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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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Bibliografski detalji
Glavni autori: Vikramkumar, Adaikalampillai Ganapathy, Kuruvila, Sheela, Ganguly, Satyaki
Format: Artigo
Jezik:Inglês
Izdano: Medknow Publications & Media Pvt Ltd 2013
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3667317/
https://ncbi.nlm.nih.gov/pubmed/23723505
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0019-5154.110869
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