Copyright © Philip M. Parker, INSEAD. Terms of Use.
| Domain | Definition |
Health | A heterogeneous group of inherited collagen diseases. The most common manifestions of Ehlers-Danlos Syndrome are hyperextensible skin and joints, skin fragility and reduced wound healing capability. (references) |
Medicine | Hyperelastic and fragile skin, hyperflexible joints, and fragile blood vessels, with resulting hematomata which sometimes develops into pseudotumors. The condition has a hereditary tendency and often affects the skin of the eyelids. Source: European Union. (references) |
Source: compiled by the editor from various references; see credits. | |
(From Wikipedia, the free Encyclopedia)
Source: adapted by the editor from Wikipedia, the free encyclopedia under a copyleft GNU Free Documentation License (GFDL) from the article "Ehlers-Danlos syndrome."
| Domain | Title |
References | |
Books | |
Source: compiled by the editor from various references; see credits. | |
| Subject | Topic | Quote |
Health | Such disorders include Marfan Syndrome and Ehlers-Danlos Syndrome. (references) | |
Systemic diseases, such as Leber's congenital amaurosis, Ehlers-Danlos syndrome, Down syndrome, and osteogenesis imperfecta. (references) | ||
There are more than 200 HDCTs, among them Ehlers-Danlos syndrome, epidermolysis bullosa, Marfan syndrome, and osteogenesis imperfecta. (references) | ||
Source: compiled by the editor from ICON Group International, Inc.; see credits. | ||
| Language | Translations for "EHLERS-DANLOS SYNDROME"; alternative meanings/domain in parentheses. | ||||||||||
Danish | Ehlers-Danlos'syndrom (arthrochalasis-multiplex congenita, cutis elastica, cutis hyperelastica, elastic skin), cutis hyperelastica (arthrochalasis-multiplex congenita, cutis elastica, cutis hyperelastica, elastic skin). (various references) | ||||||||||
Dutch | Ehler-Danlos-syndroom (arthrochalasis-multiplex congenita, cutis hyperelastica), mesenchymose (arthrochalasis-multiplex congenita, cutis hyperelastica). (various references) | ||||||||||
Finnish | Ehlers-Danlosin oireyhtymä (arthrochalasis-multiplex congenita, cutis hyperelastica). (various references) | ||||||||||
French | syndrome d'Ehlers-Danlos, maladie d'Ehler-Danlos, dermatosparaxie. (various references) | ||||||||||
German | Ehlers-Danlos Syndrom (fibrodysplasia hyperelastica, Meekeren-Ehlers-Danlos synddrome), Ehlers-Danlos Krankheit (fibrodysplasia hyperelastica, Meekeren-Ehlers-Danlos synddrome), Mesenchymose (fibrodysplasia hyperelastica, Meekeren-Ehlers-Danlos synddrome), Meekeren-Ehlers-Danlos Syndrom (fibrodysplasia hyperelastica, Meekeren-Ehlers-Danlos synddrome), Fibrodysplasia elastica generalisata (fibrodysplasia hyperelastica, Meekeren-Ehlers-Danlos synddrome), Dystrophia mesodermalis congenita (fibrodysplasia hyperelastica, Meekeren-Ehlers-Danlos synddrome), Danlos Syndrom (fibrodysplasia hyperelastica, Meekeren-Ehlers-Danlos synddrome). (various references) | ||||||||||
Greek | νόσος Ehler-Danlos (arthrochalasis-multiplex congenita, cutis hyperelastica), δερματοσπαραξία (arthrochalasis-multiplex congenita, cutis hyperelastica). (various references) | ||||||||||
Italian | sindrome di Ehlers-Danlos (arthrochalasis-multiplex congenita, cutis elastica, cutis hyperelastica, elastic skin). (various references) | ||||||||||
Pig Latin | ehlers-danlosay yndromesay síndrome del hombre de goma (arthrochalasis-multiplex congenita, cutis hyperelastica), síndrome de Ehlers-Danlos (arthrochalasis-multiplex congenita, cutis hyperelastica, fibrodysplasia hyperelastica, Meekeren-Ehlers-Danlos synddrome), fibrodisplasis hiperelástica (arthrochalasis-multiplex congenita, cutis hyperelastica), fibrodisplasia elástica generalizada (arthrochalasis-multiplex congenita, cutis hyperelastica). (various references) | ||||||||||
| Language | Period | Translations |
| Latin | 500 BCE-Modern | cutis hyperelastica. (various references) |
| Source: compiled by the editor from various references. | ||
Hexadecimal (or equivalents, 770AD-1900s) (references)45 48 4C 45 52 53 2D 44 41 4E 4C 4F 53 53 59 4E 44 52 4F 4D 45 |
| Leonardo da Vinci (1452-1519; backwards) (references)
|
Binary Code (1918-1938, probably earlier) (references)01000101 01001000 01001100 01000101 01010010 01010011 00101101 01000100 01000001 01001110 01001100 01001111 01010011 00100000 01010011 01011001 01001110 01000100 01010010 01001111 01001101 01000101 |
HTML Code (1990) (references)E H L E R S - D A N L O S   S Y N D R O M E |
ISO 10646 (1991-1993) (references)0045 0048 004C 0045 0052 0053 002D 0044 0041 004E 004C 004F 0053 0053 0059 004E 0044 0052 004F 004D 0045 |
Encryption (beginner's substitution cypher): (references)3942463952531538354846495325359483852494739 |
| 1. Usage: Commercial 2. Quotations: Non-fiction 3. Translations: Modern 4. Translations: Ancient | 5. Orthography 6. Bibliography |
Copyright © Philip M. Parker, INSEAD. Terms of Use.
