Kenny-Caffey syndrome

(ken'ē kaf'ē), a disorder characterized by intermittent hypocalcemia (associated with abnormalities in parathyroid hormone secretion) and bone and eye abnormalities; autosomal dominant and autosomal recessive forms exist, caused by mutation in the gene encoding tubulin-specific chaperone E on 1q.

Ken·ny-Caf·fey syn·drome

(ken'ē-kaf'ē sin'drōm) A disorder characterized by intermittent hypocalcemia (associated with abnormalities in parathyroid hormone secretion) and bone and eye abnormalities; autosomal dominant and autosomal recessive forms exist.

单词	kenny-caffey syndrome
释义	Kenny-Caffey syndrome Kenny-Caffey syndrome (ken'ē kaf'ē), a disorder characterized by intermittent hypocalcemia (associated with abnormalities in parathyroid hormone secretion) and bone and eye abnormalities; autosomal dominant and autosomal recessive forms exist, caused by mutation in the gene encoding tubulin-specific chaperone E on 1q. Ken·ny-Caf·fey syn·drome (ken'ē-kaf'ē sin'drōm) A disorder characterized by intermittent hypocalcemia (associated with abnormalities in parathyroid hormone secretion) and bone and eye abnormalities; autosomal dominant and autosomal recessive forms exist. AcronymsSeeKCS
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