Camurati–Engelmann disease (CED) is a very rare autosomal dominant genetic disorder that causes characteristic anomalies in the skeleton. It is also known...
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musculoskeletal disorders. Disorders featuring hyperostosis include: Camurati-Engelmann disease, type 2 Hypertrophic osteoarthropathy, primary, autosomal recessive...
3 KB (199 words) - 15:04, 30 November 2023
electrotherapy stimulation, therapeutic brain stimulation Camurati-Engelmann disease, also called "Camurati Engelmann syndrome" (CES) Carboxylesterase, an enzyme that...
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Silverman Calvé disease – Jacques Calvé Camurati–Engelmann disease (aka Camurati–Engelmann syndrome) – M. Camurati, G. Engelmann Canavan disease – Myrtelle...
62 KB (6,514 words) - 09:17, 9 July 2024
CED may refer to: CED (journal) Canadian Eskimo Dog Camurati-Engelmann disease, a rare genetic syndrome Capacitance Electronic Disc, a playback-only video...
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Osteopetrosis (redirect from Marble bone disease)
sclerosing skeletal dysplasias, progressive diaphyseal dysplasia (Camurati–Engelmann disease), SOST-related sclerosing skeletal dysplasias. Besides, the differential...
26 KB (2,741 words) - 03:51, 3 May 2024
several rare genetic diseases that have been associated with pathologic changes in bone mineral density. The table summarizes these diseases: Bone+Density at...
18 KB (1,936 words) - 19:45, 3 July 2024
Mixed sclerosing bone dysplasia Progressive diaphyseal dysplasia (Camurati–Engelmann disease) SOST-related sclerosing bone dysplasias Sclerosis of the bones...
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syndrome Camptodactyly vertebral fusion Campylobacteriosis Camurati–Engelmann disease Canavan leukodystrophy Candidiasis Chronic mucocutaneous candidiasis...
40 KB (3,648 words) - 19:46, 6 May 2024
Osteogenesis imperfecta (redirect from Brittle bone disease)
/ˌɒstioʊˈdʒɛnəsɪs ˌɪmpɜːrˈfɛktə/; OI), colloquially known as brittle bone disease, is a group of genetic disorders that all result in bones that break easily...
150 KB (15,363 words) - 14:58, 14 July 2024
dysplasia, also known as Camurati–Engelmann disease Proventricular dilatation disease, also known as "macaw wasting disease" Percentage depth dose curve...
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synthase, which produces Thromboxane A2. Although this disease is like Camurati–Engelmann disease where there is also diaphyseal dysplasia, there are, however...
15 KB (1,704 words) - 02:38, 24 July 2022
Niikawa N, Tomita Ha (January 2000). "Genetic mapping of the Camurati-Engelmann disease locus to chromosome 19q13.1-q13.3". Am. J. Hum. Genet. 66 (1):...
19 KB (2,290 words) - 20:43, 26 March 2024
Bumper fracture - Bunion - Burst fracture Calcaneal fracture - Camurati–Engelmann disease - Cancellous bone - Cartilage - Cartilaginous joint - Catel–Manzke...
17 KB (1,534 words) - 16:16, 20 July 2022
Malignant infantile osteopetrosis (category Rare diseases)
Mixed sclerosing bone dysplasia Progressive diaphyseal dysplasia (Camurati–Engelmann disease) SOST-related sclerosing bone dysplasias The only effective line...
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Albers-Schonberg disease Albright's hereditary osteodystrophy Antley–Bixler syndrome Apert syndrome Beals syndrome Bechterew's Bruck syndrome Camurati–Engelmann disease...
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List of OMIM disorder codes (category Genetic diseases and disorders)
vara-pericarditis syndrome; 208250; PRG4 Camurati–Engelmann disease; 131300; TGFB1 Canavan disease; 271900; ASPA Candidiasis, familial chronic mucocutaneous...
234 KB (18,877 words) - 15:43, 9 May 2024
wheelchair himself. His wheelchair use was a result of a bone disease called Camurati–Engelmann disease. The Rules of Charity, like most of Belluso's work, explores...
16 KB (2,354 words) - 22:34, 10 April 2024
he began using a wheelchair at the age of 13 due to a bone disease, Camurati-Engelmann syndrome. He completed both Bachelors and Masters degrees at...
3 KB (360 words) - 04:25, 4 April 2022