SE-ATLAS

Mapping of Health Care Providers
for People with Rare Diseases

Zentrum für seltene pädiatrische Nierenerkrankungen (ZSNeph) am Universitätsklinikum Tübingen

Description of facility

Director / Spokesperson
PD Dr. med. Marcus Weitz
Information
Care facility for children
Description
Das Zentrum für seltene pädiatrische Nierenerkrankungen (ZSNeph) ist eines der integrierten Fachzentren des Zentrums für Seltene Erkrankungen am Universitätsklinikum Tübingen. Es ist spezialisiert auf die Diagnostik, Erforschung und Behandlung von angeborenen und erworbenen seltenen Erkrankungen der Nieren und ableitenden Harnwege im Kindes- und Jugendalter. Die Betreuung der Patient:innen erfolgt in Kooperation mit dem KfH-Nierenzentrum für Kinder und Jugendliche und umfasst das gesamte diagnostische und therapeutische Spektrum der Kindernephrologie. Durch eine enge Zusammenarbeit mit nationalen und internationalen Expert:innen anderer Zentren für seltene Erkrankungen wird die Qualität einer kompetenten und innovativen Behandlung der Patient:innen sichergestellt. Die Beteiligung an nationalen und internationalen Studien mit speziellen nephrologischen Erkrankungen soll helfen, die Diagnostik und Therapie in unserem Fachgebiet zu verbessern. Bei der ganzheitlichen Betreuung der Patient:innen mit seltenen Nieren- und Harntrakterkrankungen verfolgt das Zentrum einen multidisziplinären Ansatz unter Einbezug vieler verschiedener Fachdisziplinen, um den betroffenen Kinder und Jugendlichen differenzierte und bestmögliche Behandlungsoptionen und ihren Familien eine umfassende psychosoziale Unterstützung anbieten zu können.

Consultation hours

Montag - Mittwoch: 08:00 - 13.00 Uhr und 14.30 - 15.30 Uhr; Donnerstag: 08:00 - 12.30 Uhr

Care provisions

This facility offers the following
  • Participation in registries
  • Social / legal advice
  • Genetic counselling
  • Clinical studies / research
  • Diagnostic
  • Therapy

Contact

Susanne Wernet, Andrea Thomas
07071 9425606
07071 94256111
kinderdialyse@med.uni-tuebingen.de
Website https://www.medizin.uni-tuebingen.de/de/das-klinikum/einrichtungen/kliniken/kinderklinik/kinderheilkunde-i/nephrologie

Address

Hoppe-Seyler-Straße 1
72076 Tübingen

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Languages

Germany.png Deutsch
United_Kingdom.png Englisch
Greece.png Griechisch
Turkey.png Türkisch

