MUDr. Gabriela Kreckova
pediatrics and medical genetics
pediatrics and medical genetics
Overview
Country, City
Czechia, Liberec
Health facility
Gennet Clinic Liberec
Medical unit
Department of genetics
About the doctor
Skills & Expertise
genetics
pediatrics
phenotype
genes
kidney
hearing
failure
hereditary
mutations
chromosome
thrombocytopenia
deletion
fli1
col2a1
col11a1
Resume
CV (Curriculum Vitae)
Education
- Studied human medicine
- Obtaining a license for medical practice
- Obtaining specialization in pediatrics
- Received additional qualifications in the field of medical genetics
Experience
- Department of genetics at the Gennet Clinic Liberec
Languages
English
Czech
Publications
A founder COL4A4 pathogenic variant resulting in autosomal recessive Alport syndrome accounts for most genetic kidney failure in Romani people.
8 February, 2023
Expanding the phenotype spectrum associated with pathogenic variants in the COL2A1 and COL11A1 genes.
September, 2020
Mutations in eight small DFNB genes are not a frequent cause of non-syndromic hereditary hearing loss in Czech patients.
July, 2016
Location
Liliová, 1, 460 01 Liberec, Czechia
FAQ
Where does the doctor practice?
MUDr. Gabriela Kreckova works at Gennet Clinic Liberec.
What is the specialization of MUDr. Gabriela Kreckova?
The primary specialization of the doctor is pediatrics and medical genetics.
What is the rating of the doctor?
MUDr. Gabriela Kreckova is rated as 9.80 by AiroMedical.
MUDr. Gabriela Kreckova
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