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Late diagnosis of phenylketonuria in a Bedouin mother.
- Source :
-
American journal of medical genetics [Am J Med Genet] 1992 Dec 01; Vol. 44 (6), pp. 713-5. - Publication Year :
- 1992
-
Abstract
- We report on the first case of phenylketonuria in a Bedouin woman with 3 children having the phenylketonuria embryofetopathy. Herein, we discuss briefly hazards of late diagnosis of maternal phenylketonuria.
- Subjects :
- Abortion, Habitual etiology
Adult
Child, Preschool
Female
Heart Defects, Congenital embryology
Heart Defects, Congenital etiology
Humans
Infant
Intellectual Disability embryology
Intellectual Disability etiology
Male
Maternal-Fetal Exchange
Microcephaly embryology
Microcephaly etiology
Phenylalanine administration & dosage
Phenylalanine metabolism
Phenylketonurias diet therapy
Phenylketonurias genetics
Pregnancy
Pregnancy Complications
Tyrosine blood
Fetal Diseases etiology
Phenylketonurias diagnosis
Subjects
Details
- Language :
- English
- ISSN :
- 0148-7299
- Volume :
- 44
- Issue :
- 6
- Database :
- MEDLINE
- Journal :
- American journal of medical genetics
- Publication Type :
- Academic Journal
- Accession number :
- 1481837
- Full Text :
- https://doi.org/10.1002/ajmg.1320440603