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fenylketonúria matky
Record number d017042 Date 06.06.2025 Type M - MESH Topical term fenylketonúria matky Other term English (Pseudonym) Maternal Phenylalanine Hydroxylase Deficiency Disease
English (Pseudonym) Pregnancy in Phenylketonuria
Slovak (Pseudonym) choroba z nedostatku fenylalanínhydroxylázy, v materstve
Slovak (Pseudonym) tehotenstvo pri fenylketonúrii
Slovak (Pseudonym) gravidita pri fenylketonúrii
Slovak (Pseudonym) fenylketonúria maternálna
See also (Later heading) fenylalanínhydroxyláza
(Skutočné meno) fenylalanínhydroxyláza
UDC C10.228.140.163.100.687.500C12.050.703.575C16.320.565.100.766.500C16.320.565.189.687.500C18.452.132.100.687.500C18.452.648.100.766.500C18.452.648.189.687.500 Note A 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) subject heading
Number of the records: 1