Catalog

Kenny-Caffey syndrome, autosomal recessive

No MMS code

Link to WHO Definition

Kenny-Caffey syndrome, autosomal recessive – http://id.who.int/icd/entity/740581484

Sanjad-Sakati syndrome is characterised by congenital hypoparathyroidism, growth retardation, intellectual deficit, seizures, and dysmorphic features including microcephaly, facial, ocular and dental abnormalities, and short hands and feet.