Volume 22, Issue 3 (Fall 1998)                   Research in Medicine 1998, 22(3): 60-65 | Back to browse issues page

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Shamsaldini S. Adams Oliver Syndrome and Congenital Deafness. Research in Medicine. 1998; 22 (3) :60-65
URL: http://pejouhesh.sbmu.ac.ir/article-1-2243-en.html
Kerman University of Medical Sciences, Kerman, Iran.
Abstract:   (1127 Views)
Admas-Oliver syndrome is a rare autosomal dominant disease of congenital development defects association with aplasia cutis. All of 81 reported cases were of 32 group families. These two cases had congenital scalp cutis aplasia with developmental defect and hypoplasia of left foot digits in case 1.Congenital deaf-mute in both can added to the past known findings in this syndrome. Thoracic deformity is a rare associated finding, but onychophagia with out any sign of affection in their parents are specific findings in these two cases.
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Type of Study: Original | Subject: Interdisciplinary (Educational Management, Educational research, Statistics, Medical education
Received: 2020/02/18 | Accepted: 2020/02/18 | Published: 2020/02/18

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