2015
DOI: 10.1590/abd1806-4841.20153357
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Monilethrix: a typical case report with microscopic and dermatoscopic findings

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.

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Cited by 22 publications
(20 citation statements)
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“…Patient always felt several small nodules in the scalp, more over the occipital area. Family history confirmed that brother, sister, mother and family members from mother's side have the same problem with their hair though with varying severity [1].…”
Section: Case Reportmentioning
confidence: 86%
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“…Patient always felt several small nodules in the scalp, more over the occipital area. Family history confirmed that brother, sister, mother and family members from mother's side have the same problem with their hair though with varying severity [1].…”
Section: Case Reportmentioning
confidence: 86%
“…Body hair was thin, nails were deformed showed koilonychia. Patient had no other skin lesions, or anomalies [1]. General and systemic examination was normal.…”
Section: Clinical Examination and Trichoscopymentioning
confidence: 95%
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“…A comprehensive review of the epidemiology of HS 1 reported data ranging from <0.1% 2,3 to 8%, 4 allowing the Authors to conclude that the prevalence of HS may approach that of psoriasis. 1 Starting from this statement, we compared occurrence data of HS with those of psoriasis in a large clinical data set collected in a dermatological reference centre, to provide a 'ballpark' estimate of prevalence and incidence of HS in Italy.…”
mentioning
confidence: 99%