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Aghabozorgi, Amirsaeed, Ahangari, Najmeh, Mobini, Moein, Vakili, Rahim, Doosti, Mohammad, Vakili, Saba, Karimiani, Ehsan. (1401). A Novel Heterozygous ACAN Variant in an Iranian Family with Short Stature: A Case Report. , 10(9), 16729-16737. doi: 10.22038/ijp.2022.63946.4859
Amirsaeed Sabeti Aghabozorgi; Najmeh Ahangari; Moein Mobini; Rahim Vakili; Mohammad Doosti; Saba Vakili; Ehsan Ghayoor Karimiani. "A Novel Heterozygous ACAN Variant in an Iranian Family with Short Stature: A Case Report". , 10, 9, 1401, 16729-16737. doi: 10.22038/ijp.2022.63946.4859
Aghabozorgi, Amirsaeed, Ahangari, Najmeh, Mobini, Moein, Vakili, Rahim, Doosti, Mohammad, Vakili, Saba, Karimiani, Ehsan. (1401). 'A Novel Heterozygous ACAN Variant in an Iranian Family with Short Stature: A Case Report', , 10(9), pp. 16729-16737. doi: 10.22038/ijp.2022.63946.4859
Aghabozorgi, Amirsaeed, Ahangari, Najmeh, Mobini, Moein, Vakili, Rahim, Doosti, Mohammad, Vakili, Saba, Karimiani, Ehsan. A Novel Heterozygous ACAN Variant in an Iranian Family with Short Stature: A Case Report. , 1401; 10(9): 16729-16737. doi: 10.22038/ijp.2022.63946.4859

A Novel Heterozygous ACAN Variant in an Iranian Family with Short Stature: A Case Report

Journal of Pediatric Perspectives
مقاله 13، دوره 10، شماره 9، آذر 2022، صفحه 16729-16737    اصل مقاله (421.09 K)
نوع مقاله: case report
شناسه دیجیتال (DOI): 10.22038/ijp.2022.63946.4859
نویسندگان
Amirsaeed Sabeti Aghabozorgi1؛ Najmeh Ahangari2؛ Moein Mobini3؛ Rahim Vakili4؛ Mohammad Doosti5؛ Saba Vakili* 3؛ Ehsan Ghayoor Karimiani* 6
1Medical Genetics Research Center, Medical School, Mashhad University of Medical Sciences, Mashhad, Iran
2Innovative Medical Research Center, Islamic Azad University, Mashhad, Iran. Department of Medical Genetics, Next Generation Genetic Polyclinic, Mashhad, Iran.
3General Paediatrics, Evelina London Children’s Hospital, Guy’s and St. Thomas’ National Health Service Foundation Trust, London, United Kingdom
4Department of Pediatric Endocrinology and Metabolism, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran
5Department of Medical Genetics, Next Generation Genetic Polyclinic, Mashhad, Iran
6Innovative Medical Research Center, Islamic Azad University, Mashhad, Iran. Department of Medical Genetics, Next Generation Genetic Polyclinic, Mashhad, Iran. Molecular and Clinical Sciences Institute, St. George’s, University of London, London, United Kingdom.
چکیده
Background: Short stature is estimated to account for half of the new visits to pediatric endocrine practices. Therefore, evaluating its underlying causes seems essential in order to choose the best treatment. Recently, some studies revealed the impact of ACAN, which encodes for aggrecan, mutations on growth ranging from mild idiopathic short stature to severe skeletal dysplasia.
Methods: Here, we describe clinical and molecular characteristics of an Iranian family with short stature using exome sequencing and co-segregation analysis through Sanger sequencing.
Results: A novel variant of ACAN mutation c.1604delG (p.Arg535fs) was identified in the heterozygote pattern which was confirmed through co-segregation analysis in family members.
Conclusion: We have found a novel variant within the ACAN gene in association with insignificant bone abnormality without a high incidence of familiar bone malformation. In order to achieve better clinical outcomes, we suggest genetic testing at an earlier age and also long-term GH treatment for children who are at risk of ACAN mutations. Children who are born small considering their gestational age, or who have persistent short stature, advanced bone age, midfacial hypoplasia, joint problems, or broad toes, can be candidates for ACAN sequencing.
کلیدواژه‌ها
ACAN؛ Molecular Diagnostics؛ Skeletal dysplasia؛ Pediatrics
مراجع
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