Literature DB >> 24927077

A new case of maternal phenylketonuria treated with sapropterin dihydrochloride (6R-BH4).

Luis Aldámiz-Echevarría1, Maria L Couce, Marta Llarena, Fernando Andrade.   

Abstract

PURPOSE: A woman with phenylketonuria (PKU) was diagnosed through neonatal screening, her PAH mutation was p.V388M/p.I65T, for which she received treatment with phenylalanine restriction, and was administered oral sapropterin dihydrochloride (6R-BH(4)) from the age of thirty. The purpose of this article is to describe the treatment with BH4 during her pregnancy and to evaluate a plan for its use.
METHODS: The patient had an unplanned pregnancy at 34 years of age, for which she received a phenylalanine-free supplement enriched with essential fatty acids, vitamins and trace elements.
RESULTS: The dose of 6R-BH(4) was reduced from 500 mg/day to 100 mg/day until its suspension in the 28th week of gestation, and was well tolerated. Blood phenylalanine control was easily accomplished during this pregnancy, and no nutritional deficiency was seen.
CONCLUSION: The pregnancy had a normal outcome, and so we consider that adaptation of the dose of 6R-BH(4) to the prenatal periods aided a greater efficiency and a lower risk in the treatment of maternal PKU.

Entities:  

Keywords:  Maternal phenylketonuria; phenylketonuria; sapropterin dihydrochloride; tetrahydrobiopterin

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Year:  2014        PMID: 24927077     DOI: 10.3109/09513590.2014.928688

Source DB:  PubMed          Journal:  Gynecol Endocrinol        ISSN: 0951-3590            Impact factor:   2.260


  1 in total

1.  The first study of successful pregnancies in Chinese patients with Phenylketonuria.

Authors:  Lin Wang; Fang Ye; Hui Zou; Kundi Wang; Zhihua Chen; Qin Hui; Bingjuan Han; Chun He; Xiaowen Li; Ming Shen
Journal:  BMC Pregnancy Childbirth       Date:  2020-04-28       Impact factor: 3.007

  1 in total

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