Global registry and database on craniofacial anomalies Report of a WHO Registry Meeting on Craniofacial Anomalies
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Global strategies to reduce the health care burden of craniofacial anomalies: report of WHO meetings on international collaborative research on craniofacial anomalies.
Although several significant research projects have arisen from international cooperation, especially in the field of genetics, these have been the exception rather than the rule. However, those of us who had the privilege and delight of participating in the World Health Organization meetings were struck by a common realization of the vast potential of systematic international cooperation. It i...
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Mutations in the AHDC1 gene are associated with the Xia-Gibbs syndrome (XGS), a sporadic genetic disorder characterised by developmental delay, intellectual disability, hypotonia, obstructive sleep apnoea, dysmorphic facial features, and cerebral malformations with plagiocephaly. Here we report the case of a 13-year-old Colombian female patient with a history of developmental delay, speech dela...
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Background and Objective: Congenital craniofacial anomalies emerge as changes in structure, function and metabolism at birth. This study aimed to identify congenital malformations of the face and different non-healed and healed craniofacial fractures and their epidemiology in people younger than 18 years in the province of Zanjan. Materials and Methods: This study was carried out on all urba...
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INTRODUCTION Hypospadias is a congenital abnormality of the penis, in which there is incomplete development of the distal urethra. There are numerous reports showing na increase of prevalence of hypospadias. Association of craniofacial malformations in patients diagnosed with hypospadias is rare. The aim of this study is to describe the association between hypospadias and craniofacial congenita...
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