SE-ATLAS

Mapping of Health Care Providers
for People with Rare Diseases

Medizinische Klinik für Endokrinologie und Stoffwechselmedizin an der Charité Berlin

Description of facility

Director / Spokesperson
Prof. Dr. med. Knut Mai
Information
Care facility for adults and children
Description
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

Telefonische Sprechzeiten: Telefonische Anfragen für Kinder: Do 14:00 - 16:00 Uhr. Telefonische Anfragen für Erwachsene: Di 10:00 - 11:00 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 with support groups
    Verein VHL (von Hippel - Lindau) betroffener Familien e.V.

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

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

Provided care options 6

# Contact person
1
Spezialambulanz für angeborene oder erworbene Knochenerkrankungen
Dr. Lukas Maurer

030 450514252
Email
Website
Sprechzeiten nach Vereinbarung.

2
Kompetenzzentrum für Seltene Stoffwechselkrankheiten
Dr. med. Athanasia Ziagaki

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

3
Spezialambulanz für seltene Hypophysen-Erkrankungen
Prof. Dr. med. Christian Strasburger

030 450514152
Email
Website
Sprechzeiten nach Vereinbarung.

4
Spezialambulanz für seltene Diabetesformen
PD Dr. med. Thomas Bobbert

030 450553252
Email
Website
Sprechzeiten nach Vereinbarung.

5
Spezialambulanz für seltene Nebennierenerkrankungen
Prof. Dr. med. Knut Mai

030 450514252
Email
Website
Sprechzeiten nach Vereinbarung.

6
Spezialambulanz für endokrine Tumore
Prof. Dr. med. Knut Mai

030 450514252
Email
Website
Sprechzeiten nach Vereinbarung.

13.37896585464477752.5244595525717Medizinische Klinik für Endokrinologie und Stoffwechselmedizin an der Charité Berlin
Last updated: 27.03.2024