Orphanet: Diagnostik des familiären Hypoaldosteronismus Typ 1 CYP11B1 und CYP11B2 Gen
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Diagnosis of familial hyperaldosteronism type 1 (CYP11B1, CYP11B2 genes)

  • Kinderendokrinologisches Labor - Universitres MVZ Kiel
  • Hormonzentrum fr Kinder und Jugendliche
  • Universittsklinikum Schleswig-Holstein - Campus Kiel
  • Arnold-Heller-Str. 3
  • 24105 KIEL
  • GERMANY
  • Director of laboratory : Pr Paul-Martin HOLTERHUS
  • More information
  • Phone : 49 (0)431 500 20271
  • Additional Phone : -
  • Fax : 49 (0)431 500 20274
  • Website
  • Contact
Last update: February 2018

Responsible of diagnostic test

Purpose(s)

Post-natal diagnosis

Technical procedure(s)

Molecular genetics
Sequence analysis: entire coding region
Sanger sequencing
Sequence analysis: entire coding region
NGS sequencing (except WES)

List of diseases and genes

List of diseases tested (1)
List of genes tested (including panels) (2)

Additional information

The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.