Kenny Caffey Syndrome

It is feasible that the primary title of the record Kenny-Caffey Syndrome is not the name you anticipated. Happy examine the words specifying to encounter the alternating name(s) as well as condition class(s) covered by this record.


  • dwarfism, cortical thickening of tubular bones & short-term hypocalcemia
  • KCS2
  • Kenny-Caffey disorder, leading kind

Condition Subdivisions

  • None

General Discussion
Kenny-Caffey disorder kind 2 (KCS2) is a very unusual genetic skeletal condition identified by thickening of the lengthy bones, slim marrow tooth cavities in the bones (medullary constriction), as well as problems impacting the head as well as eyes. The main end result of KCS2 is brief stature. KCS2 is an autosomal leading hereditary condition.

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