Vocab Bloom Hub

neurofibromatosis

/ˌnjʊə.rəʊ.faɪ.brəʊ.məˈtəʊ.sɪs/

Traducción: Enfermedad genética autosómica dominante caracterizada por el desarrollo de múltiples neurofibromas, manchas cutáneas y, frecuentemente, anomalías del desarrollo.

1 entrada

noun

/ˌnjʊə.rəʊ.faɪ.brəʊ.məˈtəʊ.sɪs/C2formalmedical
  • esEnfermedad genética autosómica dominante caracterizada por el desarrollo de múltiples neurofibromas, manchas cutáneas y, frecuentemente, anomalías del desarrollo.

An autosomal dominant genetic disorder characterized by the development of multiple neurofibromas, skin spots, and often associated with developmental abnormalities.

incontable

  1. Genetic disorderC2formalmedical

    An autosomal dominant genetic condition characterized by the growth of noncancerous tumors (neurofibromas) along nerves, skin spots (café-au-lait spots), and sometimes developmental abnormalities.

    esNeurofibromatosis

    • Neurofibromatosis is often diagnosed in childhood due to the appearance of café-au-lait spots.
    • Patients with neurofibromatosis may develop multiple neurofibromas on their skin.
    • Genetic testing can confirm a diagnosis of neurofibromatosis.
Formas
  • neurofibromatoses plural form
  • neurofibromatoses' possessive plural form
  • neurofibromatosis's possessive singular form