Literature DB >> 19881996

Bart's syndrome.

Aruna Rajpal1, R Mishra, K Hajirnis, M Shah, N Nagpur.   

Abstract

A new-born girl presented with congenital absence of skin on the right leg and nail abnormalities. On second day of life, she developed multiple blistering skin lesions and died on seventeenth day of life. A positive family history of two other siblings, one male and one female who had blistering skin lesions and died within one and a half month of birth, was present. The diagnosis of Bart's syndrome was made on clinical presentation, family history and skin biopsy.

Entities:  

Keywords:  Bart's syndrome; congenital absence of skin

Year:  2008        PMID: 19881996      PMCID: PMC2763726          DOI: 10.4103/0019-5154.41655

Source DB:  PubMed          Journal:  Indian J Dermatol        ISSN: 0019-5154            Impact factor:   1.494


  7 in total

1.  The clinical spectrum of epidermolysis bullosa simplex.

Authors:  H M Horn; M J Tidman
Journal:  Br J Dermatol       Date:  2000-03       Impact factor: 9.302

2.  Bart syndrome: the congenital localized absence of skin may follow the lines of Blaschko. Report of six cases.

Authors:  C Duran-McKinster; A Rivera-Franco; L Tamayo; M de la Luz Orozco-Covarrubias; R Ruiz-Maldonado
Journal:  Pediatr Dermatol       Date:  2000 May-Jun       Impact factor: 1.588

Review 3.  The pyloric atresia-junctional epidermolysis bullosa syndrome. Report of a case and review of the literature.

Authors:  G G Lestringant; S R Akel; K I Qayed
Journal:  Arch Dermatol       Date:  1992-08

4.  Genetic basis of Bart's syndrome: a glycine substitution mutation in type VII collagen gene.

Authors:  A M Christiano; B J Bart; E H Epstein; J Uitto
Journal:  J Invest Dermatol       Date:  1996-04       Impact factor: 8.551

5.  Congenital localized absence of skin and associated abnormalities resembling epidermolysis bullosa. A new syndrome.

Authors:  B J Bart; R J Gorlin; V E Anderson; F W Lynch
Journal:  Arch Dermatol       Date:  1966-03

Review 6.  Congenital localized absence of the skin as a manifestation of epidermolysis bullosa.

Authors:  M H Kanzler; B Smoller; D T Woodley
Journal:  Arch Dermatol       Date:  1992-08

7.  Bart's syndrome. Ultrastructure and genetic linkage.

Authors:  B Zelickson; K Matsumura; D Kist; E H Epstein; B J Bart
Journal:  Arch Dermatol       Date:  1995-06
  7 in total
  6 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.  Bart's Syndrome Associated Corpus Callosum Agenesis and Choanal Atresia.

Authors:  Muhammad Saeed; Anwar Ul Haq; Khaqan Qadir
Journal:  Iran J Child Neurol       Date:  2014

3.  A Case of Aplasia Cutis Congenita Type VI: Bart Syndrome.

Authors:  Yasmin Alfayez; Sahar Alsharif; Adel Santli
Journal:  Case Rep Dermatol       Date:  2017-08-03

4.  Bart's syndrome associated with a disorder of sexual differentiation: An atypical presentation in a Cameroonian newborn.

Authors:  Odette Berline Sigha; Ritha Mbono Betoko; Grace Anita Nkoro; Mireille Fossi Happi; Charlotte Eposse Ekoube; Benjamin Bertrand Kelbaba; Edgar Mandeng Ma Linwa; Emmanuel Armand Kouotou
Journal:  Clin Case Rep       Date:  2022-01-07

5.  Twin Neonates With Bart's Syndrome.

Authors:  Saleh Al-Gburi; Zainab Namuq
Journal:  Cureus       Date:  2022-01-18

6.  Type VI Aplasia Cutis Congenita: Bart's Syndrome.

Authors:  Ferit Kulalı; Ahmet Yagmur Bas; Yusuf Kale; Istemi Han Celik; Nihal Demirel; Sema Apaydın
Journal:  Case Rep Dermatol Med       Date:  2015-11-01
  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.