onychomadesis


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onychomadesis

 [on″ĭ-ko-mah-de´sis]
periodic separation of the proximal portions of the nail plate from the matrix and bed with subsequent shedding of the nails.

on·y·cho·ma·de·sis

(on'i-kō-mă-dē'sis),
Complete shedding of the nails, usually associated with systemic disease.
[onycho- + G. madēsis, a growing bald, fr. madaō, to be moist, (of hair) fall off]

onychomadesis

/on·y·cho·ma·de·sis/ (on″ĭ-ko-mah-de´sis) complete loss of the nails.

on·y·cho·ma·de·sis

(on'i-kō-mă-dē'sis)
Complete shedding of the nails, usually associated with systemic disease.
[onycho- + G. madēsis, a growing bald, fr. madaō, to be moist, (of hair) fall off]

onychomadesis

; onychoptosis; aplastic anonychia separation of the nail plate from the proximal nail bed ± transient arrest of nail growth and Beau's line formation; occurs secondary to local trauma (e.g. subungual haematoma), dermatopathologies characterized by matrix scarring, local inflammation or infection, peripheral vascular disease, severe Raynaud's, or as a familial trait

onychomadesis

complete loss of the nails (claws).
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References in periodicals archive ?
Fecal samples were obtained from children in clusters of cases or from children with sporadic onychomadesis cases and from their asymptomatic classmates or contacts who were exposed to onychomadesis patients.
Sixty-five fecal samples, collected from 44 onychomadesis case-patients (28 with HFMD) and 21 children who were exposed to onychomadesis case-patients (3 with HFMD), were tested for EVs.
A cluster of onychomadesis cases during May-July 2008 was first reported in childcare center 1 from which 17 samples from onychomadesis patients and exposed children were studied.
Sporadic onychomadesis cases that matched exclusion criteria for likely incidental infections were analyzed and presented HEV-B serotypes CVB3 (n = 2), E3 (n = 1), E9 (n = 2), and E3/E9 co-infection (n = 1).
Nine serotype CVB1 sequences were obtained from 6 onychomadesis case-patients (5 with previous HFMD) and 3 healthy classmates.
Serotype CVA10 was detected in 18 children: 12 onychomadesis case-patients (10 with HFMD) and 6 healthy children.
CVA6 serotype was found in 6 children: 3 from the onychomadesis outbreak reported in fall 2008 (childcare center 9) and 3 from patients with sporadic onychomadesis cases reported in summer 2008.
Three CVA5 isolates were detected in different children with onychomadesis after HFMD.
6% nt identity, were detected in samples from patients with sporadic onychomadesis cases, with and without previous HFMD.
One CVA16 isolate was detected in a child with sporadic HFMD followed by onychomadesis (isolate 54682); the child was not attending any childcare center.
The main EVs detected in the HFMD-onychomadesis outbreak in Valencia in 2008 included HEV-A serotypes that caused HFMD (CVA6 and CVA10) and an HEV-B serotype (CVB1), currently associated with meningitis and myocarditis and detected recently in clusters of severe systemic neonatal illness (25) and onychomadesis outbreaks (14,15).
For instance, the time from onset of HFMD and onychomadesis symptoms to specimen collection for isolate 54678 (90 and 47 days, respectively) and from onychomadesis onset to specimen collection in isolate 54720 (61 days), although both contained EV71 serotype, was considerably longer than the average from symptom onset to fecal sample collection (44 and 25 days for HFMD and onychomadesis, respectively).