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