• Thumbnail for Camurati–Engelmann disease
    CamuratiEngelmann disease (CED) is a very rare autosomal dominant genetic disorder that causes characteristic anomalies in the skeleton. It is also known...
    13 KB (1,625 words) - 04:16, 22 June 2024
  • Thumbnail for Hyperostosis
    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...
    2 KB (281 words) - 15:22, 15 March 2024
  • Silverman Calvé disease – Jacques Calvé CamuratiEngelmann disease (aka CamuratiEngelmann 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...
    850 bytes (127 words) - 07:58, 6 May 2023
  • Thumbnail for Osteopetrosis
    sclerosing skeletal dysplasias, progressive diaphyseal dysplasia (CamuratiEngelmann disease), SOST-related sclerosing skeletal dysplasias. Besides, the differential...
    26 KB (2,741 words) - 03:51, 3 May 2024
  • Thumbnail for Bone density
    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
  • Thumbnail for Osteosclerosis
    Mixed sclerosing bone dysplasia Progressive diaphyseal dysplasia (CamuratiEngelmann disease) SOST-related sclerosing bone dysplasias Sclerosis of the bones...
    8 KB (698 words) - 21:54, 7 June 2024
  • syndrome Camptodactyly vertebral fusion Campylobacteriosis CamuratiEngelmann disease Canavan leukodystrophy Candidiasis Chronic mucocutaneous candidiasis...
    40 KB (3,648 words) - 19:46, 6 May 2024
  • Thumbnail for Osteogenesis imperfecta
    /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 CamuratiEngelmann disease Proventricular dilatation disease, also known as "macaw wasting disease" Percentage depth dose curve...
    2 KB (254 words) - 18:01, 22 July 2023
  • Thumbnail for Ghosal hematodiaphyseal dysplasia
    synthase, which produces Thromboxane A2. Although this disease is like CamuratiEngelmann disease where there is also diaphyseal dysplasia, there are, however...
    15 KB (1,704 words) - 02:38, 24 July 2022
  • Thumbnail for TGF beta 1
    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
  • Thumbnail for Index of trauma and orthopaedics articles
    Bumper fracture - Bunion - Burst fracture Calcaneal fracture - CamuratiEngelmann disease - Cancellous bone - Cartilage - Cartilaginous joint - Catel–Manzke...
    17 KB (1,534 words) - 16:16, 20 July 2022
  • Thumbnail for Malignant infantile osteopetrosis
    Malignant infantile osteopetrosis (category Rare diseases)
    Mixed sclerosing bone dysplasia Progressive diaphyseal dysplasia (CamuratiEngelmann disease) SOST-related sclerosing bone dysplasias The only effective line...
    7 KB (699 words) - 18:16, 17 June 2023
  • Albers-Schonberg disease Albright's hereditary osteodystrophy Antley–Bixler syndrome Apert syndrome Beals syndrome Bechterew's Bruck syndrome CamuratiEngelmann disease...
    9 KB (735 words) - 17:42, 20 March 2022
  • List of OMIM disorder codes (category Genetic diseases and disorders)
    vara-pericarditis syndrome; 208250; PRG4 CamuratiEngelmann 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 CamuratiEngelmann 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