Preview of the assigned diseases 6

HANAC syndrome Autosomal recessive infantile hypercalcemia Bartter syndrome type 5 Liddle syndrome Renal-hepatic-pancreatic dysplasia Enamel-renal syndrome Autosomal dominant proximal renal tubular acidosis Cryoglobulinemic vasculitis Megacystis-megaureter syndrome Proximal renal tubular acidosis Alport syndrome Systemic lupus erythematosus Muckle-Wells syndrome Lipoprotein glomerulopathy Primary megaureter, adult-onset form Nail-patella syndrome Congenital primary megaureter, obstructed form Congenital primary megaureter, refluxing form Familial vesicoureteral reflux Renal agenesis Congenital primary megaureter, nonrefluxing and unobstructed form Atypical hemolytic uremic syndrome Action myoclonus-renal failure syndrome Primary membranoproliferative glomerulonephritis Alström syndrome Genetic steroid-resistant nephrotic syndrome Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome Renal tubular dysgenesis of genetic origin Dominant hypophosphatemia with nephrolithiasis or osteoporosis Pierson syndrome Congenital and infantile nephrotic syndrome Primary membranous glomerulonephritis Interstitial lung disease-nephrotic syndrome-epidermolysis bullosa syndrome Collagen type III glomerulopathy Dense deposit disease Distal renal tubular acidosis with anemia Leigh syndrome with nephrotic syndrome Denys-Drash syndrome Severe oculo-renal-cerebellar syndrome Fibronectin glomerulopathy Immunoglobulin-mediated membranoproliferative glomerulonephritis Congenital nephrotic syndrome, Finnish type X-linked Alport syndrome C3 glomerulonephritis Idiopathic steroid-sensitive nephrotic syndrome with secondary steroid resistance Frasier syndrome Idiopathic steroid-resistant nephrotic syndrome Idiopathic multidrug-resistant nephrotic syndrome Idiopathic steroid-resistant nephrotic syndrome with sensitivity to second-line immunosuppressive therapy Familial steroid-resistant nephrotic syndrome with adrenal insufficiency MYH9-related disease Nephrotic syndrome-epidermolysis bullosa-sensorineural deafness syndrome Idiopathic steroid-sensitive nephrotic syndrome Congenital membranous nephropathy due to fetomaternal anti-neutral endopeptidase alloimmunization Schimke immuno-osseous dysplasia Familial steroid-resistant nephrotic syndrome with sensorineural deafness Hereditary hypophosphatemic rickets with hypercalciuria Immunotactoid or fibrillary glomerulopathy Hypocomplementemic urticarial vasculitis Galloway-Mowat syndrome Autosomal dominant intermediate Charcot-Marie-Tooth disease type E Renal hypoplasia, unilateral Unilateral multicystic dysplastic kidney Oculocerebrorenal syndrome of Lowe Renal hypoplasia, bilateral De novo thrombotic microangiopathy after kidney transplantation Acquired monoclonal Ig light chain-associated Fanconi syndrome Distal renal tubular acidosis Autosomal recessive Alport syndrome Autosomal dominant Alport syndrome Bilateral multicystic dysplastic kidney Renal tubular dysgenesis due to twin-twin transfusion Juvenile polymyositis Atypical hemolytic uremic syndrome with anti-factor H antibodies Congenital thrombotic thrombocytopenic purpura Late-onset nephronophthisis Infantile nephronophthisis Primary hyperoxaluria type 2 Primary hyperoxaluria type 3 Xanthinuria type II Autosomal recessive proximal renal tubular acidosis Autosomal dominant distal renal tubular acidosis Cystinuria type B Cystinuria type A Hereditary amyloidosis with primary renal involvement Familial renal glucosuria Juvenile dermatomyositis Hemolytic uremic syndrome Atypical hemolytic uremic syndrome with complement gene abnormality Autosomal dominant hypophosphatemic rickets X-linked hypophosphatemia Renal pseudohypoaldosteronism type 1 Hypotonia-cystinuria syndrome Shiga toxin-associated hemolytic uremic syndrome Atresia of urethra Behçet disease CREST syndrome Cystinuria Apparent mineralocorticoid excess Anti-glomerular basement membrane disease Familial hyperaldosteronism type I Primary hyperoxaluria Autosomal recessive distal renal tubular acidosis LCAT deficiency Autosomal dominant polycystic kidney disease Williams syndrome Autosomal dominant tubulointerstitial kidney disease Familial hyperaldosteronism type III Methylmalonic acidemia with homocystinuria, type cblC Renal coloboma syndrome Autoimmune interstitial lung disease-arthritis syndrome Senior-Boichis syndrome Idiopathic hypercalciuria Primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement Isolated autosomal dominant hypomagnesemia, Glaudemans type EAST syndrome MUC1-related autosomal dominant tubulointerstitial kidney disease IgG4-related kidney disease Prune belly syndrome Renal dysplasia HNF1B-related autosomal dominant tubulointerstitial kidney disease Primary hypomagnesemia-refractory seizures-intellectual disability syndrome Renal dysplasia, unilateral Drug-related renal tubular dysgenesis Phosphoribosylpyrophosphate synthetase superactivity Takayasu arteritis Genetic primary hypomagnesemia with hypocalciuria Genetic primary hypomagnesemia with normocalciuria Pediatric systemic lupus erythematosus ALys amyloidosis AFib amyloidosis Nephronophthisis Systemic sclerosis Genetic primary hypomagnesemia Bartter syndrome Osteopetrosis with renal tubular acidosis Hemolytic uremic syndrome with DGKE deficiency Primary hypomagnesemia with secondary hypocalcemia AApoAII amyloidosis Eosinophilic granulomatosis with polyangiitis Anterior urethral valve Brachydactyly-arterial hypertension syndrome AH amyloidosis Dermatomyositis Microscopic polyangiitis Oligomeganephronia Nephrogenic diabetes insipidus Idiopathic non-lupus full-house nephropathy Relapsing polychondritis Autosomal recessive polycystic kidney disease Polymyositis Pseudohypoaldosteronism type 1 REN-related autosomal dominant tubulointerstitial kidney disease Familial primary hypomagnesemia with normocalciuria and normocalcemia Autosomal dominant primary hypomagnesemia with hypocalciuria Oncogenic osteomalacia Renal agenesis, bilateral Renal agenesis, unilateral Isolated epispadias Infection-related hemolytic uremic syndrome Bladder exstrophy Generalized pseudohypoaldosteronism type 1 Pauci-immune glomerulonephritis with ANCA Hereditary renal hypouricemia Joubert syndrome with oculorenal defect Exstrophy-epispadias complex Pseudohypoaldosteronism type 2 Immunoglobulin A vasculitis Polyarteritis nodosa Medullary sponge kidney Reynolds syndrome Pauci-immune glomerulonephritis without ANCA Sarcoidosis Autosomal recessive hypophosphatemic rickets Familial Mediterranean fever Joubert syndrome with renal defect Mixed connective tissue disease Light and heavy chain deposition disease Tubulointerstitial nephritis and uveitis syndrome Heavy chain deposition disease Light chain deposition disease Thrombotic thrombocytopenic purpura Non-amyloid monoclonal immunoglobulin deposition disease Multicystic dysplastic kidney Primary hypomagnesemia with hypercalciuria and nephrocalcinosis with severe ocular involvement AApoAI amyloidosis Dent disease Galactosemia Hereditary xanthinuria Von Hippel-Lindau disease Immune-mediated thrombotic thrombocytopenic purpura Juvenile nephronophthisis Gitelman syndrome Posterior urethral valve Giant cell arteritis Familial hyperaldosteronism type II Hypoxanthine-guanine phosphoribosyltransferase deficiency Primary hyperoxaluria type 1 Xanthinuria type I Buerger disease Pauci-immune glomerulonephritis Nephrogenic syndrome of inappropriate antidiuresis Granulomatosis with polyangiitis AApoAIV amyloidosis Dent disease type 2 Hypophosphatemic rickets Dent disease type 1 Congenital primary megaureter AL amyloidosis Familial hyperaldosteronism AA amyloidosis Hypohidrosis-electrolyte imbalance-lacrimal gland dysfunction-ichthyosis-xerostomia syndrome Streptococcus pneumoniae-associated hemolytic uremic syndrome Mitochondrial oxidative phosphorylation disorder Cloacal exstrophy Renal tubular dysgenesis Renal dysplasia, bilateral Adenine phosphoribosyltransferase deficiency Diffuse cutaneous systemic sclerosis Fetal lower urinary tract obstruction Primary Fanconi renotubular syndrome Arthrogryposis-renal dysfunction-cholestasis syndrome Immunotactoid glomerulopathy Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis Non-amyloid fibrillary glomerulopathy UMOD-related autosomal dominant tubulointerstitial kidney disease Renal hypoplasia Congenital renal artery stenosis Primary systemic amyloidosis Primary localized amyloidosis

