is feasible that the major title of the record Kenny-Caffey Syndrome is not the name you got. Kindly examine the words noting to discover the alternating name(s) and also condition neighborhood(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 exceptionally uncommon genetic skeletal problem identified by thickening of the lengthy bones, slim marrow dental caries in the bones (medullary constriction), as well as irregularities impacting the head and also eyes. The main result of KCS2 is brief stature. KCS2 is an autosomal leading hereditary condition.