Camurati-Englemann Syndrome
Subject
Subject Source: Medical Subject Headings
Scope Note: Notes = An autosomal dominant form of dysplasia that is characterized by progressive thickening of diaphyseal cortex of long bones. Mutations in the gene that encodes TRANSFORMING GROWTH FACTOR BETA1 are one cause of this disorder.,Created For = LHSA-Dott
Found in 1 Collection or Record:
PR1.950, 1967-1979
Item
Identifier: LHB1 CC/20/PR1.950
Scope and Contents
Correspondence relating to male and female patients. Conditions mentioned include: intracranial pressure; Engelmann Camurati disorder; and osteosclerosis.
Dates:
1967-1979