Monilethrix: a typical case report with microscopic and dermatoscopic findings
Monilethrix is a rare hereditary condition generally considered to be an autosomal dominant disorder with variable penetrance. A case of a 6-year-old girl without a familial background for this disease is reported. The diagnosis was made by optic microscopy and dermoscopy. A therapeutic trial with t...
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| Main Authors: | , |
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| Format: | Book |
| Published: |
Sociedade Brasileira de Dermatologia,
2015-02-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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| Summary: | Monilethrix is a rare hereditary condition generally considered to be an autosomal dominant disorder with variable penetrance. A case of a 6-year-old girl without a familial background for this disease is reported. The diagnosis was made by optic microscopy and dermoscopy. A therapeutic trial with topical minoxidil was conducted. |
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| Item Description: | 0365-0596 10.1590/abd1806-4841.20153357 |