Junctional epidermolysis bullosa associated with congenital localized absence of skin, and pyloric atresia in two newborn siblings

Author:

Puvabanditsin Surasak,Garrow Eugene,Kim Dae Un,Tirakitsoontorn Pornchai,Luan Jennifer

Publisher

Elsevier BV

Subject

Dermatology

Reference22 articles.

1. Symmetrical congenital skin defects in sibs, abstracted;Swinburne;Arch Dis Child,1968

2. Atresia de piloro en un recien nacido con epidermolisis ampollosa;Teran;Bol Catedra Pediatr (Madrid),1972

3. Congenital localized absence of skin and associated abnormalities resembling epidermolysis bullosa;Bart;Arch Dermatol,1966

4. The pyloric atresia- junctional epidermolysis bullosa syndrome;Lestringant;Arch Dermatol,1992

5. Ultrastructural findings in epidermolysis bullosa;Smith;Arch Dermatol,1993

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1. Junctional Epidermolysis Bullosa in a 30-day-old Infant: A Case Report;JOURNAL OF CLINICAL AND DIAGNOSTIC RESEARCH;2023

2. Epidermolysis bullosa: Pediatric perspectives;Current Pediatric Reviews;2021-05-25

3. Congenital Gastric Anomalies;Esophageal and Gastric Disorders in Infancy and Childhood;2017

4. Age and etiology of childhood epidermolysis bullosa mortality;Journal of Dermatological Treatment;2014-05-15

5. Inherited epidermolysis bullosa: clinical and therapeutic aspects;Anais Brasileiros de Dermatologia;2013-04

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