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Dr. med. Axel Bohring working place, University Hospital Munster
Dr. med. Axel Bohring
Excellent
AiroScore
9.90

Dr. med. Axel Bohring

human genetics, pediatrics
human genetics, pediatrics
User ScoreRatingPrice RangePublicationsOnline Consultations
97%9.9/10$$$$30No

Overview

Country, City
Germany, Munster
Health facility
University Hospital Munster
Medical unit
Department of human genetics

About the doctor

Dr. med. Axel Bohring is a highly skilled doctor specializing in human genetics and pediatrics. He has an extensive academic background, having studied human medicine and obtaining a license for medical practice. With his additional specialization in human genetics and pediatrics, Dr. Bohring brings a unique and comprehensive understanding to his expertise. Currently, Dr. Bohring serves as the Acting Director of the Institute at the Westphalian Wilhelms University in Munster, Germany. He is also affiliated with the Department of Human Genetics at the University Hospital Munster. Dr. Bohring's years of experience and expertise in the field led him to publish over 30 scientific publications. His research focuses on various genetic disorders, including frontometaphyseal dysplasia, CHARGE syndrome, and Bohring-Opitz syndrome. Through his research, Dr. Bohring aims to expand the understanding of these conditions and improve patient diagnosis and treatment options. Dr. med. Axel Bohring's dedication to his field and wealth of knowledge and experience make him a highly regarded doctor in human genetics and pediatrics. His contributions to scientific literature demonstrate his commitment to advancing research and improving patient care in genetics.

Skills & Expertise

genetics
dysplasia
frontometaphyseal dysplasia
phenotype
bohringopitz syndrome
charge syndrome
ehlersdanlos syndrome
hypohidrotic ectodermal dysplasia
trigonocephaly syndrome
truncating mutations
multiple osteochondromas
vertebral column
skeletal dysplasia
polytopic anomalies
prepubertal periodontitis
nodular heterotopia
meckelgruber syndrome
capillary dysplasia
pulmonary veins
tumorigenesis mutations
schwannomatosis
alveolar capillary dysplasia
lower vertebral column
sclerosing skeletal dysplasia
sporadic familial cases
misaligned pulmonary veins
kbg syndrome
osteochondromas
immunoglobulin
pancreas
mutation
face
anomalies
deletion
sclerosing
heterozygotes
agenesis
predispose
sweating
ectodermal dysplasia
dystrophies
haplotype
periventricular
heterotopia
pregnancy loss
genetic disorders
neurofibromatosis
retinal dystrophies
waardenburg syndrome
noonan syndrome

Resume

CV (Curriculum Vitae)

Education
  • Studied human medicine
  • Obtaining a license for medical practice
  • Obtaining specialization in pediatrics
  • Received additional specialization in human genetics
Experience
  • Acting director of the institute at the Westphalian Wilhelms University in Munster
  • Department of human genetics at the University Hospital Munster

Languages

English flag
English
German flag
German

Publications

ANKRD11 variants: KBG syndrome and beyond.

August, 2021

Prepubertal Periodontitis in a Patient with Combined Classical and Periodontal Ehlers-Danlos Syndrome.

24 January, 2021

Expanding the clinical spectrum of recessive truncating mutations of KLHL7 to a Bohring-Opitz-like phenotype.

December, 2017

Location

Albert-Schweitzer-Campus, 1, 48149 Munster, Germany

FAQ

Where does the doctor practice?

What is the specialization of Dr. med. Axel Bohring?

The primary specialization of the doctor is human genetics, pediatrics.

What is the rating of the doctor?

Dr. med. Axel Bohring is rated as 9.90 by AiroMedical.

What topics does Dr. med. Axel Bohring expert at?

The doctor has excellent knowledge in genetics, dysplasia, frontometaphyseal dysplasia, phenotype, bohringopitz syndrome.

Is the specialist involved in the research?

Does the specialist offer online consultations?

No, Dr. med. Axel Bohring doesn’t perform virtual appointments.

Dr. med. Axel Bohring
Dr. med. Axel Bohring

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