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Literature DB >> 25685377

Bart syndrome with ear malformation.

Ahmed Omran¹, Dalia Elimam¹, Reem A E Mobarak¹, Mohammed Ibrahim¹, Sonia El-Sharkawy¹.

Abstract

Entities: Disease

Year: 2015 PMID： 25685377 PMCID： PMC4318598

Source DB: PubMed Journal: Sultan Qaboos Univ Med J ISSN： 2075-051X

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11 in total

1. 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

2. Genetic linkage between the collagen VII (COL7A1) gene and the autosomal dominant form of dystrophic epidermolysis bullosa in two Dutch kindreds.

Authors: N A Gruis; J N Bavinck; P M Steijlen; J G van der Schroeff; A van Haeringen; R Happle; E Mariman; S E van Beersum; J Uitto; B J Vermeer
Journal: J Invest Dermatol Date: 1992-11 Impact factor: 8.551

3. Basic science of epidermolysis bullosa and diagnostic and molecular characterization: Proceedings of the IInd International Symposium on Epidermolysis Bullosa, Santiago, Chile, 2005.

Authors: Ellen G Pfendner; Anna Bruckner; Paulette Conget; Jemima Mellerio; Francis Palisson; Anne W Lucky
Journal: Int J Dermatol Date: 2007-08 Impact factor: 2.736

Bart syndrome with ear malformation.

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

2. Genetic linkage between the collagen VII (COL7A1) gene and the autosomal dominant form of dystrophic epidermolysis bullosa in two Dutch kindreds.

3. Basic science of epidermolysis bullosa and diagnostic and molecular characterization: Proceedings of the IInd International Symposium on Epidermolysis Bullosa, Santiago, Chile, 2005.

4. Bart's syndrome associated with pyloric and choanal atresia.

5. Bart syndrome.

6. Prenatal diagnosis of epidermolysis bullosa letalis.

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

8. Prenatal diagnosis for severe inherited skin disorders: 25 years' experience.

Review 9. Aplasia cutis congenita: a clinical review and proposal for classification.

10. Clinical phenotype of Bart's syndrome seen in a family with dominant dystrophic epidermolysis bullosa.