Nuklearmedizin am Universitätsklinikum Marburg
Description of facility
Director / Spokesperson
Prof. Dr. med. Markus LusterInformation
Care facility for adults and childrenDescription
Als ein integraler Bestandteil der Patientenversorgung wird Nuklearmedizin bei der Diagnose, dem Management der Behandlung und der Vorbeugung ernsterer Erkrankungen verwendet. Nuklearmedizinische Bildgebungsverfahren sind häufig in der Lage, Abnormitäten sehr früh im Erkrankungsverlauf zu diagnostizieren, lange bevor medizinische Probleme mit anderen diagnostischen Tests offensichtlich werden. Diese Frühentdeckung erlaubt, Erkrankungen früher zu behandeln zu einem Zeitpunkt, zu dem therapeutisch mehr ausgerichtet werden kann. Insgesamt werden in der Klinik ca. 12.000 in vivo Untersuchungen und ca. 370 Behandlungen mit Radionukliden pro Jahr durchgeführt. Weiterhin zeichnet sie sich durch innovative Forschungsarbeiten aus, wozu auch die Entwicklung und klinische Erstanwendung neuer Radiopharmaka gehört.
Care provisions
This facility offers the following
-
Clinical studies / research
- Diagnostic
- Therapy
Contact
Anmeldung
06421 5862813
06421 5867025
nukmed@med.uni-marburg.de
Website
https://www.ukgm.de/ugm_2/deu/umr_nuk/index.html
Languages
Deutsch Englisch
European Reference Network 1
Preview of the assigned diseases 2
Hypothyroidism due to deficient transcription factors involved in pituitary development or function
Peripheral hypothyroidism
Congenital hypothyroidism due to maternal intake of antithyroid drugs
Genetic transient congenital hypothyroidism
X-linked central congenital hypothyroidism with late-onset testicular enlargement
Hypothyroidism due to TSH receptor mutations
Isolated thyroid-stimulating hormone deficiency
Allan-Herndon-Dudley syndrome
Obesity-colitis-hypothyroidism-cardiac hypertrophy-developmental delay syndrome
Isolated thyrotropin-releasing hormone deficiency
Neonatal iodine exposure
Pituitary resistance to thyroid hormone
Transient congenital hypothyroidism due to neonatal factor
Transient congenital hypothyroidism due to maternal factor
Infantile multisystem neurologic-endocrine-pancreatic disease
Peripheral resistance to thyroid hormones
Autoimmune polyendocrinopathy type 3
Rare hyperthyroidism
Generalized resistance to thyroid hormone
Rare hypothyroidism
Short stature-delayed bone age due to thyroid hormone metabolism deficiency
Pendred syndrome
Bamforth-Lazarus syndrome
IgG4-related thyroid disease
Johanson-Blizzard syndrome
Muscular pseudohypertrophy-hypothyroidism syndrome
Hypohidrotic ectodermal dysplasia-hypothyroidism-ciliary dyskinesia syndrome
Fetal iodine syndrome
Transient congenital hypothyroidism
Polyendocrine-polyneuropathy syndrome
Familial hyperthyroidism due to mutations in TSH receptor
Congenital hypothyroidism
Rare adult hypothyroidism
Syndromic hypothyroidism
Congenital hypothyroidism due to developmental anomaly
Athyreosis
Thyroid ectopia
Congenital hypothyroidism due to transplacental passage of TSH-binding inhibitory antibodies
Primary congenital hypothyroidism without thyroid developmental anomaly
Idiopathic congenital hypothyroidism
Familial thyroid dyshormonogenesis
Thyroid hemiagenesis
Blepharophimosis-intellectual disability syndrome, SBBYS type
Thyroid hypoplasia
Familial gestational hyperthyroidism
Brain-lung-thyroid syndrome
Primary congenital hypothyroidism
Permanent congenital hypothyroidism
Central congenital hypothyroidism
Resistance to thyrotropin-releasing hormone syndrome
8.805678150.8165649Nuklearmedizin am Universitätsklinikum Marburg
Last updated:
23.05.2024