Monilethrix: a typical case report with microscopic and dermatoscopic findings
An. bras. dermatol
;
90(1): 126-127, Jan-Feb/2015. graf
Article
in English
| LILACS
| ID: lil-735741
ABSTRACT
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.
Full text:
Available
Index:
LILACS (Americas)
Main subject:
Dermoscopy
/
Monilethrix
Type of study:
Diagnostic study
Limits:
Child
/
Female
/
Humans
Language:
English
Journal:
An. bras. dermatol
Journal subject:
Dermatology
Year:
2015
Type:
Article
Affiliation country:
Brazil
Institution/Affiliation country:
Fundação Oswaldo Cruz/BR
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