| Autor: |
Kocen, R. S., King, R. H. M., Thomas, P. K., Haas, L. F. |
| Zdroj: |
Acta Neuropathologica; December 1973, Vol. 26 Issue: 4 p317-327, 11p |
| Abstrakt: |
Nerve biopsy findings are recorded for two previously reported patients with Tangier disease (hereditary high density lipoprotein deficiency). Both cases showed unusual clinical manifestations in comparison with other reported cases. The neurological disorder, symptoms from which began in the third decade, gave rise to a lower motor neuron deficit of unique distribution, which was accompanied by progressive sensory impairment limited for many years to loss of pain and temperature sensibility, ultimately involving all sensory modalities. |
| Databáze: |
Supplemental Index |
| Externí odkaz: |
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