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Relato de Casos
Maternal phenylketonuria: a case report
- Ernesto Antonio Figueiró-Filho,
- Alessandro Henrique Antunes Lopes,
- Flávio Renato de Almeida Senefonte,
- Virgilio Gonçalves de Souza Júnior,
- Carlos Augusto Botelho, [ ... ],
- Geraldo Duarte
02-16-2004
Summary
Relato de CasosMaternal phenylketonuria: a case report
Revista Brasileira de Ginecologia e Obstetrícia. 2004;26(10):813-817
02-16-2004DOI 10.1590/S0100-72032004001000009
- Ernesto Antonio Figueiró-Filho,
- Alessandro Henrique Antunes Lopes,
- Flávio Renato de Almeida Senefonte,
- Virgilio Gonçalves de Souza Júnior,
- Carlos Augusto Botelho,
- Geraldo Duarte
Views84See moreMaternal phenylketonuria is an aminoacid pathology characterized by elevated plasma levels of phenylalanine in the pregnant woman that may cause abnormalities in fetus development, and which is called maternal phenylketonuria syndrome. As the clinical manifestations are non-specific, the disease should be diagnosed by laboratory screening. We present a case of a second pregnancy in a woman with a history of psycho-cognitive development retardation without previous obstetric history, with diagnosis of phenylketonuria in the present gestation, treated with specific phenylalanine-free diet. The newborn did not present congenital defects. The previous gestation without maternal treatment resulted in a child with serious developmental disturbances, microcephalia and auditory-speaking deficits. Early diagnosis and treatment of hyperphenylalaninemia during pregnancy are essential, mainly because of the negative impact on fetal development. In the here reported case, there were fetal benefits from the maternal dietary treatment, which demonstrates the importance of the maternal diagnosis of phenylketonuria in women in reproductive age.
Views84This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Summary
Relato de CasosMaternal phenylketonuria: a case report
Revista Brasileira de Ginecologia e Obstetrícia. 2004;26(10):813-817
02-16-2004DOI 10.1590/S0100-72032004001000009
- Ernesto Antonio Figueiró-Filho,
- Alessandro Henrique Antunes Lopes,
- Flávio Renato de Almeida Senefonte,
- Virgilio Gonçalves de Souza Júnior,
- Carlos Augusto Botelho,
- Geraldo Duarte
Views84See moreMaternal phenylketonuria is an aminoacid pathology characterized by elevated plasma levels of phenylalanine in the pregnant woman that may cause abnormalities in fetus development, and which is called maternal phenylketonuria syndrome. As the clinical manifestations are non-specific, the disease should be diagnosed by laboratory screening. We present a case of a second pregnancy in a woman with a history of psycho-cognitive development retardation without previous obstetric history, with diagnosis of phenylketonuria in the present gestation, treated with specific phenylalanine-free diet. The newborn did not present congenital defects. The previous gestation without maternal treatment resulted in a child with serious developmental disturbances, microcephalia and auditory-speaking deficits. Early diagnosis and treatment of hyperphenylalaninemia during pregnancy are essential, mainly because of the negative impact on fetal development. In the here reported case, there were fetal benefits from the maternal dietary treatment, which demonstrates the importance of the maternal diagnosis of phenylketonuria in women in reproductive age.
This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
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