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PD. Dr. med. Ekkehart Lausch working place, University Hospital Freiburg
PD. Dr. med. Ekkehart Lausch
Excellent
AiroScore
9.80

PD. Dr. med. Ekkehart Lausch

pediatric genetic
pediatric genetic
User ScoreExperienceRatingPrice RangePublicationsOnline Consultations
96%31 years9.8/10$$$$80No

Overview

Country, City
Germany, Freiburg
Health facility
University Hospital Freiburg
Medical unit
Department of pediatric genetics

About the doctor

PD. Dr. med. Ekkehart Lausch is an experienced doctor with 30 years of experience in pediatric genetics. He obtained his medical license from the Johannes Gutenberg University. He completed his residency and postdoctoral research fellowship in emergency medicine and genetics at prestigious institutions like the University of Illinois and Rush University in Chicago. Dr. Lausch's career highlights include his specialization in pediatric genetics and his role as the head of the Department of Pediatric Genetics at the University Hospital Freiburg in Germany. He has published over 80 scientific papers on various genetic conditions and their treatment. His research has contributed to our understanding of diseases such as bone fragility, skeletal dysplasias, and congenital disorders of glycosylation. With his extensive expertise and dedication to pediatric genetics, Dr. Lausch is recognized as a leading authority in his practice area. His innovative research and commitment to high-quality care make him a valuable asset to the University Hospital Freiburg. Dr. Lausch's contributions to pediatric genetics have significantly advanced our understanding and treatment options for genetic conditions, making him an exceptional doctor.

Skills & Expertise

dysplasia
genetics
tumor
hepatitis
children
deficiency
mutation
gene
skeletal dysplasia
pediatrics
joint
chromosome
hyaline fibromatosis syndrome
fibromatosis
chondrodysplasia
beckwithwiedemann syndrome
thoracic dystrophy
wilms tumor
microdeletion
immunodeficiency
bone
neuropathy
hormone
dystrophy
spondyloepimetaphyseal dysplasia
isolated hypomethylation
genetic deficiency
cerebral calcifications
jeune syndrome
hypoplasia scapula
congenital chloride diarrhea
fam111a mutations
cousin syndrome
ciliary chondrodysplasia
hypomorphic mutations
congenital thrombocytopenia
pancytopenia immunodeficiency
xlinked megalocornea
vertebral changes
homozygous deletion
catelmanzkesyndromevcrl syndrome
congenital disorder
craniofacial dysmorphism
endochondral ossification
severe hypoglycemia
osteogenesis imperfecta
polycystic kidney
hormone deficiency
ellisvan creveld syndrome
hypoglycemia

Resume

CV (Curriculum Vitae)

Education
  • 1984-1993 Studied human medicine at the Johannes Gutenberg University in Mainz
  • Obtaining a license for medical practice
  • 1994-1996 Resident in emergency medicine at the University of Illinois and Rush University in Chicago
  • 1996 Defense of the dissertation in molecular oncology at the Department of genetics of the College of Medicine in Illinois
  • 1996-1997 Postdoctoral research fellowship at the Department of the genetics of the University of Illinois, College of Medicine in Chicago
  • 1997 Fellow in emergency medicine at the Rush Medical College in Chicago
  • 1999-2004 Resident in pediatrics at the Johannes Gutenberg University in Mainz
  • 2004 Obtaining specialization in pediatrics
  • 2004-2007 Clinical Fellow in pediatrics and residency in clinical genetics at the Johannes Gutenberg University in Mainz
  • 2009 Received additional qualifications in the field of human genetics
  • 2013 Habilitation and a teaching license at the University of Freiburg
Experience
  • 1997-1998 Research Assistant Professor of the Department of Genetics, College of Medicine, University of Illinois
  • 2008 Attending Physician, Department of pediatrics at the University Hospital Freiburg
  • 2013 Head of the Department of pediatric genetic at the University Hospital Freiburg

Languages

English flag
English
German flag
German

Publications

Acanthocytosis: a key feature for the diagnosis of abetalipoproteinemia.

29 June, 2023

Novel GNE Gene Variants Associated with Severe Congenital Thrombocytopenia and Platelet Sialylation Defect.

July, 2022

Uncovering pathways regulating chondrogenic differentiation of CHH fibroblasts.

12 December, 2021

Location

Hugstetter Str., 55, 79106 Freiburg, Germany

FAQ

Where does the doctor practice?

What is the specialization of PD. Dr. med. Ekkehart Lausch?

The primary specialization of the doctor is pediatric genetic.

What is the experience of the specialist?

PD. Dr. med. Ekkehart Lausch has been practicing for more than 31 years.

What is the rating of the doctor?

What topics does PD. Dr. med. Ekkehart Lausch expert at?

The doctor has excellent knowledge in dysplasia, genetics, tumor, hepatitis, children.

Is the specialist involved in the research?

Does the specialist offer online consultations?

No, PD. Dr. med. Ekkehart Lausch doesn’t perform virtual appointments.

PD. Dr. med. Ekkehart Lausch
PD. Dr. med. Ekkehart Lausch

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