BMJ case reports · 2012
A child with bone fractures and dysmorphic features: remember of pycnodysostosis and craniosynostosis.
Клинический случайСтатьяНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Berenguer Alberto, Freitas António Pedro, Ferreira Gomes, Nunes José Luis
Аннотация
Accidental bony injuries are common in children. Children may also present with bony injuries following non-accidental injuries. Pathological fractures, though extremely rare, are an important entity and constitute fractures that occur in abnormal bones, usually after minor trauma. Pycnodysostosis is a rare skeletal dysplasia characterised by a clinical phenotype that includes short stature, skull deformities, osteosclerosis, acroosteolysis and bone fragility. Often the disease is diagnosed at an early age as a result of the investigation of short stature. However, the diagnosis is sometimes delayed and must be considered in any child with a history of recurrent or multiple bone fractures and dysmorphic features. The purpose of this report is to describe the clinical, radiological and genetic issues of a 9-year-old girl with a long history of multiple bone fractures. She had been subjected to safeguarding investigations previously and was identified to have dysmorphic features diagnosed as pycnodysostosis associated with craniosynostosis.
Предметные рубрики MeSH
Abnormalities, MultipleCathepsin KChildChromosomes, Human, Pair 1Craniofacial AbnormalitiesCraniosynostosesDNA Mutational AnalysisFaciesFemaleFractures, SpontaneousHumansImage Processing, Computer-AssistedImaging, Three-DimensionalMuscular AtrophyOsteosclerosisPycnodysostosisSkullTomography, X-Ray Computed