Munis Dundar

Munis Dundar (Turkish: Munis Dündar) is a professor of Medical Genetics and Head of the Medical Genetics Department at Erciyes University, Kayseri, Turkey. He is founder and head of the Medical Genetics Department at Erciyes University and has carried out various administrative tasks since 1996. He defined four genetic syndromes in the medical literature: the “Dundar Syndrome”, “Dundar Acropectoral Syndrome”, “Scoliosis, Blindness and Arachnodactyly Syndrome” and “Multiple Congenital Abnormalities and Mental Retardation Syndrome”. He has taken part as project coordinator and assistant investigator in many research projects and has prepared articles published in international journals since 1995. He is the president of EBTNA (European Biotechnology Thematic Network Association) and representative from Turkey. He is also the editor-in-chief of The EuroBiotech Journal.

Munis Dundar
Born (1961-05-02) May 2, 1961
Estel
NationalityRepublic of Turkey
Alma mater
Children3
Awards
  • The most article on journals indexed by SCI award in Erciyes University (2003)
  • EBTNA service award (2011)
Websitemunisdundar.com
Notes
Web of Science H Index: 20, Cited Numbers: 2100

Research Interest: Basic Principle in the Genetic Diseases and Clinic Applications, Basic Principle in the Medical Genetics, Mendelian and Nonmendeilan Inheritance, Population Genetics, Dysmorphology, Chromosomal Diseases, Genetic Counseling, Prenatal Diagnosis Methods, Transgenic Mouse Generation and Biotechnology, Cytogenetics, Molecular Cytogenetics.

Professional memberships
  • 2009-2011/ President of Turkish Medical Genetics Association
  • Member of Medical Health Commission of Turkish Council of Higher Education
  • Advisory committee of Kocatepe Medical Journal
  • Co-editor of Journal of Molecular diagnosis
  • Advisory committee of Clinical Pediatric Journal of Turkey
  • Referee and Panelist of Project Evaluation Committee of TUBITAK
  • Advisory committee of Journal of Pediatric Neurology
  • 2007-2009/ Board member and 2nd president of Turkish Medical Genetics Association
  • 2002-2005/ Founder and Chairman of Medical School Graduated Students Association
  • Member of Experimental and Clinic Researches Association of Erciyes University
  • Board Member of European Society of Human Genetics
  • Member of British Society of Human Genetics
  • Member of European Cytogenetic Association
  • President of European Biotechnology Thematic Network Association[1]

Publications and Defined Syndromes

There are more than 150 articles in which Munis Dundar is corresponding or co-author including researches on new syndromes defined by himself:[2]

  • Dundar Syndrome, 1997
  • Dundar Acropectoral Syndrome, 2001
  • Blindness, Scoliosis and Arachnodactyly Syndrome 2008
  • Multiple Congenital Abnormalities and Mental Retardation 2012

All syndromes are in International Catalogs such as, Online Mendelian Inheritance in Man and Oxford Medical Databases.

Dundar Syndrome

Dundar et al. described patients with Mental Motor Retardation, ocular abnormality, dysmorphic facial appearance, long fingers, and distal arthrogryposis with severely adducted thumbs and clubfeet in Turkish family in 1997.[3][4][5]

Dundar Acropectoral Syndrome

In 2001 family with a distal limb and sternal abnormalities were reported by Dundar et al. This autosomal dominant disease signs which are syndactyly, preaxial polydactyly prominent and upper sternum were established in affected individuals. Dundar et al. (2001) noticed similarities with F syndrome[6] but significant differences proved otherwise.OMIM 605967

Scoliosis, Arachnodactyly and Blindness Syndrome

In 2008 Dundar et al. described Turkish family with dominantly-inherited blindness, scoliosis and arachnodactyly.[7]

Multiple Congenital Abnormalities and Mental Retardation Syndrome

Two brothers with abnormal neurological development, short height, pylorus stenosis, pectus excavatum, craniosynostosis, large ears, thin upper lip and bilateral cryptorchidism were reported by Dundar et al. in 2012. While investigating these symptoms were concluded that the summary of findings is not seen in known syndromes and because of non-affected parents who are siblings, this is an autosomal recessive inherited new syndrome.[8]

Books
  • Dündar M, Eds, "Modern Biyoteknoloji Ve Uygulamalar", Erciyes Üniversitesi Yayınları, Kayseri, 2010
  • Dündar M, Eds "Dismorfolojide Terimler Ve Tanımlar", Erciyes Üniversitesi, KAYSERİ, 2015 ISBN 978-605-85579-3-2
  • Dündar M, Eds. "Current Applications of Biotechnology", mgroup published, Kayseri, 2015
  • Dündar M, Eds. "Atlas of Dysmorphology and Diagnosis", mgroup published, Kayseri, 2015

Awards
  • Scientific Publication Award by Erciyes University, 2003
  • European Biotechnology Thematic Network Association service award, 2011

References
  1. "Archived copy". www.ebtna.net. Archived from the original on 23 November 2015. Retrieved 20 October 2015.CS1 maint: archived copy as title (link)
  2. Barthel, W.; Markwardt, F. (1975). "Dundar M[Author]". Biochemical Pharmacology. 24 (20): 1903–4. doi:10.1016/0006-2952(75)90415-3. PMID 20.
  3. Dundar, Munis; Demiryilmaz, Fatma; Demiryilmaz, Ilhan; Kumandas, Sefer; Erkilic, Kuddusi; Kendirci, Mustafa; Tuncel, Mehmet; Ozyazgan, Isilay; Tolmie, John L (27 June 2008). "An autosomal recessive adducted thumb-club foot syndrome observed in Turkish cousins". Clinical Genetics. 51 (1): 61–64. doi:10.1111/j.1399-0004.1997.tb02417.x. PMID 9084938.
  4. Dundar, M; Kurtoglu, S; Elmas, B; Demiryilmaz, F; Candemir, Z; Ozkul, Y; Durak, AC (September 2001). "A case with adducted thumb and club foot syndrome". Clinical Dysmorphology. 10 (4): 291–3. doi:10.1097/00019605-200110000-00012. PMID 11666007.
  5. Dündar, M; Müller, T; Zhang, Q; Pan, J; Steinmann, B; Vodopiutz, J; Gruber, R; Sonoda, T; Krabichler, B; Utermann, G; Baenziger, JU; Zhang, L; Janecke, AR (November 2009). "Loss of dermatan-4-sulfotransferase 1 function results in adducted thumb-clubfoot syndrome". American Journal of Human Genetics. 85 (6): 873–82. doi:10.1016/j.ajhg.2009.11.010. PMC 2790573. PMID 20004762.
  6. Dundar M, Gordon TM, Ozyazgan I, et al. (May 2001). "A novel acropectoral syndrome maps to chromosome 7q36". J. Med. Genet. 38 (5): 304–9. doi:10.1136/jmg.38.5.304. PMC 1734869. PMID 11333865.
  7. Dundar, M; Erkilic, K; Argun, M; Caglayan, AO; Comeglio, P; Koseoglu, E; Matyas, G; Child, AH (2007). "Scoliosis, blindness and arachnodactyly in a large Turkish family: is it a new syndrome?". Genetic Counseling (Geneva, Switzerland). 19 (3): 319–30. PMID 18990988.
  8. Dundar, M; Ozdemir, SY; Fryns, JP (2011). "A new syndrome: multiple congenital abnormalities and mental retardation in two brothers". Genetic Counseling (Geneva, Switzerland). 23 (1): 13–8. PMID 22611637.
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