"arthrochalasis" meaning in All languages combined

{
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      "expansion": "arthrochalasis (uncountable)",
      "name": "en-noun"
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  "lang": "English",
  "lang_code": "en",
  "pos": "noun",
  "senses": [
    {
      "categories": [
        {
          "kind": "other",
          "name": "English entries with incorrect language header",
          "parents": [
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          "source": "w"
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          "langcode": "en",
          "name": "Teratology",
          "orig": "en:Teratology",
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      "examples": [
        {
          "ref": "1936 June 25, 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": "quotation"
        },
        {
          "ref": "1973 June 25, 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": "quotation"
        },
        {
          "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": "quotation"
        }
      ],
      "glosses": [
        "A rare form of Ehlers-Danlos syndrome, characterised by very loose joints and dislocations involving both hips."
      ],
      "id": "en-arthrochalasis-en-noun-2~VKmN3Z",
      "links": [
        [
          "teratology",
          "teratology"
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        [
          "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."
      ],
      "related": [
        {
          "word": "dermatochalasis"
        }
      ],
      "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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  "lang": "English",
  "lang_code": "en",
  "pos": "noun",
  "related": [
    {
      "word": "dermatochalasis"
    }
  ],
  "senses": [
    {
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        "English lemmas",
        "English nouns",
        "English terms with quotations",
        "English uncountable nouns",
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      "examples": [
        {
          "ref": "1936 June 25, 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": "quotation"
        },
        {
          "ref": "1973 June 25, 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": "quotation"
        },
        {
          "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": "quotation"
        }
      ],
      "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"
        ],
        [
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          "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"
      ],
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        "medicine",
        "sciences",
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  ],
  "translations": [
    {
      "code": "pt",
      "lang": "Portuguese",
      "sense": "disorder characterised by very loose joints",
      "tags": [
        "feminine"
      ],
      "word": "artrocalasia"
    }
  ],
  "word": "arthrochalasis"
}