Fatma SILAN, MD

 

Education:1) Istanbul University Cerrahpasa Medical Faculty Genetic Department.

            (Medical Genetic Specialist/1993-1996.)

2) Ege University Medical Faculty.             (Medical Doctor /1987-1993.)

Professional Experience:

·        Abant Izzet Baysal University(AIBU) Duzce Medical Faculty Medical Biology Department, Assistant Proffessor, 2000-

·         Istanbul Sisli Etfal City Hospital, Genetic Counselor 1996- 2000

·        Istanbul University Cerrahpasa Medical Faculty Genetic Department /1996-1993. Specialization education.

Administrative Mission

·        AIBU Duzce Medical Faculty  Medical Biology Department, Chairman

·        AIBU Medical Sciences Instutite Medical Biology and Genetic Department , Chairman

·        AIBU Duzce Medical Faculty  Education Committee member

·        Abant Izzet Baysal University, Duzce Medical Journal, Publication committee member

Lectures:

·        AIBU Duzce Medical Faculty  Medical Biology education

·        AIBU Duzce Medical Faculty  Medical Genetic education

·        AIBU Medical Sciences Instutite Medical Biology and Genetic Master program counselor

·        Cytogenetic (master program)

·        Molecular Basis of Genetic Diseases I, (master program)

·        Cytobiology (master program)

 

Publications:

  1. A new mutation of the fukutin gene in a non-Japanese patient with very severe and fatal abnormalities of the eye and brain as well as muscular dystrophy. Fatma SILAN, Mieko Yoshioka, Kazuhiro Kobayashi, Enver Simsek, Murat Tunc, Murat Alper, Meryem Cam, Aysel Guven, Yoji Fukuda, Moritoshi Kinoshita, Kenan Kocabay, Tatsushi Toda, Accepted for Annals Neurology
  2. Type 1Neurofibromatozis and Buphtalmus,Murat Kaya, Murat Tunç, Fatma SILAN, Gulderen Aktan,  Abant Izzet Baysal University Duzce Medical Faculty  Journal, 3:1, 2001, sf 29-32
  3. Isolated Hemihypertrophy Cases, Fatma SILAN, Kemal Ugurlu, Guner Karatekin. Abant Izzet Baysal University Duzce Medical Faculty  Journal, 2:2, 2000, sf 106-112
  4. Eritrocyte Glutathion , Glutathion peroksidase, Glutathion S-transferase  levels of Down Syndrome . Fatma SILAN, Mujgan Cengiz, Mehmet Seandn, Seniha Hacıhanefioglu, Abant Izzet Baysal University Duzce Medical Faculty  Journal, 2:1, 2000, sf40-44
  5. Malarya: Case Report. Ö.Salihoglu,  G Karatekin, N Kınalıada, Fatma SILAN, MY Esen, A. Nuhoglu. Abant Izzet Baysal University Duzce Medical Faculty  Journal, 2:1, 2000, sf 118-121
  6. Antioksidant system in Down Syndrome, a possible role in cataractogenesis. Z Suyugul, M Cengiz, M Seven, Fatma Sılan, B Tuysuz, S Hacıhanefioglu, A Cenani. Turkish Journal of Medical Research a Publishing Organ of Istanbul University
  7. Genetic Diseases and Hair; Fatma SILAN, Galenos May 1999, sf 15-17
  8. “A rare Turner Syndrome variant case with X/Otosom Translocation” S Palanduz, S Özturk, K Çefle, B karaman, Fatma Sılan, G Tutkan, D Ustek, A Uçur, S Basaran. Turkish Medical Association Journal, accepted
  9. “Two siblings with XY Gonodal Disgenezis”S Palanduz, K Çefle, S Özturk, F Aral, N Özbey, MA Karan, H Erkal, Fatma SILAN, S Moldovalılar. Turkish Medical Association Journal, accepted

Posters:

