Transient monoparesis after blade plate removal in a Hutchinson–Gilford progeria syndrome patient: a case report
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منابع مشابه
A Case Report of Hutchinson-Gilford Progeria Syndrome
Hutchinson-Gilford Progeria Syndrome (HGPS), a rare genetic condition occurs one in every 8 million live births. HGPS is characterized by premature aging in various organs. The average survival rate of the affected patients is 13 years, and their most common causes of death are myocardial infarction and stroke. This disease occurs due to a gene mutation in the chromosomes of the patient. There ...
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ژورنال
عنوان ژورنال: Journal of Pediatric Orthopaedics B
سال: 2009
ISSN: 1060-152X
DOI: 10.1097/bpb.0b013e32832ab928