Search on: PKU, MATERNAL 
Descriptors Found: 1
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Descriptor English:   Phenylketonuria, Maternal 
Descriptor Spanish:   Fenilcetonuria Materna 
Descriptor Portuguese:   Fenilcetonúria Materna 
Synonyms English:   Maternal Phenylalanine Hydroxylase Deficiency Disease
Maternal Phenylketonuria
PKU, Maternal
Phenylalanine Hydroxylase Deficiency Disease, Maternal
Phenylalanine-Hydroxylase Deficiency Disease, Maternal
Phenylketonuria, Pregnancy in
Pregnancy in Phenylketonuria  
Tree Number:   C10.228.140.163.100.687.500
C13.703.575
C16.320.565.100.766.500
C16.320.565.189.687.500
C18.452.132.100.687.500
C18.452.648.100.766.500
C18.452.648.189.687.500
Definition English:   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) 
Indexing Annotation English:   check the tags PREGNANCY & FEMALE; consider also PHENYLALANINE HYDROXYLASE /defic
See Related English:   Phenylalanine Hydroxylase
 
History Note English:   1992 
Allowable Qualifiers English:  
BL blood CF cerebrospinal fluid
CI chemically induced CL classification
DI diagnosis DG diagnostic imaging
DH diet therapy DT drug therapy
EC economics EN enzymology
EP epidemiology EH ethnology
ET etiology GE genetics
HI history IM immunology
ME metabolism MI microbiology
MO mortality NU nursing
PS parasitology PA pathology
PP physiopathology PC prevention & control
PX psychology RT radiotherapy
RH rehabilitation SU surgery
TH therapy UR urine
VE veterinary VI virology
Record Number:   29896 
Unique Identifier:   D017042 

Occurrence in VHL:
 

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DeCS