Hyperinsulinism due to INSR deficiency
All Entries 4
Zentrum für Congenitalen Hyperinsulinismus (COACH) am Universitätsklinikum Magdeburg
Medizinische Fakultät Universitätsklinikum Magdeburg A.ö.R. Mitteldeutsches Kompetenznetz Seltene Erkrankungen - Magdeburg, Dessau, Halle (MKSE)
Leipziger Str. 44
39120 Magdeburg
0391 6724024
0391 67290038
Website
Email
Zentrum für Seltene Hormonelle Erkrankungen (ZSHE) am Universitätsklinikum Tübingen
Universitätsklinikum Tübingen Behandlungs- und Forschungszentrum für Seltene Erkrankungen (ZSE) Tübingen
Hoppe-Seyler-Str. 1
72076 Tübingen
07071 2983795
07071 294157
Website
Email
07071 2983670
07071 292784
Website
Email
Zentrum für Seltene Endokrine Erkrankungen (hormonelle Erkrankungen) am Universitätsklinikum Ulm
Universitätsklinikum Ulm Zentrum für Seltene Erkrankungen Universitätsmedizin Ulm
Eythstraße 24
89075 Ulm
0731 50057401
0731 50057407
Website
Email
- Rare diabetes mellitus
- Genetic obesity
- Craniopharyngioma
- Congenital hypogonadotropic hypogonadism
- Prolactinoma
- Acquired lipodystrophy
- Central diabetes insipidus
- Congenital isolated hyperinsulinism
- Multiple endocrine neoplasia
- Pseudohypoparathyroidism type 1A
- Addison disease
- Primary lipodystrophy
- Acromegaly
Kongenitaler Hyperinsulinismus e.V.
Rigaer Straße 87
10247
Berlin
- Autosomal dominant hyperinsulinism due to Kir6.2 deficiency
- Autosomal recessive hyperinsulinism due to SUR1 deficiency
- Diazoxide-sensitive diffuse hyperinsulinism
- Diazoxide-resistant hyperinsulinism
- Congenital isolated hyperinsulinism
- Hyperinsulinism due to UCP2 deficiency
- Diazoxide-resistant diffuse hyperinsulinism
- Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency
- Congenital hyperinsulinism due to HNF4A deficiency
- Hyperinsulinism due to INSR deficiency
- Diazoxide-resistant focal hyperinsulinism
- Autosomal dominant hyperinsulinism due to SUR1 deficiency
- Diazoxide-resistant focal hyperinsulinism due to Kir6.2 deficiency
- Autosomal recessive hyperinsulinism due to Kir6.2 deficiency
- Hyperinsulinism-hyperammonemia syndrome
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Care facilities 3
Zentrum für Congenitalen Hyperinsulinismus (COACH) am Universitätsklinikum Magdeburg
Medizinische Fakultät Universitätsklinikum Magdeburg A.ö.R. Mitteldeutsches Kompetenznetz Seltene Erkrankungen - Magdeburg, Dessau, Halle (MKSE)
Leipziger Str. 44
39120 Magdeburg
0391 6724024
0391 67290038
Website
Email
Zentrum für Seltene Hormonelle Erkrankungen (ZSHE) am Universitätsklinikum Tübingen
Universitätsklinikum Tübingen Behandlungs- und Forschungszentrum für Seltene Erkrankungen (ZSE) Tübingen
Hoppe-Seyler-Str. 1
72076 Tübingen
07071 2983795
07071 294157
Website
Email
07071 2983670
07071 292784
Website
Email
Zentrum für Seltene Endokrine Erkrankungen (hormonelle Erkrankungen) am Universitätsklinikum Ulm
Universitätsklinikum Ulm Zentrum für Seltene Erkrankungen Universitätsmedizin Ulm
Eythstraße 24
89075 Ulm
0731 50057401
0731 50057407
Website
Email
- Rare diabetes mellitus
- Genetic obesity
- Craniopharyngioma
- Congenital hypogonadotropic hypogonadism
- Prolactinoma
- Acquired lipodystrophy
- Central diabetes insipidus
- Congenital isolated hyperinsulinism
- Multiple endocrine neoplasia
- Pseudohypoparathyroidism type 1A
- Addison disease
- Primary lipodystrophy
- Acromegaly
Supportgroups 1
Kongenitaler Hyperinsulinismus e.V.
Rigaer Straße 87
10247
Berlin
- Autosomal dominant hyperinsulinism due to Kir6.2 deficiency
- Autosomal recessive hyperinsulinism due to SUR1 deficiency
- Diazoxide-sensitive diffuse hyperinsulinism
- Diazoxide-resistant hyperinsulinism
- Congenital isolated hyperinsulinism
- Hyperinsulinism due to UCP2 deficiency
- Diazoxide-resistant diffuse hyperinsulinism
- Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency
- Congenital hyperinsulinism due to HNF4A deficiency
- Hyperinsulinism due to INSR deficiency
- Diazoxide-resistant focal hyperinsulinism
- Autosomal dominant hyperinsulinism due to SUR1 deficiency
- Diazoxide-resistant focal hyperinsulinism due to Kir6.2 deficiency
- Autosomal recessive hyperinsulinism due to Kir6.2 deficiency
- Hyperinsulinism-hyperammonemia syndrome