Seizures and paroxysmal events: symptoms pointing to the diagnosis of pyridoxine-dependent epilepsy and pyridoxine phosphate oxidase deficiency.

Abstract

AIM:

We report on seizures, paroxysmal events, and electroencephalogram (EEG) findings in four female infants with pyridoxine-dependent epilepsy (PDE) and in one female with pyridoxine phosphate oxidase deficiency (PNPO).

METHOD:

Videos and EEGs were analysed and compared with videos of seizures and paroxysmal events archived from 140 neonates. PDE and PNPO were proven by complete control of seizures once pyridoxine or pyridoxal 5'-phosphate was administered and by recurrence when withdrawn. Mutations in the antiquitin gene were found in three patients and in the PNPO gene in one child.

RESULTS:

Seizures began within 48 hours after birth in four newborns and at age 3 weeks in one. Frequent multifocal and generalized myoclonic jerks, often intermixed with tonic symptoms, abnormal eye movement, grimacing, or irritability, were observed in all infants with PDE and PNPO, but rarely in the other archived videos of neonates. EEGs were inconstant and frequently no discernable ictal changes were recorded during the seizures and the paroxysmal events. In addition, interictal EEGs were inconclusive, with normal and abnormal recordings. In older children tonic-clonic seizures, abnormal behaviour, inconsolable crying, frightened facial expression, sleep disturbance, loss of consciousness, paraesthesia, or intermittent visual symptoms were described during controlled and uncontrolled withdrawal or insufficient dosage.

INTERPRETATION:

PDE or PNPO should be considered in infants with prolonged episodes of mixed multifocal myoclonic tonic symptoms, notably when associated with grimacing and abnormal eye movements.

• Authors: Bernhard Schmitt, Matthias Baumgartner, Philippa B Mills, Peter T Clayton, Cornelis Jakobs, Elmar Keller, Gabriele Wohlrab
• Journal: Developmental medicine and child neurology (Dev Med Child Neurol) Vol. 52 Issue 7 Pg. e133-42 (Jul 2010) ISSN: 1469-8749 [Electronic] England
• PMID: 20370816 (Publication Type: Case Reports, Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Anticonvulsants
• Pyridoxal Phosphate
• ALDH7A1 protein, human
• Aldehyde Dehydrogenase
• Pyridoxaminephosphate Oxidase
• Pyridoxine

Topics

• Aldehyde Dehydrogenase (genetics)
• Anticonvulsants (therapeutic use)
• Brain (physiopathology)
• Brain Diseases, Metabolic (diagnosis, drug therapy, physiopathology)
• Diagnosis, Differential
• Electroencephalography
• Epilepsy (diagnosis, drug therapy, physiopathology)
• Eye Movements
• Female
• Humans
• Infant, Newborn
• Mutation
• Pyridoxal Phosphate (therapeutic use)
• Pyridoxaminephosphate Oxidase (deficiency, genetics)
• Pyridoxine (therapeutic use)
• Retrospective Studies
• Seizures (diagnosis, drug therapy, physiopathology)
• Treatment Outcome
• Video Recording