CzMA JEP Home page CZECH MEDICAL ASSOCIATION J. Ev. PURKYNĚ
Journals - Article
CzMA JEP Home page News About Assocation Publishing Division Medical Journals Searching Supplements Catalogue
 
  Česky / Czech version Čs. Pediat., 57, 2002, No. 6, p. 296-298
 
Berardinelli-Seip Syndrome  
Seemanová E. 

Oddělení klinické genetiky Ústavu biologie a lékařské genetiky 2.LF UK,FN v Motole,Praha, vedoucí MUDr.M.Havlovicová
 


Summary:

       Berardinelli-Seip syndrome is an autosomal recessive syndrome due to a defect of insulin receptors.Deficient insulin binding to insulin receptors leads to insulin resistance with hyperinsulinism,hyperglycaemia and non-ke- tonaemic diabetes mellitus.The defect of lipid metabolism is manifested by lipodystrophy,premature ageing and hepatopathy.The clinical prognosis of the patient as well as the genetic prognosis of reproduction of his parents are unsatisfactory.Two genes responsible for this trait BSCL1 on 9q34 and BSCL2 on 11q13 were detected recently. There is genetic heterogeneity,the other genes were not yet mapped and therefore effective prevention is available only to some families at risk.

        Key words: Berardinelli-Seip syndrome,autosomal recessive inheritance,insulin resistance,mutation in genes BSCL1 on 9q34 and BSCL2 in region 11q13 or others,genetic heterogeneity
       

Order this issue

  BACK TO CONTENTS  
 
 
| HOME PAGE | CODE PAGE | CZECH VERSION |
©  1998 - 2008 CZECH MEDICAL ASSOCIATION J. E. PURKYNĚ
Created by: NT Servis, s.r.o., hosted by P.E.S. consulting, s.r.o.
WEBMASTER