Neuropediatrics 2002; 33(6): 301-308
DOI: 10.1055/s-2002-37082
Original Article

Georg Thieme Verlag Stuttgart · New York

Psychomotor Retardation, Spastic Paraplegia, Cerebellar Ataxia and Dyskinesia Associated with Low 5-Methyltetrahydrofolate in Cerebrospinal Fluid: A Novel Neurometabolic Condition Responding to Folinic Acid Substitution

V. T. Ramaekers 1 , M. Häusler 1 , T. Opladen 1 , G. Heimann 1 , N. Blau 2
  • 1Division of Paediatric Neurology, Department of Paediatrics, University Hospital Aachen, Aachen, Germany
  • 2Division of Clinical Chemistry and Biochemistry, University Children's Hospital, Zurich, Switzerland
Further Information

Publication History

Received: 10 April 2002

Accepted after Revision: 25 September 2002

Publication Date:
06 February 2003 (online)

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Abstract

Introduction

Normal brain development and function depend on the active transport of folates across the blood-brain barrier. The folate receptor-1 (FR 1) protein is localized at the basolateral surface of the choroid plexus, which is characterized by a high binding affinity for circulating 5-methyltetrahydrofolate (5-MTHF).

Patients and Methods

We report on the clinical and metabolic findings among five children with normal neurodevelopmental progress during the first four to six months followed by the acquisition of a neurological condition which includes marked irritability, decelerating head growth, psychomotor retardation, cerebellar ataxia, dyskinesias (choreoathetosis, ballism), pyramidal signs in the lower limbs and occasional seizures. After the age of six years the two oldest patients also manifested a central visual disorder. Known disorders have been ruled out by extensive investigations. Cerebrospinal fluid (CSF) analysis included determination of biogenic monoamines, pterins and 5-MTHF.

Results

Despite normal folate levels in serum and red blood cells with normal homocysteine, analysis of CSF revealed a decline towards very low values for 5-methyltetrahydrofolate (5-MTHF), which suggested disturbed transport of folates across the blood-brain barrier. Genetic analysis of the FR 1 gene revealed normal coding sequences. Oral treatment with doses of the stable compound folinic acid (0.5 - 1 mg/kg/day Leucovorin®) resulted in clinical amelioration and normalization of 5-MTHF values in CSF.

Conclusion

Our findings identified a new condition manifesting after the age of 6 months which was accompanied by low 5-MTHF in cerebrospinal fluid and responded to oral supplements with folinic acid. However, the cause of disturbed folate transfer across the blood-brain barrier remains unknown.

References

PD, M. D., Ph. D. V. T. Ramaekers

Division of Paediatric Neurology, Department of Paediatrics, University Hospital Aachen

Pauwelsstraße 30

52074 Aachen

Germany

Email: vramaekers@ukaachen.de