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1.931  Articles
1 of 194 pages  |  10  records  |  more records»
IntroductionAplasia cutis congenita is a rare disorder presenting with absence of portion of skin over localized or wide spread area. Aplasia cutis congenita affects approximately 1 in 10,000 newborns. The incidence of the nonsyndromic form is unknown. Th... see more

Adams-Oliver syndrome was first described in 1945 as a multiple congenital malformations association including aplasia cutis congenita and terminal transverse limb defects, along with cardiovascular and central nervous system anomalies. We report the case... see more

ABS 1. CALVARIAL AGENESIS AND APLASIA CUTIS CONGENITA: A CASE REPORT • F.P. Bunjamin, R.D. RoeslaniABS 2. NEUROCUTANEOUS MELANOSIS IN A NEWBORN • R. Tameliene, A. Vinskaite, J. Buinauskiene, R. DzikieneABS 3. TLR2/TLR6 HETERODIMER-MEDIATED INNATE IMMUNE R... see more

La aplasia cutis congénita es un trastorno raro y heterogéneo con una incidencia estimada de 1-3 casos por cada 10.000 nacimientos. Puede aparecer de manera aislada o formando parte de varios síndromes polimalformativos, observándose patrones de herencia ... see more

La aplasia cutis congénita es una patología que abarca un grupo heterogéneo de formas clínicas presentes desde el momento del nacimiento. Se caracteriza por la ausencia de todas las capas de la piel en algunas zonas del organismo y su presentación más fre... see more

BACKGROUND: Cutis marmorata telangiectatic congenital or Van Lohuizen syndrome is a rare vascular disorder that may be associated with other congenital malformations. Around 300 cases have been reported so far.CASE REPORT: We present a 4-year-old girl wit... see more

El Síndrome de Adams-Oliver (SAO) es una genodermatosis infrecuente, con casos esporádicos y familiares, de herencia autosómica dominante, aunque la herencia autosómica recesiva también se ha demostrado, con expresividad variable intra e interfamiliar, ca... see more



1 of 194 pages  |  10  records  |  more records»