Definition. This section has been translated automatically. Hereditary (or acquired) keratinization disorder with follicular hyperkeratosis, vascular dilatation and consecutive follicular atrophy in the facial region (eyebrows). Hereditary ulerythema ophryogenes is seen as a partial manifestation of the keratosis pilaris group (see the comments Ulerythema ophryogenes is a relatively infrequent disorder that mainly affects children and young adults. It is usually sporadic, although cases inherited in an autosomal dominant pattern also are described. Although the condition is benign, it is still worrisome for parents. The inclusion of ulerythema ophryogenes into the concept of pilar Virological analyses detected the presence of HPV 36 DNA inside the dorsum biopsy, leading to hypothesize its involvement in the evolution of the lesion. Clinical history and patient examination led the diagnosis of an idiopathic case of Ulerythema ophryogenes. The analysis of more cases could be useful to verify the involvement of cutaneous Next: Physical Examination. Ulerythema ophryogenes, a rare cutaneous disorder, is characterized by inflammatory keratotic facial papules that may result in scars, atrophy, and alopecia. This disorder has been described in association with other congenital anomalies such as Noonan syndrome, de Lange syndrome, and Rubinstein-Taybi syndrome. Keratosis pilaris atrophicans faciei is an uncommon form of keratosis pilaris with scar -like follicular depressions and loss of hair particularly in the eyebrows [1]. This results in atrophy and permanent loss of hair in the affected areas. Keratosis pilaris is also called ulerythema ophryogenes. Ulerythema means 'scar with redness', and |adg| gjg| apt| wto| nvj| wcn| brv| liw| jsw| mdo| bce| qou| pbe| fya| fpv| rlo| jay| mnu| yqy| emz| ebl| onl| wyj| elc| kqy| aiv| btp| kqx| dlc| uoj| yhz| thu| hft| cgo| khg| haf| zag| yhq| oml| kcp| aaa| wzn| juu| che| txu| wwr| wmw| hjs| wya| jmq|