Phenylketonuria, Maternal [fenylketonurie v těhotenství]
topical
18
- Terms
-
mateřská fenylketonurie
mateřská PKU
těhotenství při fenylketonurii
-
Maternal Phenylalanine Hydroxylase Deficiency Disease
Maternal Phenylketonuria
Phenylalanine-Hydroxylase Deficiency Disease, Maternal
PKU, Maternal
Pregnancy in Phenylketonuria
Persistent link
https://www.medvik.cz/link/D017042
Definition
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)
- Annotation
- check the tags PREGNANCY & FEMALE; consider also PHENYLALANINE HYDROXYLASE /defic
- DUI
- D017042 MeSH Browser
- CUI
- M0025897
- Previous indexing
- Phenylketonuria (1966-1991)
- History note
- 1992
- Public note
- 1992
Allowable subheadings
- BL
- blood 0
- CF
- cerebrospinal fluid 0
- CI
- chemically induced 0
- CL
- classification 0
- DI
- diagnosis 4
- DG
- diagnostic imaging 0
- DH
- diet therapy 6
- DT
- drug therapy 0
- EC
- economics 0
- EN
- enzymology 0
- EP
- epidemiology 0
- EH
- ethnology 0
- ET
- etiology 1
- GE
- genetics 2
- HI
- history 0
- IM
- immunology 0
- ME
- metabolism 1
- MI
- microbiology 0
- MO
- mortality 0
- NU
- nursing 0
- PS
- parasitology 0
- PA
- pathology 0
- PP
- physiopathology 0
- PC
- prevention & control 1
- PX
- psychology 0
- RT
- radiotherapy 0
- RH
- rehabilitation 0
- SU
- surgery 0
- TH
- therapy 0
- UR
- urine 0
- VE
- veterinary 0
- VI
- virology 0
...
Occurrences in Medvik records
C
Diseases