What does camurati-engelmann syndrome mean?
Definitions for camurati-engelmann syndrome
ca·mu·rati-en·gel·man·n syn·drome
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Wikipedia
camurati-engelmann syndrome
Camurati–Engelmann disease (CED) is a very rare autosomal dominant genetic disorder that causes characteristic anomalies in the skeleton. It is also known as progressive diaphyseal dysplasia. It is a form of dysplasia. Patients typically have heavily thickened bones, especially along the shafts of the long bones (called diaphyseal dysplasia). The skull bones may be thickened so that the passages through the skull that carry nerves and blood vessels become narrowed, possibly leading to sensory deficits, blindness, or deafness. This disease often appears in childhood and is considered to be inherited, however many patients have no previous history of CED within their family. The disease is slowly progressive and, while there is no cure, there is treatment. It is named for M. Camurati and G. Engelmann.
U.S. National Library of Medicine
Camurati-Engelmann Syndrome
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.
Numerology
Chaldean Numerology
The numerical value of camurati-engelmann syndrome in Chaldean Numerology is: 8
Pythagorean Numerology
The numerical value of camurati-engelmann syndrome in Pythagorean Numerology is: 5
Translations for camurati-engelmann syndrome
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- Camurati-Engelmann syndroomDutch
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"camurati-engelmann syndrome." Definitions.net. STANDS4 LLC, 2024. Web. 1 May 2024. <https://www.definitions.net/definition/camurati-engelmann+syndrome>.
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