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Schmid type metaphyseal chondrodysplasia is an autosomal dominant genetic disease. MCDS is a rare disorder and the presented case, to our knowledge, is the only Polish case with a confirmed and novel mutation of COL10A1 gene. Since the girl reached the age of 2 years and 7 months, she has been applied a systematic neurodevelopmental physiotherapy influencing the posture. The aim of the research was...
Introduction: Cerebral palsy is a great and serious medical problem. There are no effective ways of its treatment which is the main reason of constant research into successful therapeutical methods of rehabilitation. Nowadays, the rehabilitation is based on neurodevelopmental methods which are the most effective and friendly for children. Therefore, it is important to find an extensive approach towards...
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