Genetic Analysis in First Indonesian CHARGE

Syndrome Patient
Student Exchange Program Report
Submitted as a Partial Fulfillment of the Requirements for Taking Final
Examination

Laboratory of Neurovascular Unit and Cognitive Disorders

Submitted by:

Muhammad Abror
114170041

FACULTY OF MEDICINE
SWADAYA GUNUNG JATI UNIVERSITY
CIREBON

2018
 Student Exchange Program Report

Genetic Analysis in first Indonesian CHARGE Syndrome Patient

Muhammad Abror
114170041

Submitted as a Partial Fulfillment of the Requirements for Taking Final

Examination

Approved:

Poitiers, February 2018

Main supervisor Supervisor

Vincent Thoreau, Ph.D Gara S. Brajadenta, MD, M.Med.Sc

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 PREFACE
It is a great opportunity for me to join Student Exchange Program and
learn about molecular biology in Université de Poitiers, France. In the
accomplishment of this student exchange program, I am submitting a report on
‘Genetic Analysis in first Indonesian CHARGE Syndrome Patient’. Doing
this report helped me to enhance my knowledge regarding the work in detecting
some mutation related to the CHARGE Syndrome. Through this report, I come to
know the importance of mutation detection in CHD7 gene.
With this report, I thank to my supervisor Dr. Vincent Thoreau, Ph.D and
Gara Samara Brajadenta, MD for their help in the process of making this study
report. Thanks to Prof. Gerard Mauco and Prof. Guylene Page to give me the
chance to study in Université de Poitiers. And big thanks for Faculty of Medicine
Swadaya Gunung Jati University especially for The Dean Catur Setiya
Sulistiyana, MD, M.Med.Ed who give me a big chance to be enrolled in this
student exchange program at University of Poitiers, France.

Poitiers, February 2018

Author

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