SE-ATLAS

Mapping of Health Care Providers
for People with Rare Diseases

Hormonzentrum für Kinder und Jugendliche am Universitätsklinikum Schleswig-Holstein, Campus Kiel

Description of facility

Director / Spokesperson
Prof. Dr. med. Paul-Martin Holterhus
Information
Care facility for children
Description
Seit über 30 Jahren ist die Kinderendokrinologie, d.h., die Behandlung von Kindern und Jugendlichen mit Erkrankungen des Hormonsystems, ein Schwerpunkt der Kinderklinik des UK S-H am Campus Kiel. Dieser Schwerpunkt umfasst auch die Versorgung von Patienten mit Diabetes, eine der häufigsten Hormonstörungen des Kindes- und Jugendalters. Das Kieler Hormonzentrum für Kinder und Jugendliche ist zugleich Teil des „Hormonzentrums Nord“. Im „Hormonzentrum Nord“ sind alle Bereiche des Universitätsklinikums Schleswig-Holstein, die sich mit Hormonstörungen befassen, vernetzt. Um ihre Patienten und deren Familien umfassend versorgen zu können, arbeitet die Hormonsprechstunde der Kieler Kinderklinik mit einem breit aufgestellten Team. Dazu zählen spezialisierte Kinderärztinnen und Kinderärzte (Kinderendokrinologen und Diabetologen), Kinderkrankenschwestern, Arzthelferinnen, Diabetesberaterinnen, eine Ernährungsberaterin, Psychologen, Sozialarbeiterinnen, eine Chemikerin und Technische Assistentinnen im Kinderhormonlabor u.v.m.

Care provisions

This facility offers the following
  • Diagnostic
  • Therapy

Contact

Sekretariat
0431 50019017
0431 50020124
B.Mohr@uksh.de
Website http://www.uksh.de/kinderhormonzentrum-kiel

Address

Arnold-Heller-Straße 3
24105 Kiel
Haus C

Calculate route

Languages

Germany.png Deutsch
United_Kingdom.png Englisch

European Reference Network 1

Preview of the assigned diseases 1

Tetragametic chimerism X-linked lissencephaly with abnormal genitalia 46,XX difference of sex development induced by fetoplacental androgens excess 46,XY ovotesticular difference of sex development Penile agenesis Chondrodysplasia-difference of sex development syndrome 46,XY difference of sex development due to impaired androgen production Turner syndrome 46,XY difference of sex development of endocrine origin Monosomy X 46,XY difference of sex development due to 17-beta-hydroxysteroid dehydrogenase 3 deficiency 46,XY difference of sex development due to 5-alpha-reductase 2 deficiency Mosaic monosomy X Androgen insensitivity syndrome Difference of sex development Leydig cell hypoplasia 46,XX difference of sex development induced by exogenous maternal-derived androgen Frasier syndrome WAGR syndrome 46,XX difference of sex development induced by fetal androgens excess SERKAL syndrome 46,XX difference of sex development induced by endogenous maternal-derived androgen 46,XY difference of sex development due to a testosterone synthesis defect Denys-Drash syndrome Müllerian aplasia and hyperandrogenism Syndrome with 46,XX difference of sex development 46,XY difference of sex development due to a cholesterol synthesis defect 46,XY difference of sex development due to testicular steroidogenesis defect 46,XY difference of sex development due to adrenal and testicular steroidogenesis defect Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency Classic congenital lipoid adrenal hyperplasia due to STAR deficency Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency Aromatase deficiency Congenital lipoid adrenal hyperplasia due to STAR deficency Familial adrenal hypoplasia with absent pituitary luteinizing hormone 46,XX ovotesticular difference of sex development Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency 46,XY disorder of gonadal development 46,XY difference of sex development due to isolated 17,20-lyase deficiency Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency Meacham syndrome Partial androgen insensitivity syndrome Dysmorphism-short stature-deafness-difference of sex development syndrome Testicular agenesis Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, salt wasting form Non-classic congenital lipoid adrenal hyperplasia due to STAR deficency Generalized glucocorticoid resistance syndrome 46,XY complete gonadal dysgenesis 46,XX gonadal dysgenesis 49,XXXXY syndrome 48,XXXY syndrome 46,XX difference of sex development-anorectal anomalies syndrome Leydig cell hypoplasia due to partial LH resistance 46,XX difference of sex development-skeletal anomalies syndrome Leydig cell hypoplasia due to complete LH resistance 46,XY difference of sex development induced by maternal exposure to endocrine disruptors 46,XY difference of sex development-adrenal insufficiency due to CYP11A1 deficiency Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, simple virilizing form 46,XX difference of sex development Difference of sex development-intellectual disability syndrome 46,XX testicular difference of sex development Turner syndrome due to structural X chromosome anomalies Sex chromosome difference of sex development 46,XY gonadal dysgenesis-motor and sensory neuropathy syndrome Perrault syndrome Persistent Müllerian duct syndrome XY type gonadal dysgenesis-associated anomalies syndrome Complete androgen insensitivity syndrome 45,X/46,XY mixed gonadal dysgenesis Smith-Lemli-Opitz syndrome Palmoplantar keratoderma-XX sex reversal-predisposition to squamous cell carcinoma syndrome Campomelic dysplasia Distal deletion 9p 46,XY partial gonadal dysgenesis Lung fibrosis-immunodeficiency-46,XX gonadal dysgenesis syndrome 48,XXYY syndrome 46,XX difference of sex development induced by androgens excess Leydig cell hypoplasia due to LHB deficiency Sudden infant death-dysgenesis of the testes syndrome 46,XY difference of sex development due to a defect in testosterone metabolism by peripheral tissue 46,XY difference of sex development Syndrome with 46,XY difference of sex development Testicular regression syndrome Alpha-thalassemia-X-linked intellectual disability syndrome 46,XX disorder of gonadal development PAGOD syndrome 46,XX difference of sex development induced by maternal-derived androgen

Provided care options 1

# Contact person
1
Interdisziplinäre Sprechstunde bei Störungen der Geschlechtsentwicklung
Prof. Dr. med. Paul-Martin Holterhus

0431 50020160
Email
Website
Sprechzeiten nach telefonischer Vereinbarung.

10.14288732743867554.3304953Hormonzentrum für Kinder und Jugendliche am Universitätsklinikum Schleswig-Holstein, Campus Kiel
Last updated: 19.10.2022