See arthrochalasis on Wiktionary
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{ "head_templates": [ { "args": { "1": "-" }, "expansion": "arthrochalasis (uncountable)", "name": "en-noun" } ], "lang": "English", "lang_code": "en", "pos": "noun", "related": [ { "word": "dermatochalasis" } ], "senses": [ { "categories": [ "English entries with incorrect language header", "English lemmas", "English nouns", "English terms with quotations", "English uncountable nouns", "Entries with translation boxes", "Pages with 1 entry", "Pages with entries", "Terms with Portuguese translations", "en:Teratology" ], "examples": [ { "ref": "1936 June 27, F Ronchese, “Dermatorrhexis with dermatochalasis and arthrochalasis (the so-called Ehlers-Danlos syndrome)”, in American Journal of Diseases of Children, volume 51, number 6, page 1403:", "text": "The so-called Danlos or Ehlers-Danlos syndrome consists of three symptoms: (1) pronounced fragility of the skin and its blood vessels, with breaking, splitting and the formation of hematomas and pseudotumors subsequent to the slightest trauma (dermatorrhexis-fragilitas cutis), (2) a more or less pronounced hyperlaxity and hyperelasticity of the skin (dermatochalasis-laxitas cutis) and (3) more or less pronounced hyperlaxity or hyperflexibility of the joints (arthrochalasis-laxitas articularis).", "type": "quote" }, { "ref": "1973 June 27, JR Owen, “Generalized hypermobility of joints: arthrochalasis multiplex congenita.”, in Archives of Disease in Childhood, volume 48, number 6, page 487:", "text": "Generalized hypermobility of joints has been reviewed by Hass and Hass (1958) who described 5 patients in detail and called the condition arthrochalasis multiplex congenita; they noted that little attention had been paid previously to the orthopaedic manifestations and stressed that generalized hypermobility could exist without skin laxity; they suggested that it was an entity separable from Ehlers-Danlos syndrome and that joint involvement was very variable.", "type": "quote" }, { "ref": "2014, Jaroslava Halper, Progress in Heritable Soft Connective Tissue Diseases, page 130:", "text": "The classic, hypermobility and vascular subtype of EDS are the most common, whereas the kyphoscoliosis, arthrochalasis and dermatosparaxis types constitute very rare conditions.", "type": "quote" } ], "glosses": [ "A rare form of Ehlers-Danlos syndrome, characterised by very loose joints and dislocations involving both hips." ], "links": [ [ "teratology", "teratology" ], [ "Ehlers-Danlos syndrome", "Ehlers-Danlos syndrome" ], [ "joint", "joint" ], [ "dislocation", "dislocation" ], [ "hip", "hip" ] ], "raw_glosses": [ "(teratology) A rare form of Ehlers-Danlos syndrome, characterised by very loose joints and dislocations involving both hips." ], "tags": [ "uncountable" ], "topics": [ "medicine", "sciences", "teratology" ] } ], "translations": [ { "code": "pt", "lang": "Portuguese", "sense": "disorder characterised by very loose joints", "tags": [ "feminine" ], "word": "artrocalasia" } ], "word": "arthrochalasis" }
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This page is a part of the kaikki.org machine-readable All languages combined dictionary. This dictionary is based on structured data extracted on 2024-11-28 from the enwiktionary dump dated 2024-11-21 using wiktextract (65a6e81 and 0dbea76). The data shown on this site has been post-processed and various details (e.g., extra categories) removed, some information disambiguated, and additional data merged from other sources. See the raw data download page for the unprocessed wiktextract data.
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