Literature DB >> 3987728

Congenital folate malabsorption.

L Corbeel, G Van den Berghe, J Jaeken, J Van Tornout, R Eeckels.   

Abstract

A Turkish girl presented with a history of fever, diarrhoea, convulsions, recurrent infections and failure to thrive from the age of 5 months. Megaloblastic anaemia was present and profound folate deficiency was evidenced in plasma and in CSF. Treatment with oral folic acid cured the anaemia, diarrhoea and infections but failed to prevent convulsions and the appearance of mental retardation and cerebral calcifications. Loading tests with folic acid and its derivatives led to the conclusion that the folate deficiency was caused by a defect in folate transport both across the gut and the blood-brain barrier. Low plasma concentrations of methionine prompted a therapeutic trial with methionine associated with vitamin B12 and folic acid that spectacularly improved the convulsions.

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Year:  1985        PMID: 3987728     DOI: 10.1007/bf00442302

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN: 0340-6199            Impact factor:   3.183


  25 in total

Review 1.  Folate binding proteins.

Authors:  S Waxman
Journal:  Br J Haematol       Date:  1975-01       Impact factor: 6.998

2.  Folate transport by the choroid plexus in vitro.

Authors:  R Spector; A V Lorenzo
Journal:  Science       Date:  1975-02-14       Impact factor: 47.728

3.  Letter: Congenital folate deficiency.

Authors:  P C Su
Journal:  N Engl J Med       Date:  1976-05-13       Impact factor: 91.245

4.  Congenital isolated defect of folic acid absorption.

Authors:  P J Santiago-Borrero; R Santini; E Pérez-Santiago; N Maldonado
Journal:  J Pediatr       Date:  1973-03       Impact factor: 4.406

5.  Transsulfuration in mammals. Microassays and tissue distributions of three enzymes of the pathway.

Authors:  S H Mudd; J D Finkelstein; F Irreverre; L Laster
Journal:  J Biol Chem       Date:  1965-11       Impact factor: 5.157

6.  Congenital malabsorption of folate.

Authors:  P Lanzkowsky
Journal:  Am J Med       Date:  1970-05       Impact factor: 4.965

7.  Pathogenesis of subacute combined degeneration: a result of methyl group deficiency.

Authors:  J M Scott; J J Dinn; P Wilson; D G Weir
Journal:  Lancet       Date:  1981-08-15       Impact factor: 79.321

8.  Congenital folate malabsorption.

Authors:  M Poncz; N Colman; V Herbert; E Schwartz; A Cohen
Journal:  J Pediatr       Date:  1981-11       Impact factor: 4.406

9.  Intracranial calcifications in childhood leukemia. An association with systemic chemotherapy.

Authors:  S McIntosh; D B Fischer; S G Rothman; N Rosenfield; J S Lobel; R O'Brien
Journal:  J Pediatr       Date:  1977-12       Impact factor: 4.406

10.  Transport of 5-methyltetrahydrofolic acid in erythrocytes from various mammalian species.

Authors:  R F Branda
Journal:  J Nutr       Date:  1981-04       Impact factor: 4.798

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  13 in total

1.  Biotin-responsive basal ganglia disease: a case diagnosed by whole exome sequencing.

Authors:  Kensaku Kohrogi; Eri Imagawa; Yuichiro Muto; Katsuki Hirai; Masahiro Migita; Hiroshi Mitsubuchi; Noriko Miyake; Naomichi Matsumoto; Kimitoshi Nakamura; Fumio Endo
Journal:  J Hum Genet       Date:  2015-04-16       Impact factor: 3.172

2.  CSF 5-Methyltetrahydrofolate Serial Monitoring to Guide Treatment of Congenital Folate Malabsorption Due to Proton-Coupled Folate Transporter (PCFT) Deficiency.

Authors:  A Torres; S A Newton; B Crompton; A Borzutzky; E J Neufeld; L Notarangelo; G T Berry
Journal:  JIMD Rep       Date:  2015-05-26

3.  Elevation of total homocysteine in the serum of patients with cobalamin or folate deficiency detected by capillary gas chromatography-mass spectrometry.

Authors:  S P Stabler; P D Marcell; E R Podell; R H Allen; D G Savage; J Lindenbaum
Journal:  J Clin Invest       Date:  1988-02       Impact factor: 14.808

Review 4.  The proton-coupled folate transporter (PCFT-SLC46A1) and the syndrome of systemic and cerebral folate deficiency of infancy: Hereditary folate malabsorption.

Authors:  Rongbao Zhao; Srinivas Aluri; I David Goldman
Journal:  Mol Aspects Med       Date:  2016-09-21

5.  Neurodevelopmental delay and focal seizures as presenting symptoms of human immunodeficiency virus I infection.

Authors:  P Habibi; S Strobel; I Smith; K Hyland; D W Howells; H Holzel; E M Brett; J Wilson; G Morgan; R J Levinsky
Journal:  Eur J Pediatr       Date:  1989-01       Impact factor: 3.183

6.  Congenital isolated folic acid malabsorption.

Authors:  J Urbach; A Abrahamov; N Grossowicz
Journal:  Arch Dis Child       Date:  1987-01       Impact factor: 3.791

Review 7.  Pteridines and mono-amines: relevance to neurological damage.

Authors:  I Smith; D W Howells; K Hyland
Journal:  Postgrad Med J       Date:  1986-02       Impact factor: 2.401

Review 8.  Inborn errors of metabolism underlying primary immunodeficiencies.

Authors:  Nima Parvaneh; Pierre Quartier; Parastoo Rostami; Jean-Laurent Casanova; Pascale de Lonlay
Journal:  J Clin Immunol       Date:  2014-08-01       Impact factor: 8.317

9.  A novel deletion mutation in the proton-coupled folate transporter (PCFT; SLC46A1) in a Nicaraguan child with hereditary folate malabsorption.

Authors:  N Diop-Bove; M Jain; F Scaglia; I D Goldman
Journal:  Gene       Date:  2013-06-28       Impact factor: 3.688

10.  The spectrum of mutations in the PCFT gene, coding for an intestinal folate transporter, that are the basis for hereditary folate malabsorption.

Authors:  Rongbao Zhao; Sang Hee Min; Andong Qiu; Antoinette Sakaris; Gary L Goldberg; Claudio Sandoval; J Jeffrey Malatack; David S Rosenblatt; I David Goldman
Journal:  Blood       Date:  2007-04-19       Impact factor: 22.113

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