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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Bibliographic Details
Main Authors: Adaikalampillai Ganapathy Vikramkumar (Author), Sheela Kuruvila (Author), Satyaki Ganguly (Author)
Format: Book
Published: Wolters Kluwer Medknow Publications, 2013-01-01T00:00:00Z.
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3rd Floor Main Library

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Call Number: A1234.567
Copy 1 Available