Literature DB >> 28801146

BH4 deficiency identified in a neonatal screening program for hyperphenylalaninemia.

Cezar Antonio Abreu de Souza1, Michelle Rosa Andrade Alves2, Rosangelis Del Lama Soares2, Viviane de Cássia Kanufre3, Valéria de Melo Rodrigues4, Rocksane de Carvalho Norton4, Ana Lúcia Pimenta Starling4, Marcos José Burle de Aguiar4.   

Abstract

OBJECTIVES: To show the general prevalence and to characterize tetrahydrobiopterin (BH4) deficiencies with hyperphenylalaninemia, identified by the Neonatal Screening Program of the State of Minas Gerais.
METHODS: Descriptive study of patients with BH4 deficiency identified by the Neonatal Screening Program of the State of Minas Gerais.
RESULTS: The prevalence found was 2.1 for 1,000,000 live births, with a frequency of 1.71% among hyperphenylalaninemias. There were four cases (40%) with 6-pyruvoyl-tetrahydropterin synthase deficiency, three with GTP cyclohydrolase I - autosomal recessive form deficiency, and three with dihydropteridine reductase deficiency (30% each). Six patients were diagnosed due to clinical suspicion and four cases due to systematic screening in neonatal screening. After the start of the treatment, patients identified by neonatal screening had rapid improvement and improved neuropsychomotor development compared to those diagnosed by the medical history.
CONCLUSIONS: The prevalence of BH4 deficiencies in Minas Gerais was slightly higher than that found in the literature, but the frequency among hyperphenylalaninemias was similar. Although rare, they are severe diseases and, if left untreated, lead to developmental delays, abnormal movements, seizures, and premature death. Early treatment onset (starting before 5 months of age) showed good results in preventing intellectual disability, justifying the screening of these deficiencies in newborns with hyperphenylalaninemia identified at the neonatal screening programs for phenylketonuria.
Copyright © 2017 Sociedade Brasileira de Pediatria. Published by Elsevier Editora Ltda. All rights reserved.

Entities:  

Keywords:  Deficiência intelectual; Doenças raras; Fenilcetonúria; Intellectual disability; Neonatal screening; Phenylketonuria; Rare diseases; Triagem neonatal

Mesh:

Substances:

Year:  2017        PMID: 28801146     DOI: 10.1016/j.jped.2017.04.005

Source DB:  PubMed          Journal:  J Pediatr (Rio J)        ISSN: 0021-7557            Impact factor:   2.197


  4 in total

1.  Epidemiology of rare diseases in Brazil: protocol of the Brazilian Rare Diseases Network (RARAS-BRDN).

Authors:  Têmis Maria Félix; Bibiana Mello de Oliveira; Milena Artifon; Isabelle Carvalho; Filipe Andrade Bernardi; Ida V D Schwartz; Jonas A Saute; Victor E F Ferraz; Angelina X Acosta; Ney Boa Sorte; Domingos Alves
Journal:  Orphanet J Rare Dis       Date:  2022-02-24       Impact factor: 4.123

2.  Neonatal screening and genotype-phenotype correlation of hyperphenylalaninemia in the Chinese population.

Authors:  Xin Wang; Yanyun Wang; Dingyuan Ma; Zhilei Zhang; Yahong Li; Peiying Yang; Yun Sun; Tao Jiang
Journal:  Orphanet J Rare Dis       Date:  2021-05-12       Impact factor: 4.123

3.  Global prevalence of classic phenylketonuria based on Neonatal Screening Program Data: systematic review and meta-analysis.

Authors:  Hamid Reza Shoraka; Ali Akbar Haghdoost; Mohammad Reza Baneshi; Zohre Bagherinezhad; Farzaneh Zolala
Journal:  Clin Exp Pediatr       Date:  2020-02-06

4.  Dihydropyridine Reductase Deficiency: Acute Encephalopathy Related to Folinic Acid Treatment Interruption in a Girl.

Authors:  Maria Grazia Pappalardo; Alessandra Di Nora; Andrea Giugno; Concetta Meli; Annamaria Sapuppo; Piero Pavone; Agata Fiumara
Journal:  Glob Med Genet       Date:  2022-09-19
  4 in total

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