SE-ATLAS

Mapping of Health Care Providers
for People with Rare Diseases

Zentrum für pädiatrische Endokrinologie und Diabetologie der Universitätsmedizin Frankfurt

Description of facility

Head of Institution
Dr. med. U. Paetow (Leiter); Prof. Dr. med. M. Kieslich (Stellvertreter)
Information
Care facility for children
Description
Hormone werden beim Menschen in vielen Organen gebildet und sind am Wachstum und der Entwicklung beteiligt. Erkrankungen des hormonellen Systems können durch die hormonbildenden Drüsen selbst oder durch andere Erkrankungen verursacht werden. Sie müssen rechtzeitig erkannt werden, damit Folgeschäden abgewendet werden können.

In der pädiatrischen Endokrinologie werden alle hormonellen Störungen bei Neugeborenen, Kindern und Jugendlichen behandelt.  Die Kinderendokrinologen arbeiten daher eng mit allen Teilgebieten der Kinderheilkunde und Jugendmedizin zusammen.

Die Schwerpunkte sind:
- Wachstumsstörungen (z.B. Kleinwuchs)
- Schilddrüsenerkrankungen (z.B. angeborene Hypothyreose)
- Störungen der Pubertätsentwicklung (z.B. vorzeitige Pubertätsentwicklung)
- Störungen der Geschlechtsentwicklung (z.B. chromosomale Auffälligkeiten)
- Nebennierenerkrankungen (z.B. Adrenogenitales Syndrom)
- Erkrankungen der Hirnanhangsdrüse (z.B. Hypophyseninsuffizienz)
- Störungen des Knochenstoffwechsels (z.B. Osteoporose)
- Störungen des Lipoprotein-Stoffwechsels (z.B. hohes Cholesterin)
- Seltene und syndromale Erkrankungen mit hormonellen Auffälligkeiten (z.B. Prader-Willi-Syndrom)

In der endokrinologischen Sprechstunde können Mädchen mit Turner-Syndrom untersucht, beraten und behandelt werden. In Zusammenarbeit mit der Erwachsenenendokrinolgie ist die pädiatrische Endokrinologie als Zentrum für die medizinische Versorgung von Mädchen und erwachsenen Frauen mit Turner-Syndrom zertifiziert.

Care provisions

This facility offers the following
  • Clinical studies / research
  • Diagnostic
  • Therapy
  • Contact with support groups
    Turner-Syndrom-Vereinigung Deutschland e.V.

Contact

Ambulanz
069 630180400
TerminanfrageKKJM@unimedizin-ffm.de
Website https://www.unimedizin-ffm.de/einrichtungen/kliniken/klinik-fuer-kinder-und-jugendmedizin/leistungsspektrum/neurologie-neurometabolik-und-praevention-mit-endokrinologie-und-diabetologie/ambulanz-fuer-neuropaediatrie-2

Address

Theodor Stern Kai 7
60590 Frankfurt am Main
Klinik für Kinder- und Jugendmedizin

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Languages

Germany.png Deutsch
United_Kingdom.png Englisch

Preview of the assigned diseases 1

Turner syndrome Prader-Willi syndrome Hypothyroidism due to deficient transcription factors involved in pituitary development or function Moebius syndrome-axonal neuropathy-hypogonadotropic hypogonadism syndrome Non-acquired pituitary hormone deficiency Combined pituitary hormone deficiencies, genetic forms Pituitary stalk interruption syndrome Congenital hypothyroidism due to maternal intake of antithyroid drugs Johanson-Blizzard syndrome Genetic transient congenital hypothyroidism Non-acquired combined pituitary hormone deficiency-sensorineural hearing loss-spine abnormalities syndrome Muscular pseudohypertrophy-hypothyroidism syndrome Hypothyroidism due to TSH receptor mutations Laron syndrome with immunodeficiency McCune-Albright syndrome Allan-Herndon-Dudley syndrome Obesity-colitis-hypothyroidism-cardiac hypertrophy-developmental delay syndrome Non-acquired panhypopituitarism Autoimmune polyendocrinopathy type 2 Isolated congenital hypogonadotropic hypogonadism Laurence-Moon syndrome Hypohidrotic ectodermal dysplasia-hypothyroidism-ciliary dyskinesia syndrome Aromatase deficiency Neonatal iodine exposure Pituitary resistance to thyroid hormone Transient congenital hypothyroidism due to neonatal factor Transient congenital hypothyroidism due to maternal factor Cataract-intellectual disability-hypogonadism syndrome Bardet-Biedl syndrome Congenital isolated ACTH deficiency Classic galactosemia Septopreoptic holoprosencephaly CHARGE syndrome Short stature due to primary acid-labile subunit deficiency Ataxia-hypogonadism-choroidal dystrophy syndrome Pallister-Hall syndrome Congenital adrenal hyperplasia Isolated follicle stimulating hormone deficiency Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency Congenital lipoid adrenal hyperplasia due to STAR deficency Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency Aromatase excess syndrome Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency Normosmic congenital hypogonadotropic hypogonadism Short stature due to partial GHR deficiency Short stature-delayed bone age due to thyroid hormone metabolism deficiency Congenital hypothyroidism Short stature due to GHSR deficiency Pendred syndrome Short stature-pituitary and cerebellar defects-small sella turcica syndrome Hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency Non-acquired combined pituitary hormone deficiency Familial adrenal hypoplasia with absent pituitary luteinizing hormone X-linked adrenal hypoplasia congenita Kallmann syndrome Athyreosis Semilobar holoprosencephaly Congenital hypothyroidism due to transplacental passage of TSH-binding inhibitory antibodies Primary congenital hypothyroidism without thyroid developmental anomaly Alobar holoprosencephaly Idiopathic congenital hypothyroidism Lobar holoprosencephaly X-linked central congenital hypothyroidism with late-onset testicular enlargement Isolated thyroid-stimulating hormone deficiency Growth delay due to insulin-like growth factor I resistance Growth delay due to insulin-like growth factor type 1 deficiency Rare endocrine growth disease Isolated thyrotropin-releasing hormone deficiency Septo-optic dysplasia spectrum Deficiency in anterior pituitary function-variable immunodeficiency syndrome Fetal iodine syndrome Non-acquired isolated growth hormone deficiency Laron syndrome Rare peripheral precocious puberty Autoimmune polyendocrinopathy type 1 Blepharophimosis-ptosis-epicanthus inversus syndrome Transient congenital hypothyroidism Woodhouse-Sakati syndrome Growth hormone insensitivity syndrome Familial peripheral male-limited precocious puberty Rare precocious puberty Congenital hypothyroidism due to developmental anomaly Thyroid ectopia Familial thyroid dyshormonogenesis Thyroid hemiagenesis Thyroid hypoplasia 46,XX gonadal dysgenesis Primary congenital hypothyroidism Permanent congenital hypothyroidism Central congenital hypothyroidism Resistance to thyrotropin-releasing hormone syndrome Congenital hypogonadotropic hypogonadism
8.6592596769332950.094113955199084Zentrum für pädiatrische Endokrinologie und Diabetologie der Universitätsmedizin Frankfurt
Last updated: 02.10.2026