Monilethrix: A rare hereditary condition
Monilethrix is a rare hereditary condition generally considered to be an autosomal-dominant disorder with variable penetrance. Here, we report a case of monilethrix in a 13-year-old boy with an affected sibling. A therapeutic trial with oral N-acetyl cysteine was attempted. There was slight improvem...
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Format: | Book |
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Wolters Kluwer Medknow Publications,
2013-01-01T00:00:00Z.
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A1234.567 |
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Copy 1 | Available |