SE-ATLAS

Mapping of Health Care Providers
for People with Rare Diseases

Zentrum für pädiatrische Endokrinologie und Diabetologie am LMU Klinikum München

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Münchener Zentrum für seltene Erkrankungen (MZSE) am LMU Klinikum
Care for Rare Center am Dr. von Haunerschen Kinderspital am LMU Klinikum München

Description of facility

Director / Spokesperson
Prof. Dr. Heinrich Schmidt
Information
Care facility for children
Description
Das Zentrum für pädiatrische Endokrinologie und Diabetologie ist ein Referenzzentrum für seltene pädiatrische Erkrankungen. Kinder mit Wachstumsproblemen (Kleinwuchs, Großwuchs) können eine Hormonstörung haben und benötigen eine gezielte diagnostische Abklärung, bevor eine Behandlung möglich ist.
Hormonstörungen gehen unter anderem von der Hirnanhangsdrüse, der Schilddrüse, den Nebennieren (AGS, adrenogenitales Syndrom) und den Keimdrüsen aus. Diese Störungen können Wachstum, intellektuelle Entwicklung und Pubertät nachhaltig beeinflussen.
Die meisten dieser Störungen werden heute ambulant diagnostiziert und behandelt.

Care provisions

This facility offers the following
  • Diagnostic
  • Therapy

Contact

Terminvereinbarung Endokrinologische Sprechstunde
089 440053927
089 440053921
Simone.Kroke@med.uni-muenchen.de
Website https://www.lmu-klinikum.de/hauner/kinder-und-kinderpoliklinik/abteilungen/endokrinologie/21b1fd02ed584eda

Address

Lindwurmstraße 4
80337 München

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Languages

Germany.png Deutsch
United_Kingdom.png Englisch

Preview of the assigned diseases 6

Adrenogenital syndrome
Multiple endocrine neoplasia
Non-acquired panhypopituitarism
Noonan syndrome
Prader-Willi syndrome
Silver-Russell syndrome
Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1 Prader-Willi syndrome due to paternal 15q11q13 deletion Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2 Prader-Willi syndrome due to imprinting mutation Prader-Willi syndrome due to translocation Prader-Willi syndrome Familial medullary thyroid carcinoma MAGEL2-related Prader-Willi-like syndrome Congenital lipoid adrenal hyperplasia due to STAR deficency Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency Silver-Russell syndrome due to an imprinting defect of 11p15 Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency Silver-Russell syndrome due to 7p11.2p13 microduplication Silver-Russell syndrome due to 11p15 microduplication Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency Non-classic congenital lipoid adrenal hyperplasia due to STAR deficency Classic congenital lipoid adrenal hyperplasia due to STAR deficency Silver-Russell syndrome due to maternal uniparental disomy of chromosome 11 Noonan syndrome Generalized glucocorticoid resistance syndrome Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, simple virilizing form Multiple endocrine neoplasia type 1 Multiple endocrine neoplasia type 2 Multiple endocrine neoplasia Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, salt wasting form Multiple endocrine neoplasia type 4 Silver-Russell syndrome Non-acquired panhypopituitarism Rare hyperthyroidism Rare hypoparathyroidism Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15 Hyperandrogenism due to cortisone reductase deficiency Congenital adrenal hyperplasia Adrenogenital syndrome MIRAGE syndrome Multiple endocrine neoplasia type 2A Silver-Russell syndrome due to a point mutation Multiple endocrine neoplasia type 2B Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7
11.559205348.1302821Zentrum für pädiatrische Endokrinologie und Diabetologie am LMU Klinikum München
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Last updated: 31.01.2025