Neurology
Study Course Implementer
Residency Speciality
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About Study Course
Objective
Learning Outcomes
Knowledge
1.During the study course, medical genetics resident acquires basic knowledge of general neurology.
Skills
1.As a result of this study course, medical genetics resident will be able to assess the overall condition of a patient, physical indicators; able to assess the results of laboratory and radiologic exam results, reason on illness prognosis, treatment and tactics of further care.
Competences
1.Resident’s knowledge corresponds the overall understanding of development and examination of a neurology. The resident is able to create an examination plan appropriate for setting the diagnosis, to prescribe examinations. Knowledge of the given issue is sufficient to understand its essence, to diagnose and provide with emergency assistance, when necessary, to realize diagnostics, treatment, and preventive measures under the guidance of a specialist.
Assessment
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Bibliography
Required Reading
Gross, S. J. Introduction to Perinatal Disorders and Reproductive Genetics. In Emery and Rimoin’s Principles and Practice of Medical Genetics and Genomics, 2022
Milunsky, A., & Milunsky, J. M. Genetic Disorders and the Fetus: Diagnosis, Prevention and Treatment: 6th Edition. In Genetic Disorders and the Fetus: Diagnosis, Prevention and Treatment, 2010
Leung, P. C. K., & Qiao, J. Human reproductive and prenatal genetics. In Human Reproductive and Prenatal Genetics, 2018
Harper, J. C.. Preimplantation genetic diagnosis. In Preimplantation Genetic Diagnosis, 2nd Edition, 2009
DiMaio, M. S., Fox, J. E., & Mahoney, M. J. Prenatal Diagnosis: Cases and Clinical Challenges. In Prenatal Diagnosis: Cases and Clinical Challenges, 2010
Paladini, D., & Volpe, P. Ultrasound of Congenital Fetal Anomalies. In Ultrasound of Congenital Fetal Anomalies, 2018
Stevenson, R., Hall, J., Everman, D., & Solomon, B. (Eds.), Human Malformations and Related Anomalies. Oxford, UK: Oxford University Press, 2015
Harper, P. Practical Genetic Counselling. 7th edition. CRC Press, 2011
Cassidy, S., Allanson, J. Management of Genetic Syndromes. Wiley-Blackwell, 2010
Firth, H., Hurst, J. Oxford Desk Reference Clinical Genetics. Oxford, 2007
Read, A, Donnai, D. New clinical Genetics. A guide to Genomics Medicine. Scion, 2021
Dhar, S., Sandesh, N, Eble, T. Hanbook of Clinical adult Genetics and genomics. Elssevier, 2020
Reardson, W. The Bedside Dysmorhologist. Oxford, 2016
Jones, Kenneth L, Marilyn C. Jones, and Miguel . Campo. Smith's Recognizable Patterns of Human Malformation, 2013
Norton, M.E., Scoutt, L., Feldstein, V. Callens Ultrasonography in Obstretics And Gynecology. Elsevier.2017
Hollak, C., Lachmann, R. Inherited Metabolic Disease in Adults.Oxford, 2016
Saudubray, F., Van den Berghe, W. Inbron Metabolic diseases. Springer, 2016
Katirji, B., Kaminski, J.H, Ruff, R.L. Neuromuscular Disorders in Clinical Paractice Vol1., Vol2.Springer, 2014
Govidan, R., Devarakonda, S. Cancer Genomics for the Clinician. Springer, 2019
Hogge, A., Wilkins, I., Hills, L., Cohlan B. Sanders Structural Fetal Abnormalities. McGraw Hill Education, 2017
Other Information Sources
OMIM.https://omim.org
Genereviews. https://www.ncbi.nlm.nih.gov/books/NBK1116/
Phenomizer. HPO. https://hpo.jax.org/app/tools/phenomizer
Varsome. https://varsome.com/
Reprotox. https://www.reprotox.org/
Metagene. https://www.metagene.de/
Vademecum Metabolicum. http://www.vademetab.org/
Metabolic Emergency Protocol. https://www.emergencyprotocol.net/
Treat NMD. https://treat-nmd.org/
NCCN Guidelines. https://www.nccn.org/guidelines/guidelines-detail?category=2&id=1503