[Prenatal diagnosis and therapy of adrenogenital syndrome with 21-hydroxylase deficiency. Position of the Pediatric Endocrinology Study Group of the German Society of Pediatrics and the Section of Pediatric Endocrinology of the German Society of Endocrinology].

Subjects

Subjects :

Chorionic Villi Sampling
Female
Genetic Carrier Screening
Humans
Infant, Newborn
Pregnancy
Adrenal Hyperplasia, Congenital diagnosis
Adrenal Hyperplasia, Congenital drug therapy
Adrenal Hyperplasia, Congenital genetics
Dexamethasone therapeutic use
Genetic Counseling
Prenatal Diagnosis

Details

Language :

German

ISSN :

0026-9298

Volume :

140

Issue :

9

Database :

MEDLINE

Journal :

Monatsschrift Kinderheilkunde : Organ der Deutschen Gesellschaft fur Kinderheilkunde

Publication Type :

Academic Journal

Accession number :

1435819