1.      “The first Non-Japanese case of Fukuyama Type Congenital Muskuler Dystrophy and a Novel Fukutin Mutation”, Fatma SILAN, Kenan Kocabay, Tatsushi Toda. V. National Prenatal Diagnosis and Genetic Congress, October 2002, Konya

2.      “Incontinentia Pigmenti and NEMO Mutation in a Turkish Family“ Fatma SILAN, Ilker Aydogan, Tziano Bardaro, Ayse Kavak, Michele D’urso, I. National Diagnostic Molekuler Genetic Congress, April 2002, Adana

3.      “Protective effect of melatonin at Streptozotocin diabetic rats” Özlem Yavuz, Meryem Cam, Neslihan Bukan, Aysel Guven, Fatma Sılan. II. National Clinic Biochemistry Congress, 31 October 4 November 2001,

4.      “Non Hodgkin Lenfoma and Ear Hipoplasia. Colloid Milium or Lignous Conjunktivitis?” Aysa Kavak, Murat Kaya, Murat Alper, Meryem Çam, Nesimi Buyukbabani, Abdurrahman Bilen, Fatma SILAN. XV. Prof. Dr.Lutfu Tat Symposium. 30 September-4 October 2001

5.      “Ophtalmologic Findings of Hallerman Streiff Syndrome” Murat Tunç, Fatma Sılan, Gulderen Aktan, Murat Kaya, Abdurrahman Bilen. TOD XXXIV. National Oftalmoloji Congress. 30 Eylul-4 October 2000.

6.      “Genetics of Premature Graying” Fatma SILAN, Esra Arpag, Adem Koslu XXVI. Semaine Medicale Balkanique, 7-10 May 2000,  Archiands of the Balkan Medical Union, Vol. 35, Supp.1, March2000, pp.27-28’

7.      “Brakidactili Type B, Hydrosefali, Dental Anomalies and Kifoskolyoz: Case Report” Fatma Sılan, B Tuysuz, Andrew Wilkie. IV. National Prenatal Diagnosis and Genetic Congress, 3-6 May 2000

8.      “A rare Turner Syndrome variant case with X/Otosom Translocation” S Palanduz, S Özturk, K Çefle, B Karaman, Fatma Sılan, G Tutkan, D Ustek, A Uçur, S Basaran. Istanbul Medical Faculty  14. Congress May 1998

9.      “Two siblings with XY Gonodal Disgenezis” S Palanduz, K Çefle, S Özturk, F Aral, N Özbey, MA Karan, H Erkal, Fatma SILAN, S Moldovalılar Istanbul Medical Faculty  14. Congress May 1998

10.  “Eritrocyte Glutathion , Glutathion peroksidase, Glutathion S-transferase  levels of Down Syndrome Children” 4. National Medical Biology Congress June 1996 Izmir

11.  “Antioxidant System in Down Syndrome: A Possible Role in Cataractogenesis” Z Suyugul, M Cengiz, M Seandn, Fatma Sılan, B Tuysuz, S Hacıhanefioglu, A Cenani. 2nd Balkan Meeting on Human Genetics September 1996

Congress  and Certificate Programs:     

1.      V. National Prenatal Diagnosis and Genetic Congress, October 2002, Konya

2.      I. National Diagnostic Molekuler Genetic Congress, 18-22 April 2002, Adana

3.      XXVI. Semaine Medicale Balkanique, 7-10Mayıs 2000

4.      IV. National Prenatal Diagnosis and Genetic Congress, 3-6 May 2000

5.      Istanbul Medical Faculty  14. Congress May 1998

6.      4.National Medical Biology Congress June Izmir

7.      2nd Balkan Meeting on Human Genetics September 1996

8.      2nd Asian-European Workshop on Inborn Errors of Metabolism. 29th August – 2nd September, 1994

9.      Human Genom Project: New Perspectiands and Applications in Molecular Medicine Workshop. Bilkent July 1997

 

Project Management

“Phenotypic Evaluation and DNA Banking at Autosomal Recessive and Syndromic Cases of Childhood Deafness.” Project No: 2002.07.01.119, Abant Izzet Baysal University Scientific Research Fund.