MUDr. Dagmar Raskova
pediatrics and medical genetics
pediatrics and medical genetics
Overview
Country, City
Czechia, Prague
Health facility
Gennet Clinic Letna Prague
Medical unit
Department of genetics
About the doctor
Skills & Expertise
genetics
medical genetics
hearing
hearing loss
gene
pediatrics
prenatal diagnosis
hereditary
prenatal
hereditary hearing loss
gene mutations
strc gene
dna
deafness
chromosome
heterozygosity
cataracts
gjb2 gene
kidney
slc26a4 mutations
bilateral cataracts
slc26a4
gjb6
congenital deafness
genetic conditions
prelingual deafness
pallisterkillian syndrome
6q deletions
dfnb16
ultrasound findings
ring chromosome
abnormal ultrasound
strc gene mutations
infant
retinal
pregnancy
polycystic
autosomal
sensorineural hearing loss
treacher collins syndrome
nonsyndromic hearing loss
sensorineural hearing
gjb2 gene mutations
enlarged vestibular aqueduct
gjb2 cx26 gene
proximal 6q deletions
abnormal ultrasound findings
chromosome 13 syndrome
retinal detachment
polycystic kidney
Resume
CV (Curriculum Vitae)
Education
- Studied human medicine at the Charles University in Prague
- Obtaining a license for medical practice
- Obtaining specialization in pediatrics
- Received additional qualifications in the field of medical genetics
- Postgraduate courses in medical genetics at the Institute of Postgraduate Medical Education in Prague
- Postgraduate courses in medical genetics at the European Scholl of Medical Genetics in Genoa
Experience
- Department of internal medicine at the Hospital in Susice
- 1987 Department of genetics at the University Hospital in Motola
- 2003 Department of genetics at the Gennet Clinic Letna Prague
Languages
English
Czech
Publications
The Cause of Hereditary Hearing Loss in GJB2 Heterozygotes-A Comprehensive Study of the GJB2/DFNB1 Region.
1 May, 2021
Spectrum and frequencies of non GJB2 gene mutations in Czech patients with early non-syndromic hearing loss detected by gene panel NGS and whole-exome sequencing.
December, 2020
Moderate sensorineural hearing loss is typical for DFNB16 caused by various types of mutations affecting the STRC gene.
December, 2019
Location
Kostelní, 292/9, 170 00 Prague, Czechia
FAQ
Where does the doctor practice?
What is the specialization of MUDr. Dagmar Raskova?
The primary specialization of the doctor is pediatrics and medical genetics.
What is the experience of the specialist?
MUDr. Dagmar Raskova has been practicing for more than 37 years.
MUDr. Dagmar Raskova
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