Charcot Marie Tooth Disease Type 1 - Rare but Commonest Hereditary Neuropathy
Objective: To present a case of Charcot Marie Tooth Disease. Backgrounds: A 22 years old boy presented with very slowly progressive symmetrical weakness of both lower limbs with distal muscular atrophy. He has a family member with similar problem. Methods: The patient was clinically examined and inv...
Tallennettuna:
| Päätekijät: | , |
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| Aineistotyyppi: | Kirja |
| Julkaistu: |
Al Ameen Medical College,
2012-01-01T00:00:00Z.
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| Aiheet: | |
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Internet
Connect to this object online.3rd Floor Main Library
| Hyllypaikka: |
A1234.567 |
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| Nide 1 | Saatavissa |