SE-ATLAS

Mapping of Health Care Providers
for People with Rare Diseases

Klinik für Endokrinologie und Stoffwechselerkrankungen am Universitätsklinikum Essen

Description of facility

Director / Spokesperson
Prof. Dr. Dr. med. D. Führer-Sakel
Information
Care facility for adults
Description
An der Klinik für Endokrinologie und Stoffwechselerkrankungen werden Patienten mit Erkrankungen der hormonproduzierenden Drüsen und Stoffwechselstörungen nach neuesten Diagnostik- und Therapiestandards betreut. Derartige Erkrankungen können vielfältige Ursachen haben und gehen oft mit Hormonüberschuß oder Hormonmangel, Neubildungen (Tumoren) oder Autoimmunerkrankungen einher. Durch die interdisziplinäre Vernetzung mit anderen Kliniken des Universitätsklinikums Essen bietet die Klinik mit fachübergreifenden Behandlungskonzepten eine optimale, patientenorientierte Betreuung.

Care provisions

This facility offers the following
  • Diagnostic
  • Therapy

Contact

Sekretariat
0201 7236401
Gabriele.Schreiber@uk-essen.de
Website http://uk-essen.de/endokrinologie/

Address

Hufelandstraße 55
45147 Essen

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Languages

Germany.png Deutsch
United_Kingdom.png Englisch

European Reference Network 1

Preview of the assigned diseases 5

Rare genetic thyroid disease Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome Apparent mineralocorticoid excess Primary hypergonadotropic hypogonadism-partial alopecia syndrome Hypogonadism-mitral valve prolapse-intellectual disability syndrome Rare endocrine disease Male hypergonadotropic hypogonadism-intellectual disability-skeletal anomalies syndrome Syndromic obesity Woodhouse-Sakati syndrome Familial hyperinsulinism Neuroendocrine neoplasm Proximal myotonic myopathy Turner syndrome Genetic non-syndromic obesity Rare diabetes mellitus Obesity due to congenital leptin deficiency Rare adrenal disease Rare dyslipidemia Polyendocrinopathy Rare thyroid disease Difference of sex development Autosomal recessive infantile hypercalcemia Primary adrenal insufficiency Pseudohypoparathyroidism Pituitary deficiency Familial multinodular goiter Chronic primary adrenal insufficiency Disorders of vitamin D metabolism Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome Deafness-hypogonadism syndrome Hyperinsulinism due to INSR deficiency Genetic obesity Rare parathyroid disease and phosphocalcic metabolism anomaly Neuroectodermal-endocrine syndrome Retinohepatoendocrinologic syndrome Neonatal diabetes mellitus Acrodysostosis with multiple hormone resistance Hypergonadotropic hypogonadism-cataract syndrome Rare precocious puberty Hypothalamic adipsic hypernatraemia syndrome Duplication of the pituitary gland Non-acquired premature ovarian failure Acquired premature ovarian failure Rare insulin-resistance syndrome Noonan syndrome Mikati-Najjar-Sahli syndrome Genetic lipodystrophy Rare diabetes mellitus type 1 Acquired lipodystrophy Congenital thyroid malformation without hypothyroidism Combined immunodeficiency due to LRBA deficiency Rare diabetes mellitus type 2 Familial hyperprolactinemia Rare thyroid tumor Oncogenic osteomalacia Congenital isolated hyperinsulinism Familial hyperaldosteronism Familial tumoral calcinosis Corticosteroid-binding globulin deficiency Adrenal/paraganglial tumor Pituitary adenoma Rare parathyroid tumor Rare hypothalamic or pituitary disease 46,XX difference of sex development Gastroenteropancreatic neuroendocrine neoplasm Obesity due to SIM1 deficiency Multiple polyglandular tumor Sex chromosome difference of sex development Moyamoya angiopathy-short stature-facial dysmorphism-hypergonadotropic hypogonadism syndrome Primary pigmented nodular adrenocortical disease Growth hormone insensitivity syndrome Rare endocrine growth disease Rare hypothyroidism Familial hypocalciuric hypercalcemia Severe early-onset obesity-insulin resistance syndrome due to SH2B1 deficiency Primary lipodystrophy Bangstad syndrome Rare hyperthyroidism Steinert myotonic dystrophy Hydrocephalus-obesity-hypogonadism syndrome Adrenocortical carcinoma Cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome Obesity due to congenital leptin resistance Non-insulinoma pancreatogenous hypoglycemia syndrome Rare hypoparathyroidism Hypocalcemic vitamin D-resistant rickets Autoimmune polyendocrinopathy Cushing syndrome Hypocalcemic vitamin D-dependent rickets Neonatal severe primary hyperparathyroidism Congenital adrenal hyperplasia Rare hyperparathyroidism Rare primary hyperaldosteronism ACTH-independent Cushing syndrome due to rare cortisol-producing adrenal tumor Non-acquired pituitary hormone deficiency Adrenogenital syndrome Familial hyperthyroidism due to mutations in TSH receptor Rare hypoaldosteronism Autosomal dominant hypocalcemia Rare hyperlipidemia 46,XY difference of sex development Hereditary pheochromocytoma-paraganglioma Rare hypolipidemia Acquired pituitary hormone deficiency Obesity due to CEP19 deficiency X-linked intellectual disability, Cilliers type Congenital hypothyroidism Diencephalic syndrome X-linked intellectual disability, Van Esch type Hypoinsulinemic hypoglycemia and body hemihypertrophy Rare syndromic dyslipidemia Autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome Craniopharyngioma Thymic neuroendocrine tumor Rare disorder with hypergonadotropic hypogonadism X-linked adrenoleukodystrophy X-linked acrogigantism

Provided care options 2

# Contact person
1
Spezialambulanz für Hormon- und Stoffwechselerkrankungen im Erwachsenenalter
Prof. Dr. Dr. med. D. Führer-Sakel

0201 7236303
Website
Sprechzeiten nach Vereinbarung.

2
Spezialambulanz für Tumorerkrankungen der endokrinen Organe (ENETS zertifiziert)
Prof. Dr. Dr. med. D. Führer-Sakel

0201 7236405
Website
Sprechzeiten nach Vereinbarung.

6.98877708984298951.43510405Klinik für Endokrinologie und Stoffwechselerkrankungen am Universitätsklinikum Essen
Last updated: 26.07.2023