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									<identifier>oai:www.peertechzpublications.org:10.17352/amm.000030</identifier>
									<datestamp>2023-04-18</datestamp>
									<setSpec>PTZ.AMM:VOL7</setSpec>
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									<oai_dc:dc xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:mml="http://www.w3.org/1998/Math/MathML" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
										<dc:title>
										Spondyloepipheseal dysplasia tarda
										</dc:title><dc:creator>Raisa Altaf</dc:creator><dc:creator> Rabiya Siraj</dc:creator><dc:creator> Ramsha Fatima Qureshi</dc:creator><dc:creator> Uzma Panhwer</dc:creator><dc:creator> Hina Naseer</dc:creator><dc:creator>Khansa Abro</dc:creator><dc:description>&lt;p&gt;Skeletal disorders are common entities that we encounter in our daily practice. Their early diagnosis is key to proper management and genetic counselling. Spondyloepiphyseal dysplasia is one such disorder. It is a genetic bone deformity that affects the spine, proximal epiphysis and pelvis. The disease is either manifested at birth or during adolescence therefore given the terms SED congenita or SED tarda. Patients with SED present with variable features including short height, short neck, club foot, cleft palate, kyphoscoliosis or lordotic abnormalities. We also present a case of an 11-year-old boy who presented to us with complaints of stunted growth and abnormal posture and underwent radiological imaging.&lt;/p&gt;</dc:description>
										<dc:publisher>Annals of Musculoskeletal Medicine - Peertechz Publications</dc:publisher>
										<dc:date>2023-04-18</dc:date>
										<dc:type>Case Report</dc:type>
										<dc:identifier>https://doi.org/10.17352/amm.000030</dc:identifier>
										<dc:language>en</dc:language>
										<dc:rights>Copyright © Raisa Altaf et al.</dc:rights>
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