Table 3

Details of children referred to PIND with a suggested diagnosis of Alpers’ syndrome

CaseExpert Group decisionAge at presentationDeath reportedSeizuresTypical EEGTypical VEPLiver dysfunctionLiver biopsyMuscle biopsyBrain biopsy
Typical EEGs and VEPs are described in table 3. “Mitochondrial” in respect of liver and muscle biopsies refers to the conclusion given by the pathologist reviewing the material. Salient details of the pathology are given in the results section.
EEG, electroencephalogram; ND, not done; VEP, visual evoked potentials; ? not recorded.
1Alpers’ syndrome19 monthsYesGeneralisedNo?YesAlpers’“mitochondrial”Alpers’
2Alpers’ syndrome8 monthsYesMyoclonicNoYesYesAlpers’NormalND
3Mitochondrial encephalomyopathy3¼ yearsYesMyoclonicNoNDNo“mitochondrial”“mitochondrial”ND
4Mitochondrial encephalomyopathy1 yearNoMyoclonicNoYesYesNDNDND
5Mitochondrial encephalomyopathy9 monthsYesGeneralisedNoNoYes“mitochondrial”NormalND
6HIV encephalopathy6 monthsNoSpasmsNo?YesNDNDND
7Neuronal ceroid lipofuscinosis6½ yearsYesGeneralisedNoNoYesNDNDNot Alpers’
8Undiagnosed neurodegenerative disorder1½ yearsNoGeneralisedNoNoYesNDNDND
9Undiagnosed neurodegenerative disorder1 yearYesGeneralisedNoNoNoNormalNormalND
10Undiagnosed neurodegenerative disorder2 yearsNoGeneralised“Alpersish”NoYesFatty change onlyNDND
11Undiagnosed neurodegenerative disorder4 monthsNoGeneralisedNo?NoNDNDND