محدث, غلامعلی and عاملی, حسین (2008) APLASIA CUTIS CONGENITAL (ACC). J Urmia Univ Med Sci., 19 (1). pp. 72-76.


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Aplasia Cutis Congenital (ACC) is the most common benign isolated defect but it can be associated with other physical anomalies or malformation and syndromes. No unifying theory can account for all lesions of ACC. Because this condition is the phenotypic result of more than one disease process it is likely that more than one mechanism is involved. Mechanisms include genetic factors, teratogens, compromised vasculature to the skin, and trauma. Frieden created a classification system for ACC consisting of 9 groups based on number and location of acc and the presence or absence of associated malformations1. Materials & Methods: In this observational cross-sectional study, a census method for gathering information was used. The obtained data were analyzed descriptively via EP16 software. we have studied 20 newborns, 9 males, and 11 females with skin defects, from September 1997 to September 2005 in Akbarabadi hospital. Results: In this study, the skin lesions of 85% were single, 65% on the scalp, 50% on the vertex, 5% on parietal, 15% on parietoocciputal, 15% on lumbosacral, 20% on extremities, and 15% with trisomy13. Mothers of two newborns had the history of drug use and abuse during pregnancy. Extensive skin lesions during neonatal period have high mortality rate, in our study also the rate of mortality with extensive lesions were 55%. Conclusion:�According to this study isolated skin defect was observed in most of the cases (85%), and the most signifant cause of newborns’ mortality with skin defect was sepsis.

Item Type: Article
Uncontrolled Keywords: Aplasia, Congenital, Cutaneous absence, Aplasia skin
Subjects: R Medicine > R Medicine (General)
Depositing User: Unnamed user with email gholipour.s@umsu.ac.ir
Date Deposited: 02 Jan 2018 06:44
Last Modified: 02 Jan 2018 06:44
URI: http://eprints.umsu.ac.ir/id/eprint/3698

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