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[Menkes' disease: anatomo-clinical presentation of a case]
M A Martínez-Granero1, D Hardisson, A Martínez-Bermejo
1Servicio de Neurologia Pediátrica, Hospital La Paz, Madrid, España.
Abstract:
We describe a case of Menke's disease with severe neurological involvement, convulsive crises and characteristic hair anomalies (scanty, fragile, macroscopically hypopigmented and microscopically kinked) which led to rapid diagnosis. Vascular abnormalities with elongated, twisted arteries, skeletal abnormalities (more wormian cranial bones than usual, lateral spurs of metaphyses) and vesicle diverticuli. Electron microscopy of skeletal muscle showed concentrically laminated bodies, possibly of mitochondrial origin. Respiratory chain enzyme activity was normal. The patient died at the age of two and a half. On necropsy, histological abnormalities characteristics of the illness were seen (loss of neurones in the granular layer of the cerebellum, the neurones of Purkinje had thickening of the dendrites which spread out in the form of a weeping willow, reduplication and fragmentation of the internal elastic layer of muscle arteries). In the cortex of the cerebellum mega-mitochondria with electron-dense bodies, were seen on electron microscopy. This is the first case of Menke's disease described in the Spanish literature which includes pathology and electron microscope studies.
Insights
Menke
Area of Science:
- Pediatric Neurology
- Medical Genetics
- Pathology
Background:
- Menke's disease is a rare genetic disorder affecting copper metabolism.
- It typically presents with neurological deterioration and characteristic hair abnormalities.