se-atlas

Mapping of Health Care Providers
for People with Rare Diseases

Medizinische Klinik für Endokrinologie und Stoffwechselmedizin an der Charité Berlin

Decription of facility

Director / Spokesperson
Prof. Dr. med. Joachim Spranger
Information
Care facility for adults
Decription

Die Klinik für Endokrinologie und Stoffwechselmedizin (einschließlich Arbeitsbereich Lipidstoffwechsel) behandelt erwachsene Patienten aus dem gesamten Spektrum seltener endokrinologischer Erkrankungen. Dies sind u.a. Patienten mit hereditären oder seltenen Formen von Adipositas oder Bluthochdruck, Diabetes mellitus, Fettstoffwechselstörungen, Schilddrüsenerkrankungen, Störungen des Knochenstoffwechsels, Erkrankungen der Hirnanhangsdrüse oder der Nebennieren.
Die Standorte der Klinik mit ihren Ambulanzen, der Station und Tagesklinik sind verteilt auf die Campi Charité Mitte, Benjamin Franklin (Steglitz), Virchow-Klinikum (Wedding) sowie Berlin-Buch.

Consultation hours

Special consultation hours:
Mo - Do 8:00 - 16:00 Uhr sowie Fr 8:00 - 13:00 Uhr.

Care provisions

This facility offers the following
  • Participation in registries
    u.a. Deutsches Akromegalie-Register, Deutsches Cushing-Register
  • Genetic counselling
  • Clinical studies / research
    u.a. klinische Studien zu seltenen endokrinen Tumoren (ACC, Phäochromozytom etc)
  • Diagnostic
  • Therapy
  • Contact person for patients with an unclear diagnosis
    Abklärung gemeinsam mit dem Berliner Centrum für Seltene Erkrankungen (BCSE)

Contact

Sekretariat
030 450614264
030 450514950
ambulanz-endokrinologie@charite.de
Website

