Volume 32, Issue S1 pp. 273-278
Short Report

Secondary disorders of glycosylation in inborn errors of fructose metabolism

E. Quintana

E. Quintana

Institut de Bioquímica Clínica, Servei de Bioquímica i Genètica Molecular, Hospital Clínic, Edificio Helios III, c/Mejia Lequerica s/n, Barcelona, 08028 Spain

CIBER de Enfermedades Raras (CIBERER), Barcelona, Spain

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L. Sturiale

L. Sturiale

CNR—Istituto per la Chimica e la Tecnologia dei Polimeri ICTP, Catania, Italy

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R. Montero

R. Montero

Servei de Bioquímica, Hospital Sant Joan de Déu, Barcelona, Spain

CIBER de Enfermedades Raras (CIBERER), Barcelona, Spain

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F. Andrade

F. Andrade

Servicio de Pediatría, Hospital de Cruces, Bilbao, Spain

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C. Fernandez

C. Fernandez

Institut de Bioquímica Clínica, Servei de Bioquímica i Genètica Molecular, Hospital Clínic, Edificio Helios III, c/Mejia Lequerica s/n, Barcelona, 08028 Spain

CIBER de Enfermedades Raras (CIBERER), Barcelona, Spain

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M. L. Couce

M. L. Couce

Servicio de Pediatría, Hospital Universitario de Santiago, Santiago de Compostela, Spain

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R. Barone

R. Barone

CNR—Istituto per la Chimica e la Tecnologia dei Polimeri ICTP, Catania, Italy

Center for Inherited Metabolic Diseases, Department of Pediatrics, University of Catania, Catania, Italy

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L. Aldamiz-Echevarria

L. Aldamiz-Echevarria

Servicio de Pediatría, Hospital de Cruces, Bilbao, Spain

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A. Ribes

A. Ribes

Institut de Bioquímica Clínica, Servei de Bioquímica i Genètica Molecular, Hospital Clínic, Edificio Helios III, c/Mejia Lequerica s/n, Barcelona, 08028 Spain

CIBER de Enfermedades Raras (CIBERER), Barcelona, Spain

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R. Artuch

R. Artuch

Servei de Bioquímica, Hospital Sant Joan de Déu, Barcelona, Spain

CIBER de Enfermedades Raras (CIBERER), Barcelona, Spain

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P. Briones

Corresponding Author

P. Briones

Institut de Bioquímica Clínica, Servei de Bioquímica i Genètica Molecular, Hospital Clínic, Edificio Helios III, c/Mejia Lequerica s/n, Barcelona, 08028 Spain

Consejo Superior de Investigaciones Científicas, Barcelona, Spain

CIBER de Enfermedades Raras (CIBERER), Barcelona, Spain

[email protected]

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First published: 20 September 2009
Citations: 32

Communicating editor: Jaak Jaeken

Competing interests: None declared

References to electronic databases: Hereditary fructose intolerance: OMIM 229600. Fructose-1,6-bisphosphatase deficiency: OMIM 229700. Aldolase B: EC 4.1.2.13. Fructose-1,6-bisphosphatase: EC 3.1.3.11.

Summary

Adamowicz and colleagues raised the alert in 2007 about patients with atypical hereditary fructose intolerance (HFI) primarily misdiagnosed as CDG Ix. We describe a girl with neonatal hypertonia, facial trismus, absent swallowing and coughing reflexes, gastro-oesophageal reflux and sporadically elevated Krebs cycle metabolites and lactate. At 14 months microcephaly and hepatomegaly were noted, with hypertransaminasaemia but normal blood coagulation, glucose, phosphate, and absent urinary reducing substances. Neurological impairment persisted. Because of hepatic and neurological abnormalities with developmental delay, Tf IEF was performed and showed a severe type 1 pattern, resulting in a wrong diagnosis of CDG. Subsequently, an aversion to fruits suggested HFI, confirmed by the finding of ALDOB mutations (p.A150P/p.N335K). The girl improved with fructose-free diet, but liver cirrhosis led to hepatic transplantation. She is now 7 years old with good evolution; facial trismus and hypertonia reversed, but microcephaly persists. Transferrin MALDI-TOF MS characterization revealed underoccupation of glycosylation sites and glycan abnormalities, which reversed with dietary treatment. High maternal fructose concentrations might have caused neonatal abnormalities. Although in our patient's mother there is no fructose accumulation at present, it is possible that increased ingestion of fruits and vegetables during pregnancy, together with her heterozygosity, caused an accumulation of fructose that finally affected the fetus. We also describe slightly abnormal transferrin isoelectric focusing and MALDI-TOF MS patterns of intact transferrin and N-glycans in a fructose-1,6-bisphosphatase (FBP1)-deficient patient. While HFI is a well-known cause of secondary CDG, we found no reports of abnormal transferrin isoelectric focusing patterns in FBP1 deficiency and we introduce this condition as a possible secondary cause for altered transferrin isoelectric focusing.

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