SE-ATLAS

Mapping of Health Care Providers
for People with Rare Diseases

Klinik für Pädiatrische Nieren-, Leber- und Stoffwechselerkrankungen der Medizinischen Hochschule Hannover

Description of facility

Director / Spokesperson
Prof. Dr. med. Dieter Haffner
Information
Care facility for children
Description
Die Klinik für Pädiatrische Nieren-, Leber- und Stoffwechselerkrankungen behandelt Kinder und Jugendliche mit allen Krankheitsbildern aus den Bereichen pädiatrische Nephrologie, Endokrinologie, Gastroenterologie, Hepatologie, Neurologie und Stoffwechselerkrankungen. Ein besonderer Schwerpunkt liegt in der interdisziplinären Behandlung und Erforschung komplexer Erkrankungen und in der Nieren-/Lebertransplantation.
Die Klinik führt 30 Betten auf 2 Stationen. Stationär behandelt werden ca. 1.600 Patienten pro Jahr und 10.000 Patienten ambulant. Jährlich werden 20 Nieren- und 30 Lebertransplantationen vorgenommen. Ein interdisziplinäres Team mit 17 Fachärzten (Nephrologie, Hypertensiologie, Gastroenterologie/ Hepatologie, Neurologie, Endokrinologie und Stoffwechselerkrankungen) ist für die Behandlung verantwortlich. Die Klinik ist mit mehreren Einzelzentren am Zentrum für Seltene Erkrankungen der MHH beteiligt. Die pädiatrische Sonographie ist DEGUM zertifiziertes Ausbildungszentrum (Ausbilderin DEGUM Stufe III).

Care provisions

This facility offers the following
  • Clinical studies / research
  • Diagnostic
  • Therapy

Contact

Prof. Dr. med. Dieter Haffner
0511 5323213
0511 5323911
Website https://mhh-kinderklinik.de/

Address

Carl-Neuberg-Straße 1
30625 Hannover

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Languages

Germany.png Deutsch
United_Kingdom.png Englisch

European Reference Network 1

Mentioned by the following facilities 2

Preview of the assigned diseases 9

PrP systemic amyloidosis Immune dysregulation-inflammatory bowel disease-arthritis-recurrent infections syndrome Eosinophilic gastroenteritis Congenital enteropathy due to enteropeptidase deficiency Aplasia cutis congenita-intestinal lymphangiectasia syndrome Chronic diarrhea with villous atrophy Primary sclerosing cholangitis Primitive portal vein thrombosis Neonatal hemochromatosis Autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome Whipple disease Fanconi-Bickel syndrome Intractable diarrhea of infancy Syndromic diarrhea Mitochondrial DNA depletion syndrome, hepatocerebrorenal form Autosomal dominant polycystic kidney disease Autosomal recessive polycystic kidney disease Primary biliary cholangitis Rare gastroesophageal disease Rare vascular liver disease Alagille syndrome CADDS Rare pancreatic disease Rare metabolic liver disease Solitary rectal ulcer syndrome Rare parenchymal liver disease Acute infantile liver failure-multisystemic involvement syndrome Rare biliary tract disease Steroid dehydrogenase deficiency-dental anomalies syndrome Isolated polycystic liver disease Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 Hereditary fructose intolerance Intestinal lymphangiectasia Alpha-1-antitrypsin deficiency Tyrosinemia type 1 Congenital pancreatic cyst Familial hypercholanemia Pancreatic insufficiency-anemia-hyperostosis syndrome Crigler-Najjar syndrome Congenital sucrase-isomaltase deficiency Congenital intestinal transport defect Hyperbiliverdinemia Hepatic veno-occlusive disease Intestinal disease due to fat malabsorption Intestinal disease due to vitamin absorption anomaly Congenital enteropathy involving intestinal mucosa development Sandifer syndrome Congenital intestinal disease due to an enzymatic defect Galactosemia Short bowel syndrome Rare inflammatory bowel disease Rare hereditary hemochromatosis Peroxisome biogenesis disorder Follicular cholangitis and pancreatitis Wilson disease Congenital lactase deficiency Glycogen storage disease due to glucose-6-phosphatase deficiency Autoimmune hepatitis Recurrent acute pancreatitis Hepatoportal sclerosis Non-hypoproteinemic hypertrophic gastropathy Chronic intestinal failure Glycogen storage disease due to glycogen branching enzyme deficiency Zollinger-Ellison syndrome Glycogen storage disease due to liver glycogen phosphorylase deficiency Reynolds syndrome Dubin-Johnson syndrome Radiation proctitis Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins FTH1-related iron overload Severe immune-mediated enteropathy Neonatal inflammatory skin and bowel disease Low phospholipid-associated cholelithiasis Neonatal ichthyosis-sclerosing cholangitis syndrome Rotor syndrome Isolated biliary atresia Chronic diarrhea due to glucoamylase deficiency Idiopathic achalasia Glycogen storage disease due to liver phosphorylase kinase deficiency Trehalase deficiency Caroli disease Dietary iron overload disease Chronic hiccup Autoimmune enteropathy type 3 Autoimmune enteropathy type 2 Undetermined colitis Autoimmune pancreatitis Transient familial neonatal hyperbilirubinemia Hereditary chronic pancreatitis Congenital respiratory-biliary fistula Budd-Chiari syndrome Rare hepatic disease Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency Rare intestinal disease Biliary atresia with splenic malformation syndrome Eosinophilic esophagitis Familial intrahepatic cholestasis Malakoplakia Fulminant viral hepatitis Enteric anendocrinosis Hepatic veno-occlusive disease-immunodeficiency syndrome Plummer-Vinson syndrome Cystinosis Gastric linitis plastica

Provided care options 3

# Contact person
1
Sprechstunde für Kinder und Jugendliche mit Lebererkrankungen
Prof. Dr. med. Ulrich Baumann

0511 5323233
Email
Website
Sprechzeiten nach Vereinbarung.

2
Nephrologische Sprechstunde
Prof. Dr. Lars Pape

0511 530480
Email
Website
Sprechzeiten nach Vereinbarung. Die Sprechstunde wird in Kooperation mit dem KfH Nierenzentrum für Kinder und Jugendliche durchgeführt.

3
Zentrum für Kindergastroenterologie
Prof. Dr. med. Ulrich Baumann; Dr. med. Eva-Doreen Pfister

0511 5323233
Email
Website
Sprechzeiten nach Vereinbarung.

9.80713248252868852.382053500256596Klinik für Pädiatrische Nieren-, Leber- und Stoffwechselerkrankungen der Medizinischen Hochschule Hannover
Last updated: 20.12.2022