Details

Autor(en) / Beteiligte

• GIRE, C
• GIRARD, N
• NICAISE, C
• EINAUDI, M. A
• MONTFORT, M. F
• DEJODE, J. M

Titel

Clinical features and neuroradiological findings of mitochondrial pathology in six neonates

Ist Teil von

• Child's nervous system, 2002-11, Vol.18 (11), p.621-628

Ort / Verlag

Berlin: Springer

Erscheinungsjahr

2002

Link zum Volltext

Quelle

SpringerLINK Contemporary (Konsortium Baden-Württemberg)

Beschreibungen/Notizen

• We hoped to itemize the clinical and neuroradiological features of six neonates with mitochondrial disorders. We examined a case series of six neonates. The diagnosis of mitochondrial cytopathy was made on the basis of spectrophotometric measurements of respiratory chain enzyme activities in skeletal muscle biopsy specimens. Magnetic resonance (MR) imaging was performed in all cases. The antenatal onset in five cases and the lack of any symptom-free interval are suggestive of fetal expression of the disease. No specific symptoms were found: arthrogryposis congenita multiplex in one, progressive hepatocellular dysfunction in three, encephalomyelopathy and cardiomyopathy in four. Complex I deficiency was found in three patients, while one patients had a defect of complex IV and the last a combined defect of complexes I and IV. Neuroradiological findings were either cerebral atrophy or white matter abnormalities of the brain stem in all cases but one and gave additional information, because clinical symptoms are not quite specific. The combination of clinical and MRI findings in neonatal cases can rule out hypoxic ischemic encephalopathy, which suggests an additional screening method to look for mitochondrial disorder.