Orphanet: Diagnostik der famili�ren partiellen Lipodystrophie Typ 3 PPARG Gen
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Diagnosis of familial partial lipodystrophy type 3 (PPARG gene)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 02/12/2014
  • Gemeinschaftspraxis fr Humangenetik Dres. Bier, Krger und Reif
  • Gemeinschaftspraxis fr Humangenetik
  • Gutenbergstr. 5
  • 01307 DRESDEN
  • GERMANY
  • Director of laboratory : Dr Stefan KRUEGER
  • More information
  • Phone : 49 (0)351 44 66 340
  • Additional Phone : -
  • Fax : 49 (0)351 44 66 3415
  • Website
  • Contact
Last update: December 2014

Responsible of diagnostic test

Purpose(s)

Post-natal diagnosis

Technical procedure(s)

Molecular genetics
Sequence analysis: entire coding region
Sanger sequencing

List of diseases and genes

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

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.