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The de Barsy syndrome

We report a child with de Barsy syndrome, which is a very rare, genetically transmitted clinical entity associated with mental and growth retardation, severe cutis laxa, joint laxity and various ocular and skeletal system findings. The patient was operated to treat her orthopedic disabilities...

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Главные авторы: M Arazi, M I Kapicioğlu, M Mutlu
Формат: Artigo
Язык:Inglês
Опубликовано: Hacettepe University Institute of Child Health 2001-01-01
Серии:The Turkish Journal of Pediatrics
Online-ссылка:https://turkjpediatr.org/article/view/3023
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