Provided care options 6

# Contact person
1
Sprechstunde für genetisch bedingte Erkrankungen der Nieren und ableitenden Harnwege
PD Dr. med. Marcus Weitz

07071 9425606
Email
Sprechzeiten nach Vereinbarung.

2
Durchführung von Aphereseverfahren inkl. Leukapherese/-depletion, Immunadsorption, Plasmapherese, Lipidapherese und extrakorporaler Photopherese
PD Dr. med. Marcus Weitz

07071 9425606
Email
Sprechzeiten nach Vereinbarung.

3
Sprechstunde für Hämodialysepatienten
PD Dr. med. Marcus Weitz

07071 9425606
Email
Sprechzeiten nach Vereinbarung.

4
Sprechstunde für Peritonealdialysepatienten
PD Dr. med. Marcus Weitz

07071 9425606
Email
Sprechzeiten nach Vereinbarung.

5
Sprechstunde für nierentransplantierte Kinder und Jugendliche
PD Dr. med. Marcus Weitz

07071 9425606
Email
Sprechzeiten nach Vereinbarung.

6
Sprechstunde für angeborene und erworbene Erkrankungen mit Nieren- bzw. Harntraktbeteiligung
PD Dr. med. Marcus Weitz

07071 9425606
Email
Sprechzeiten nach Vereinbarung.

9.03898537158966248.53086926692498Zentrum für seltene pädiatrische Nierenerkrankungen (ZSNeph) am Universitätsklinikum Tübingen
Last updated: 26.04.2023