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Adams-Oliver Syndrome - A Case Report.

作者信息

Srihari Sahana, Asha G S

机构信息

Department of Dermatology, Bangalore Medical College and Research Institute, Bengaluru, Karnataka, India.

出版信息

Indian Dermatol Online J. 2022 Dec 14;14(3):422-423. doi: 10.4103/idoj.idoj_330_22. eCollection 2023 May-Jun.

DOI:10.4103/idoj.idoj_330_22

PMID:37266096

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10231716/

Abstract

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fbf/10231716/e5d88afc62d0/IDOJ-14-422-g001.jpg

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引用本文的文献

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本文引用的文献

The spectra of clinical phenotypes in aplasia cutis congenita and terminal transverse limb defects.

Am J Med Genet A. 2009 Aug;149A(8):1860-81. doi: 10.1002/ajmg.a.32708.

Adams-Oliver syndrome: a case with complete expression.

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Clinical and molecular analysis of nine families with Adams-Oliver syndrome.

Eur J Hum Genet. 2003 Jun;11(6):457-63. doi: 10.1038/sj.ejhg.5200980.

Congenital scalp defects with distal limb anomalies (Adams-Oliver syndrome): report of ten cases and review of the literature.

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J Dermatol Case Rep. 2012 Mar 27;6(1):25-8. doi: 10.3315/jdcr.2012.1092.

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Ultrasound Obstet Gynecol. 2002 Nov;20(5):506-10. doi: 10.1046/j.1469-0705.2002.00839.x.

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Pediatr Rep. 2016 Jun 27;8(2):6517. doi: 10.4081/pr.2016.6517. eCollection 2016 Jun 15.

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Am J Med Genet A. 2013 Jun;161A(6):1386-9. doi: 10.1002/ajmg.a.35864. Epub 2013 Apr 23.

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Oxf Med Case Reports. 2025 Sep 28;2025(9):omaf176. doi: 10.1093/omcr/omaf176. eCollection 2025 Sep.

本文引用的文献

The spectra of clinical phenotypes in aplasia cutis congenita and terminal transverse limb defects.

Am J Med Genet A. 2009 Aug;149A(8):1860-81. doi: 10.1002/ajmg.a.32708.

Adams-Oliver syndrome: a case with complete expression.

J Dermatol. 2006 Jun;33(6):435-6. doi: 10.1111/j.1346-8138.2006.00104.x.

Clinical and molecular analysis of nine families with Adams-Oliver syndrome.

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Congenital scalp defects with distal limb anomalies (Adams-Oliver syndrome): report of ten cases and review of the literature.

Am J Med Genet. 1988 Sep;31(1):99-115. doi: 10.1002/ajmg.1320310112.