Veidlapa Nr. M-3 (8)

Study Course Description

Child Psychiatry

Main Study Course Information

Course Code

RGN_003

Branch of Science

Clinical medicine; Medicinal Genetics

ECTS

4.05

Target Audience

Medicine

LQF

Level 8

Study Course Implementer

Course Supervisor

Daiga Mūrmane

Residency Speciality

Speciality

Medical Geneticist

Supervisor of Medical Speciality

Daiga Mūrmane

Contacts

About Study Course

Objective

To introduce the medical genetics resident to the most common problems encountered in a child and adolescent psychiatry clinic, differential diagnostics and treatment options for common childhood diseases.

Learning Outcomes

Knowledge

1.During the study course, medical genetics resident acquires basic knowledge of general paediatrics and especially a child and adolescent psychiatry.

Skills

1.As a result of this study course, medical genetics resident will be able to assess the overall condition of a child or a adolescent, physical indicators and psychomotor development; 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 child or a adolescent. 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

Individual work

Title	% from total grade	Grade
1. Individual work	-	-

Examination

Title	% from total grade	Grade
1. Examination	-	-

Study Course Theme Plan

FULL-TIME

Part 1

Seminar

Modality	Location
-	-

Topics

Seminar

Modality	Location
-	-

Topics

Seminar

Modality	Location
-	-

Topics

Total ECTS (Creditpoints):

4.05

Number of Residency Seminars:

Length (weeks):

Final Examination:

Residency exam (Theory and practice)

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

Twining’s Textbook of Fetal Abnormalities. In Twining’s Textbook of Fetal Abnormalities, 2015

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

10.

Cassidy, S., Allanson, J. Management of Genetic Syndromes. Wiley-Blackwell, 2010

11.

Firth, H., Hurst, J. Oxford Desk Reference Clinical Genetics. Oxford, 2007

12.

Read, A, Donnai, D. New clinical Genetics. A guide to Genomics Medicine. Scion, 2021

13.

Dhar, S., Sandesh, N, Eble, T. Hanbook of Clinical adult Genetics and genomics. Elssevier, 2020

14.

Jones, Kenneth L, Marilyn C. Jones, and Miguel. Campo. Smith's Recognizable Patterns of Human Malformation, 2013

15.

Norton, M.E., Scoutt, L., Feldstein, V. Callens Ultrasonography in Obstretics And Gynecology. Elsevier, 2017

16.

Hogge, A., Wilkins, I., Hills, L., Cohlan B. Sanders Structural Fetal Abnormalities. McGraw Hill Education, 2017

17.

Hollak, C., Lachmann, R. Inherited Metabolic Disease in Adults.Oxford, 2016

18.

Saudubray, F., Van den Berghe, W. Inbron Metabolic diseases. Springer, 2016

19.

Katirji, B., Kaminski, J.H, Ruff, R.L. Neuromuscular Disorders in Clinical Paractice Vol1., Vol.2, Springer, 2014

20.

Govidan, R., Devarakonda, S. Cancer Genomics for the Clinician. Springer, 2019

21.

Reardson, W. The Bedside Dysmorhologist. Oxford, 2016

Other Information Sources

OMIM. https://omim.org

Orphanet. https://www.orpha.net/consor/cgi-bin/index.php

Phenomizer. HPO. https://hpo.jax.org/app/tools/phenomizer

Varsome. https://varsome.com/

Vademecum Metabolicum. http://www.vademetab.org/

Metabolic Emergency Protocol. https://www.emergencyprotocol.net/

NDC. https://neuromuscular.wustl.edu/

Treat NMD. https://treat-nmd.org/

NCCN Guidelines. https://www.nccn.org/guidelines/guidelines-detail?category=2&id=1503

10.

Genereviews. https://www.ncbi.nlm.nih.gov/books/NBK1116/

11.

Metagene. https://www.metagene.de/

12.

Reprotox. https://www.reprotox.org/