SE-ATLAS

Mapping of Health Care Providers
for People with Rare Diseases

Nuklearmedizin am Universitätsklinikum Marburg

Description of facility

Director / Spokesperson
Prof. Dr. med. Markus Luster
Information
Care facility for adults and children
Description
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

Address

Baldingerstraße
35043 Marburg

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Languages

Germany.png Deutsch
United_Kingdom.png 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