https://endokrinologie.charite.de/

Address

Charitéplatz 1
10117 Berlin

Campus Charité Mitte

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Languages

Germany.png Deutsch
United_Kingdom.png Englisch

Certificates 1

European Reference Network 2

Preview of the assigned diseases 15

Hartnup disease Mucopolysaccharidosis type 2 Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency Mucopolysaccharidosis type 4 Mucopolysaccharidosis type 6 Congenital disorder of glycosylation Lysinuric protein intolerance Niemann-Pick disease type C, juvenile neurologic onset Argininosuccinic aciduria Ornithine transcarbamylase deficiency Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib Glycogen storage disease due to glucose-6-phosphatase deficiency type Ia Fructose-1,6-bisphosphatase deficiency Carnitine palmitoyltransferase II deficiency Systemic primary carnitine deficiency Gaucher disease Multiple acyl-CoA dehydrogenase deficiency Very long chain acyl-CoA dehydrogenase deficiency Medium chain acyl-CoA dehydrogenase deficiency Disorder of fructose metabolism Niemann-Pick disease type B Niemann-Pick disease type A Beta-mannosidosis Neurometabolic disorder due to serine deficiency Alpha-mannosidosis Maple syrup urine disease Mucopolysaccharidosis type 1 Phenylketonuria Disorder of galactose metabolism Leigh syndrome Non-acquired pituitary hormone deficiency Acquired lipodystrophy Familial nonmedullary thyroid carcinoma VIPoma Genetic obesity Acquired pituitary hormone deficiency Overgrowth/obesity syndrome Familial medullary thyroid carcinoma Myopathy and diabetes mellitus MELAS MODY Cushing syndrome Cushing syndrome due to ectopic ACTH secretion Osteonecrosis ACTH-independent Cushing syndrome Medullary thyroid carcinoma ACTH-dependent Cushing syndrome Alkaptonuria Pseudohypoparathyroidism Apparent mineralocorticoid excess Rare diabetes mellitus Rare adrenal disease Pituitary deficiency Polyendocrinopathy Chronic primary adrenal insufficiency Acquired chronic primary adrenal insufficiency Rare genetic diabetes mellitus Hypocalcemic rickets Rare genetic thyroid disease Disorders of vitamin D metabolism X-linked hypophosphatemia Pituitary adenoma Pseudohypoparathyroidism type 1A Pseudopseudohypoparathyroidism Hypertension due to gain-of-function mutations in the mineralocorticoid receptor Pseudohypoparathyroidism type 1C Primary lipodystrophy Complete androgen insensitivity syndrome Pituitary carcinoma Triple A syndrome Pituitary resistance to thyroid hormone Glycogen storage disease due to acid maltase deficiency Neuroendocrine neoplasm Tumor of endocrine glands Familial hyperprolactinemia Dent disease Rare diabetes mellitus type 1 Rare insulin-resistance syndrome Pituitary apoplexy Von Hippel-Lindau disease Non-functioning paraganglioma Hypocalcemic vitamin D-dependent rickets Rare diabetes mellitus type 2 Peripheral resistance to thyroid hormones Other rare diabetes mellitus Pseudohypoparathyroidism type 1B Familial hyperaldosteronism type III Sporadic pheochromocytoma/secreting paraganglioma Pseudohypoparathyroidism type 2 Multiple endocrine neoplasia type 1 Multiple endocrine neoplasia type 2 Hyperandrogenism due to cortisone reductase deficiency Anaplastic thyroid carcinoma Hereditary pheochromocytoma-paraganglioma Congenital isolated hyperinsulinism Multiple endocrine neoplasia type 2A Differentiated thyroid carcinoma Addison disease Familial hyperaldosteronism type I Growth hormone insensitivity syndrome Familial hyperaldosteronism type II Sporadic pheochromocytoma Generalized resistance to thyroid hormone Familial hypocalciuric hypercalcemia Prolactinoma Sporadic secreting paraganglioma Multiple endocrine neoplasia type 2B Congenital adrenal hyperplasia Familial hyperaldosteronism Adrenogenital syndrome Partial androgen insensitivity syndrome Acute adrenal insufficiency Familial hyperreninemic hypoaldosteronism type 1 Pituitary tumor Familial hyperreninemic hypoaldosteronism type 2 HNF1B-related autosomal dominant tubulointerstitial kidney disease Familial hypocalciuric hypercalcemia type 2 Rare endocrine disease Familial hypocalciuric hypercalcemia type 3 Multiple endocrine neoplasia type 4 Familial hypocalciuric hypercalcemia type 1 Acromegaly Multiple endocrine neoplasia Idiopathic juvenile osteoporosis Catecholamine-producing tumor Insulin autoimmune syndrome Ectopic aldosterone-producing tumor Acquired premature ovarian failure Adrenocortical carcinoma Kallmann syndrome Non-acquired premature ovarian failure Maternally-inherited diabetes and deafness 46,XY disorder of sex development of endocrine origin Rare genetic bone disease Hypocalcemic vitamin D-resistant rickets Syndromic obesity Androgen insensitivity syndrome Thyroid tumor Insulin-resistance syndrome type A Thyroid carcinoma Insulin-resistance syndrome type B Cushing disease Localized lipodystrophy Pseudohypoaldosteronism type 2 Familial papillary or follicular thyroid carcinoma Insulinoma

Provided care options 6

# Contact person
1
Kompetenzzentrum für Seltene Stoffwechselkrankheiten
Athanasia Ziagaki

030 450553814
Email
Website
Telefonzeiten: Mo - Do 13:30 - 15:00 Uhr, Fr 12:30 - 14:00 Uhr, Sprechzeiten nach Vereinbarung

2
Spezialambulanz für angeborene oder erworbene Knochenerkrankungen
Dr. Lukas Maurer

030 450614264
Email
Website
Sprechzeiten nach Vereinbarung.

3
Spezialambulanz für endokrine Tumore
Knut Mai

030 450614264
Email
Website
Sprechzeiten nach Vereinbarung.

4
Spezialambulanz für seltene Diabetesformen
Thomas Bobbert

030 450614264
Email
Website
Sprechzeiten nach Vereinbarung.

5
Spezialambulanz für seltene Hypophysen-Erkrankungen
Christian Strasburger

030 450614264
Email
Website
Sprechzeiten nach Vereinbarung.

6
Spezialambulanz für seltene Nebennierenerkrankungen
Knut Mai

030 450614264
Email
Website
Sprechzeiten nach Vereinbarung.

13.37896585464477752.5244595525717Medizinische Klinik für Endokrinologie und Stoffwechselmedizin an der Charité Berlin
Last updated: 30.03.2021