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Published on: August 20, 2019
A rare X-linked inherited mucocutaneous syndrome in two siblings
1Department of Paediatrics, Faculty of Medicine, Universiti of Malaya, 50603 Kuala Lumpur. leeai@um.edu.my
Abstract:
We report on an 11 year-old boy with dyskeratosis congenita who presented with dystrophic nails, dysphagia, hyperpigmentation and oral leukoplakia. He had a brother who died 14 years earlier with similar presenting symptoms and aplastic anaemia. Genetic studies of our patient demonstrated the presence of a DKC1 mutation and confirmed our diagnosis. Further genetic screening revealed that his mother and one of his four sisters are heterozygous for the same mutation.
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