Literature DB >> 2785251

Progressive intracranial calcification in dihydropteridine reductase deficiency prior to folinic acid therapy.

R C Woody1, M A Brewster, C Glasier.   

Abstract

Hyperphenylalaninemia in infants and children may be caused by a deficiency of dihydropteridine reductase (DHPR). Recommended therapy includes folinic acid as a source of tetrahydrofolate, a phenylalanine-restricted diet, and both dopamine and serotonin precursors. We report a child with progressive basal ganglia and other subcortical calcifications prior to the use of folinic acid. Six other reported cases of DHPR deficiency demonstrated similar calcifications prior to folinic acid therapy. Since this pattern of calcification also resembles that seen in CNS folate deficiency caused by both congenital folate deficiency and that which is methotrexate-induced, we propose that intracranial calcification in DHPR deficiency is caused by inadequate CNS tetrahydrofolate and may be prevented by the use of folinic acid. Our patient achieved excellent seizure control following the use of folinic acid, suggesting either a direct or indirect anticonvulsant effect of this compound in patients with DHPR deficiency.

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Year:  1989        PMID: 2785251     DOI: 10.1212/wnl.39.5.673

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  8 in total

1.  An international survey of patients with tetrahydrobiopterin deficiencies presenting with hyperphenylalaninaemia.

Authors:  Thomas Opladen; Georg F Hoffmann; Nenad Blau
Journal:  J Inherit Metab Dis       Date:  2012-06-23       Impact factor: 4.982

2.  Epilepsy and intracranial calcification of unknown origin.

Authors:  Ethem M Arsava; Serap Saygi
Journal:  J Neurol       Date:  2005-04-15       Impact factor: 4.849

3.  Recessive developmental delay, small stature, microcephaly and brain calcifications with locus on chromosome 2.

Authors:  Anna Rajab; Kimberly A Aldinger; Hisham Ali El-Shirbini; William B Dobyns; M Elizabeth Ross
Journal:  Am J Med Genet A       Date:  2009-02       Impact factor: 2.802

Review 4.  Disorders of biopterin metabolism.

Authors:  Nicola Longo
Journal:  J Inherit Metab Dis       Date:  2009-02-09       Impact factor: 4.982

5.  Tetrahydrobiopterin deficiencies: Lesson from clinical experience.

Authors:  Ayse Ergul Bozaci; Esra Er; Havva Yazici; Ebru Canda; Sema Kalkan Uçar; Merve Güvenc Saka; Cenk Eraslan; Hüseyin Onay; Sara Habif; Beat Thöny; Mahmut Coker
Journal:  JIMD Rep       Date:  2021-02-01

6.  Molecular docking simulations provide insights in the substrate binding sites and possible substrates of the ABCC6 transporter.

Authors:  Mohammad Jakir Hosen; Abdullah Zubaer; Simrika Thapa; Bijendra Khadka; Anne De Paepe; Olivier M Vanakker
Journal:  PLoS One       Date:  2014-07-25       Impact factor: 3.240

Review 7.  Consensus guideline for the diagnosis and treatment of tetrahydrobiopterin (BH4) deficiencies.

Authors:  Thomas Opladen; Eduardo López-Laso; Elisenda Cortès-Saladelafont; Toni S Pearson; H Serap Sivri; Yilmaz Yildiz; Birgit Assmann; Manju A Kurian; Vincenzo Leuzzi; Simon Heales; Simon Pope; Francesco Porta; Angeles García-Cazorla; Tomáš Honzík; Roser Pons; Luc Regal; Helly Goez; Rafael Artuch; Georg F Hoffmann; Gabriella Horvath; Beat Thöny; Sabine Scholl-Bürgi; Alberto Burlina; Marcel M Verbeek; Mario Mastrangelo; Jennifer Friedman; Tessa Wassenberg; Kathrin Jeltsch; Jan Kulhánek; Oya Kuseyri Hübschmann
Journal:  Orphanet J Rare Dis       Date:  2020-05-26       Impact factor: 4.123

8.  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
  8 in total

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