Literature DB >> 20548894

A case of adams-oliver syndrome.

Jong-Keun Seo1, Ju-Hyun Kang, Hyun-Jae Lee, Deborah Lee, Ho-Suk Sung, Seon-Wook Hwang.   

Abstract

Adams-Oliver syndrome (AOS) is a congenital condition characterized by aplasia cutis congenita, transverse limb defects, and cutis marmorata telangiectatica. AOS can also be associated with extensive lethal anomalies of internal organs, including the central nervous, cardiopulmonary, gastrourointestinal, and genitourinary systems. Generally, the more severe these interrelated anomalies are, the poorer the prognosis becomes. In the relevant literature on this topic, it is somewhat unclear as to whether the prognosis of AOS without lethal anomalies alters the lifespan. We report a case of AOS with typical skin defects only, and no internal organ anomalies.

Entities:  

Keywords:  Adams-Oliver syndrome; Aplasia cutis congenita; Cutis marmorata telangiectatica

Year:  2010        PMID: 20548894      PMCID: PMC2883411          DOI: 10.5021/ad.2010.22.1.96

Source DB:  PubMed          Journal:  Ann Dermatol        ISSN: 1013-9087            Impact factor:   1.444


  8 in total

1.  Adams-Oliver syndrome: a case with complete expression.

Authors:  Naveen Sankhyan; Ram Krishan Kaushal; Ranbir Singh Jaswal
Journal:  J Dermatol       Date:  2006-06       Impact factor: 4.005

2.  Adams-Oliver syndrome with widespread CMTC and fatal pulmonary vascular disease.

Authors:  Ophelia Entsir Dadzie; Lidia Tyszczuk; Susan E Holder; Fernanda Teixeira; Aikaterina Charakida; Julia Scarisbrick; Anthony Chu
Journal:  Pediatr Dermatol       Date:  2007 Nov-Dec       Impact factor: 1.588

Review 3.  The wide spectrum of clinical expression in Adams-Oliver syndrome: a report of two cases.

Authors:  M Mempel; D Abeck; I Lange; K Strom; A Caliebe; A Beham; M Kautza; W I Worret; B A Neubauer; J Ring; H Schröder; R Fölster-Holst
Journal:  Br J Dermatol       Date:  1999-06       Impact factor: 9.302

4.  Autosomal recessive type of Adams-Oliver syndrome: prenatal diagnosis.

Authors:  R Becker; J Kunze; D Horn; A Gasiorek-Wiens; M Entezami; R Rossi; M Guschmann; N Sarioglu
Journal:  Ultrasound Obstet Gynecol       Date:  2002-11       Impact factor: 7.299

5.  Adams-Oliver syndrome: clinical description of a four-generation family and exclusion of five candidate genes.

Authors:  P Verdyck; B Blaumeiser; M Holder-Espinasse; W Van Hul; W Wuyts
Journal:  Clin Genet       Date:  2006-01       Impact factor: 4.438

Review 6.  Adams-Oliver syndrome in siblings with central nervous system findings, epilepsy, and developmental delay: refining the features of a severe autosomal recessive variant.

Authors:  Robin R McGoey; Yves Lacassie
Journal:  Am J Med Genet A       Date:  2008-02-15       Impact factor: 2.802

7.  Adams-Oliver syndrome: a sporadic occurrence with minimal disease expression.

Authors:  Tarun Narang; Amrinder Jit Kanwar; Sunil Dogra
Journal:  Pediatr Dermatol       Date:  2008 Jan-Feb       Impact factor: 1.588

Review 8.  An autopsy case of Adams-Oliver syndrome.

Authors:  S Y Jun; S K Khang; S H Park
Journal:  J Korean Med Sci       Date:  2000-08       Impact factor: 2.153

  8 in total
  5 in total

Review 1.  A practical approach to the evaluation and treatment of an infant with aplasia cutis congenita.

Authors:  S R Humphrey; X Hu; K Adamson; A Schaus; J N Jensen; B Drolet
Journal:  J Perinatol       Date:  2017-10-19       Impact factor: 2.521

2.  Adams-Oliver Syndrome. A case with isolated aplasia cutis congenita and skeletal defects.

Authors:  Ola Bakry; Abdalla Attia; Eman Nabil El Shafey
Journal:  J Dermatol Case Rep       Date:  2012-03-27

3.  Adams-Oliver Syndrome: A Case with Full Expression.

Authors:  Amir Dehdashtian; Masoud Dehdashtian
Journal:  Pediatr Rep       Date:  2016-06-27

4.  Adams-Oliver Syndrome: A Rare Congenital Disorder.

Authors:  Sumara Rashid; Saleha Azeem; Samiha Riaz
Journal:  Cureus       Date:  2022-03-18

5.  A Case of Adams-Oliver Syndrome.

Authors:  Minoo Saeidi; Fahime Ehsanipoor
Journal:  Adv Biomed Res       Date:  2017-12-28
  5 in total

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