Poster Presentations

Student Posters

STUD 1. (student)

Awareness About Folic Acid Uses And Effects Among Medical Students In Ukraine

Mazan А.(1), Savkiv D.(1)

(1) Department of Children’s Diseases and Paediatric Surgery I. Horbachevsky Ternopil National Medical University, Ternopil, Ukraine

STUD 2. (student)

Awareness about folic acid and its effects among pregnant women in Western Ukraine

Jasinska J.(1), Koval A.-M.(1)

(1) Department of Children’s Diseases and Pediatric Surgery, Ukraine

STUD 4. (student)

Craniosynostosis as an additional feature of chromationopathies

Adamek Z.(1), Larysz D.(2), Jamsheer A.(3,4), Bukowska-Olech E.(3,4)

(1) Medical student, Poznan University of Medical Sciences, Poznan, Poland; (2) Department of Head and Neck Surgery for Children and Adolescents, University of Warmia and Mazury in Olsztyn, Olsztyn, Poland; (3) Department of Medical Genetics, Poznan University of Medical Sciences, Poznan, Poland; (4) These two authors contributed equally to this work

STUD 5. (student)

Women’s knowledge on congenital malformations and care for children with disabilities: A qualitative study from Pune district, India

Medhekar A.(1), Dhamdhere D.(1), Kar A.(1)

(1) Birth Defects and Childhood Disability Research Centre, Pune, India

STUD 6. (student)

Congenital disability in children under five years of age in India and access to health and welfare services

Chutke A.(1), Kar A.(1,2)

(1) Interdisciplinary School of Health Sciences, Savitribai Phule Pune University, Pune, Maharashtra, India; (2) Birth Defects and Childhood Disability Research Centre, Pune, Maharashtra, India

STUD 7. (student)

Porencephaly type I in children presenting pathogenic mutations in the COL4A1 gene

Skulimowski B.(1), Janiszewska M.(1), Winczewska-Wiktor A.(2), Steinborn B.(2), Badura-Stronka M.(1,3), Monies D.(4,5,6)

(1) Chair and Department of Medical Genetics, University of Medical Sciences, Poznan, Poland; (2) Chair and Department of Developmental Neurology, University of Medical Sciences, Poznan, Poland; (3) Centers of Medical Genetics Genesis, Poznan, Poland; (4) Department of Genetics, King Faisal Specialist Hospital and Research Centre, Saudi Arabia; (5) Saudi Human Genome Program, King Abdul-Aziz City for Science and Technology, Saudi Arabia; (6) Saudi Diagnostic Laboratories, King Faisal Specialist Hospital and Research Centre, Saudi Arabi

STUD 8. (student)

Clinical aspects of facial dysostoses

Adamek Z.(1), Materna-Kiryluk A.(2) Jamsheer A.(2,3), Bukowska-Olech E.(2,3)

(1) Medical student, University of Medical Sciences, Poznan, Poland; (2) Department of Medical Genetics, University of Medical Sciences, Poznan, Poland; (3) These two authors contributed equally to this work

STUD 9. (student)

Novel pathogenic variants and clinical features of syndromes associated with the GLI3 gene

Glista F.(1), Szymczak A.(1), Jamsheer A.(2,3), Bukowska-Olech E.(2,3)

(1) Medical student, University of Medical Sciences, Poznan, Poland; (2) Department of Medical Genetics,University of Medical Sciences, Poznan, Poland; (3) These two authors contributed equally to this work

STUD 10. (student)

EUROlinkCAT study on survival and morbidity among European children with Klinefelter syndrome

Rud Andersen A-L(1), EUROlinkCAT study group

STUD 11. (student)

Social limitations related to the COVID-19 epidemic and the work structure of associations of patients with rare diseases and their families – the pilot study

Pol M.(1), Milska-Musa K.A.(1), Lipska-Ziętkiewicz B.S.(2,3)

(1) Department of Quality of Life Research, Faculty of Health Sciences with the Institute of Maritime and Tropical Medicine, Medical University of Gdansk, Poland; (2) Rare Diseases Centre, Medical University of Gdansk, Poland; (3) Clinical Genetics Unit, Department of Biology and Medical Genetics, Medical University of Gdansk, Poland

STUD 12. (student)

The current state of genetic care for children with congenital anomalies in Wielkopolska province - data from the Polish Registry of Congenital Malformations (PRCM)

Andrzejewska A.(1), Nowak B.(1), Czarny J.(1), Dzierla J.(1), Zawileński M.(1), Wiśniewska K.(2), Glazar R.(3), Wiśniewska M.(4), Walkowiak A.(3), Latos-Bieleńska A.(4)

(1) Student Research Group of Medical Genetics, Chair and Department of Medical Genetics, University of Medical Sciences, Poznan, Poland; (2) Epidemiology Unit, Department of Preventive Medicine, University of Medical Sciences, Poznan, Poland; (3) Medical Genetics Center Genesis, Poznan, Poland; (4) Chair and Department of Medical Genetics, University of Medical Sciences, Poznan, Poland

STUD 13. (student)

Treatment challenges of severe congenital hydrocephalus in India

Budihal B.(1)

(1) Third-year medical student, BGS Global Institute of Medical Sciences, Bangalore, India

STUD 14. (student)

Cardiac arrhythmias after the closure of Secundum Atrial Septal defect (ASD II)

Mantiuk P.(1), Nikitiuk B.E.(1), Bowtruczuk A.(1), Bossowski A.(1), Bieganowska K.(2), Miszczak-Knecht M.(2)

(1) Department of Pediatrics, Endocrinology, Diabetology with Cardiology Division, Medical University of Bialystok, Poland; (2) Department of Cardiology in The Children&actue;s Memorial Health Institute in Warsaw, Poland

STUD 15. (student)

Identification of the molecular background of hypophosphatemic rickets in polish patients

Smuszkiewicz M.(1), Sowińska-Seidler A.(1)*, Jamsheer A.(1,2)*

(1) Department of Medical Genetics, University of Medical Sciences, Poznan, Poland; (2)Centers for Medical Genetics Genesis, Poznan, Poland; *Sowińska-Seidler A. and Jamsheer A. are both senior authors

STUD 16. (student)

An unusual case of 18 trisomy in the usual world – follow-up of a 4-year-old boy with Edwards Syndrome

Bałdyga P.(1), Berk K.(1,2)

(1) Medical University of Bialystok, Faculty of Medicine with the Division of Dentistry and Division of Medical Education in English; (2) University Oncology Center Medical University of Bialystok Clinical Hospital, Department of Clinical Genetics, Poland

This project has received funding from the European Union’s Horizon 2020 research and innovation programme under grant agreement No. 733001
The views presented here are those of the authors only, and the European Commission is not responsible for any use that may be made of the information presented here.
Projekt EUROlinkCAT otrzymał finansowanie z Unii Europejskiej "Horyzont 2020", Program badań i innowacji, umowa nr 733001.
Przedstawione tutaj poglądy są wyłącznie poglądami autorów, a Komisja Europejska nie ponosi odpowiedzialności za jakiekolwiek wykorzystanie przedstawionych tutaj informacji.

updated: 2022-04-06