2006
DOI: 10.1111/j.1468-3083.2006.01564.x
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Pseudomonilethrix type II and pili bifurcati

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Cited by 10 publications
(10 citation statements)
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“…597,598 The defect may involve one of three keratin genes KRTHB6, KRTHB1, and KRTHB3. 604 The latter form may be the result of the compression of normal or fragile hairs between glass slides, prior to their microscopic examination. 601,602 Nail defects appear common with KRTHB1 defects.…”
Section: Monilethrixmentioning
confidence: 99%
“…597,598 The defect may involve one of three keratin genes KRTHB6, KRTHB1, and KRTHB3. 604 The latter form may be the result of the compression of normal or fragile hairs between glass slides, prior to their microscopic examination. 601,602 Nail defects appear common with KRTHB1 defects.…”
Section: Monilethrixmentioning
confidence: 99%
“…Pili bifurcati (PB) is a rare autosomal dominant hair shaft dysplasia that presents with thin, short, fragile hair on the scalp, eyelashes, and eyebrows . The condition is caused by bifurcation of the hair fiber at multiple irregular intervals; each bifurcation produces two separate parallel branches that fuse again to form a single shaft, and each successive branch's own cuticle completely surrounds it .…”
Section: Hair Shaft Disorders Without Fragilitymentioning
confidence: 99%
“…Scanning microscopy shows grooves and partial twisting of the hair, irregular cuticle, deep grooves splitting hairs into two segments, and optically empty cavities within cortical and medullary layers on cross section . Associations include mosaic trisomy 8 syndrome , cognitive defect , juvenile cataracts , dental abnormalities , ulcerative colitis , and pseudomonilethrix type II .…”
Section: Hair Shaft Disorders Without Fragilitymentioning
confidence: 99%
“…All patients showed a negative response to an autologous serum skin test (ASST). The ASST was performed according to the method described by Sabroe et al 9 Patients were examined twice: first, during the symptomatic period, and next, during complete spontaneous remission lasting for at least 4 months (range 4-6 months) without any medication.…”
Section: Department Of Dermatologymentioning
confidence: 99%
“…Pseudomonilethrix should be ruled out before establishing the diagnosis of monilethrix. Some authors suggest that pseudomonilethrix is an autosomal dominant inherited nodal trichodystrophy with late onset, 9 while others suggest iatrogenic pseudomonilethrix as a condition produced by the procedure of preparing hairs for microscopic examination which occurs when hairs are pressed together between glass slides. It appears as irregularly constricted hair shafts, depending on the pressure applied or on the presence of cosmetic haircare products at the visualized site under dermoscopy.…”
mentioning
confidence: 99%