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39 results
  1. ... Search term GeneReviews Advanced Search Help < Prev Next > LMNA -Related Dilated Cardiomyopathy Ray E Hershberger , MD and ... following the usual guidelines [ Yancy et al 2013 ]. LMNA -related DCM Treatment of symptomatic DCM, including heart ...
  2. ... CMD. Learn more about the gene associated with LMNA-related congenital muscular dystrophy LMNA Inheritance L-CMD is considered an autosomal dominant ... family. Other Names for This Condition L-CMD LMNA-related CMD MDCL Muscular dystrophy, congenital, LMNA-related ...
  3. ... Gilford progeria syndrome. More About This Health Condition LMNA-related congenital muscular dystrophy At least 15 mutations ...
  4. ... with identification of a heterozygous pathogenic variant in LMNA that results in production of the abnormal lamin ... features of HGPS and are heterozygous for another LMNA pathogenic variant in exon 11 or intron 11 ...
  5. ... list><related-gene-list ><related-gene ><gene-symbol >LMNA</gene-symbol><ghr-page >https://medlineplus.gov/genetics/gene/lmna</ghr-page></related-gene><related-gene ><gene-symbol > ...
  6. ... Mutations in several genes, including EMD , FHL1 , and LMNA , can cause Emery-Dreifuss muscular dystrophy. Mutations in ... linked type of the condition. Mutations in the LMNA gene cause both the autosomal dominant and autosomal ...
  7. ... causes (e.g., pathogenic variants in DES , FLNC , LMNA , and SCN5A ) may have prominent conduction system disease ... isolated DCM. Emery-Dreifuss muscular dystrophy EMD FHL1 LMNA XL AD AR Joint contractures Increased serum creatine ...
  8. ... topic><topic ><url >https://medlineplus.gov/genetics/condition/lmna-related-congenital-muscular-dystrophy</url><title >LMNA-related congenital muscular dystrophy</title><other_names ><other_ ...
  9. ... by mutations in different genes. Mutations in the LMNA gene cause MADA, and mutations in the ZMPSTE24 ... play a role in many cellular processes. The LMNA gene provides instructions for making two related proteins, ...
  10. ... see Arginine:glycine amidinotransferase deficiency L-CMD, see LMNA-related congenital muscular dystrophy L-xylulose reductase deficiency, ... CLCN2-related leukoencephalopathy LMD, see Langer mesomelic dysplasia LMNA-related CMD, see LMNA-related congenital muscular dystrophy ...
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