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lipochondrodystrophy

/ˌlɪp.əˌkɒn.drəʊˈdɪs.trə.fi/

Tradução: Doença hereditária autossômica recessiva causada por distúrbio do metabolismo dos mucopolissacarídeos, que provoca anomalias graves do desenvolvimento da cartilagem e dos ossos e deficiência intelectual.

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noun

/ˌlɪp.əˌkɒn.drəʊˈdɪs.trə.fi/C2formalmedical
  • ptDoença hereditária autossômica recessiva causada por distúrbio do metabolismo dos mucopolissacarídeos, que provoca anomalias graves do desenvolvimento da cartilagem e dos ossos e deficiência intelectual.

A hereditary autosomal recessive disorder involving a defect in mucopolysaccharide metabolism, leading to severe abnormalities in the development of skeletal cartilage and bone, as well as mental retardation.

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  1. Lipochondrodystrophyformalmedical

    An autosomal recessive hereditary disorder affecting mucopolysaccharide metabolism, leading to severe skeletal and cartilage deformities, bone abnormalities, and mental retardation.

    ptLipocondrodistrofia

    • The child was diagnosed with lipochondrodystrophy shortly after birth due to abnormal skeletal development.
    • Genetic counseling is recommended for families with a history of lipochondrodystrophy.
    • Treatment for lipochondrodystrophy focuses on managing symptoms and supportive care.

    Sinônimosgargoylism

Formas
  • lipochondrodystrophies plural form
  • lipochondrodystrophies' possessive plural form
  • lipochondrodystrophy's possessive singular form