"pseudohemophilia" meaning in English

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  "etymology_text": "From international scientific vocabulary, reflecting New Latin combining forms: pseudo- + hemophilia.",
  "forms": [
    {
      "form": "pseudohemophilias",
      "tags": [
        "plural"
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  "lang": "English",
  "lang_code": "en",
  "pos": "noun",
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        {
          "ref": "1959, Hermansky F, Pudlak P, “Albinism associated with hemorrhagic diathesis and unusual pigmented reticular cells in the bone marrow: report of two cases with histochemical studies”, in Blood, volume 14, number 2, →DOI, →PMID, pages 162–169",
          "text": "On examining hemostasis, the only consistent abnormal laboratory finding was a prolonged bleeding time, so that the hemorrhagic disorder fell into the group of so-called pseudohemophilias.",
          "type": "quotation"
        },
        {
          "ref": "2013, Gadisseur A, Berneman Z, Schroyens W, Michiels JJ, “Pseudohemophilia of Erik von Willebrand caused by homozygous one nucleotide deletion in exon 18 of the VW-factor gene”, in World J Hematol, volume 2, number 4, →DOI, pages 99–108",
          "text": "The original description of a novel severe bleeding disorder as \"Hereditary Pseudohemophilia\" by Erik von Willebrand can currently be labelled as von Willebrand disease (VWD) type 3. […] [¶] All five daughters, who died from uncontrolled bleedings, very likely would have been homozygous for the deletion in exon 18 consistent with pseudohemophilia, now called VWD type 3. […] [¶] These data demonstrate that the original family S, described by Erik von Willebrand as pseudohemophilia A, has to be diagnosed as autosomal recessive VWD type 3 caused by a homozygous null mutation (one nuclotide deletion of exon 18).",
          "type": "quotation"
        }
      ],
      "glosses": [
        "Any of several disorders of prolonged blood clotting time, seeming clinically similar to the hemophilias, but pathophysiologically different therefrom, without the same clotting factor derangements as found therein; at least some of these disorders are types of von Willebrand disease, and nowadays would be called and diagnosed thus."
      ],
      "hypernyms": [
        {
          "word": "von Willebrand disease"
        }
      ],
      "id": "en-pseudohemophilia-en-noun-9wAzuMRl",
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          "prolonged",
          "prolonged#Adjective"
        ],
        [
          "clotting",
          "clot#Verb"
        ],
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          "hemophilias",
          "hemophilia#Noun"
        ],
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          "pathophysiologically",
          "pathophysiology#Noun"
        ],
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          "von Willebrand disease",
          "von Willebrand disease#Noun"
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      "raw_glosses": [
        "(medicine, dated) Any of several disorders of prolonged blood clotting time, seeming clinically similar to the hemophilias, but pathophysiologically different therefrom, without the same clotting factor derangements as found therein; at least some of these disorders are types of von Willebrand disease, and nowadays would be called and diagnosed thus."
      ],
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        {
          "word": "hemopathology"
        },
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          "word": "hematology"
        }
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        "classical compound",
        "international scientific vocabulary"
      ]
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  ],
  "sounds": [
    {
      "other": "/ˌsudoʊˌhiːməˈfiːliə/"
    }
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  "word": "pseudohemophilia"
}

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  ],
  "etymology_text": "From international scientific vocabulary, reflecting New Latin combining forms: pseudo- + hemophilia.",
  "forms": [
    {
      "form": "pseudohemophilias",
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  "lang_code": "en",
  "pos": "noun",
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          "ref": "1959, Hermansky F, Pudlak P, “Albinism associated with hemorrhagic diathesis and unusual pigmented reticular cells in the bone marrow: report of two cases with histochemical studies”, in Blood, volume 14, number 2, →DOI, →PMID, pages 162–169",
          "text": "On examining hemostasis, the only consistent abnormal laboratory finding was a prolonged bleeding time, so that the hemorrhagic disorder fell into the group of so-called pseudohemophilias.",
          "type": "quotation"
        },
        {
          "ref": "2013, Gadisseur A, Berneman Z, Schroyens W, Michiels JJ, “Pseudohemophilia of Erik von Willebrand caused by homozygous one nucleotide deletion in exon 18 of the VW-factor gene”, in World J Hematol, volume 2, number 4, →DOI, pages 99–108",
          "text": "The original description of a novel severe bleeding disorder as \"Hereditary Pseudohemophilia\" by Erik von Willebrand can currently be labelled as von Willebrand disease (VWD) type 3. […] [¶] All five daughters, who died from uncontrolled bleedings, very likely would have been homozygous for the deletion in exon 18 consistent with pseudohemophilia, now called VWD type 3. […] [¶] These data demonstrate that the original family S, described by Erik von Willebrand as pseudohemophilia A, has to be diagnosed as autosomal recessive VWD type 3 caused by a homozygous null mutation (one nuclotide deletion of exon 18).",
          "type": "quotation"
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        "Any of several disorders of prolonged blood clotting time, seeming clinically similar to the hemophilias, but pathophysiologically different therefrom, without the same clotting factor derangements as found therein; at least some of these disorders are types of von Willebrand disease, and nowadays would be called and diagnosed thus."
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        ],
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          "hemophilias",
          "hemophilia#Noun"
        ],
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          "pathophysiologically",
          "pathophysiology#Noun"
        ],
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          "von Willebrand disease",
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      "raw_glosses": [
        "(medicine, dated) Any of several disorders of prolonged blood clotting time, seeming clinically similar to the hemophilias, but pathophysiologically different therefrom, without the same clotting factor derangements as found therein; at least some of these disorders are types of von Willebrand disease, and nowadays would be called and diagnosed thus."
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      "other": "/ˌsudoʊˌhiːməˈfiːliə/"
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  "word": "pseudohemophilia"
}