Number of the records: 1  

fenylketonúria matky

  1. Subject h.fenylketonúria matky
    Subject h.Phenylketonuria, Maternal
    Entry termschoroba z nedostatku fenylalanínhydroxylázy, v materstve
    tehotenstvo pri fenylketonúrii
    gravidita pri fenylketonúrii
    fenylketonúria maternálna
    English X referencesMaternal Phenylalanine Hydroxylase Deficiency Disease
    Pregnancy in Phenylketonuria
    Scope note in EnglishA condition occurring in untreated or partially treated females with PHENYLKETONURIA when they become pregnant. This may result in damages to the FETUS, including MICROCEPHALY; MENTAL RETARDATION; congenital heart disease; FETAL GROWTH RETARDATION; and CRANIOFACIAL ABNORMALITIES. (From Am J Med Genet 1997 Mar 3;69(1):89-95)
    See also reference (FX) in Slovak fenylalanínhydroxyláza
    See also reference (FX) in English Phenylalanine Hydroxylase
    Links (13) - ARTICLES
    (1) - MeSH descriptor
    (2) - BOOKS
    subject heading

    subject heading

Number of the records: 1  

  This site uses cookies to make them easier to browse. Learn more about how we use cookies.

Accept allSettingsReject all