Tag Archives: rare disease

Rare Disease talks at BSMB meeting in Norwich

BSMBJoint meeting with British Society for Developmental Biology

September 1 @ 1:00 pm – September 3 @ 12:15 pm.

See here.

Rare disease talks include:-

Mike Briggs (Newcastle)

“Refining disease mechanisms in genetic skeletal diseases”

Madeleine Durbeej (Lund)

“Laminin-deficient muscular dystrophy: pathogenesis and development of treatment”

Cay Kielty (Manchester)

“Fibrillin microfibrils: genotype-to-phenotype in the fibrillinopathies”

Rare Diseases eBook from Experts and Families

Rare diseases ebookRare Genomics Institute is a a nonprofit organisation that uses crowdsourced funding to help find cures for children with rare diseases.

They are offering a free e-book with inspiring family case studies, interviews from experts and information in a Parent’s Toolkit.

The book includes many interviews with genomics experts:

  • Dr. Ada Hamosh of Johns Hopkins shares her advice for parents of kids with rare diseases
  • Dr. Emil Kakkis develops drugs for rare diseases
  • Dr. Kary Mullis, Nobel Prize winner, shares advice for rare disease parents

Remarkable stories from families living with rare diseases:

  • Amylynne Volker’s son was the first child saved through DNA sequencing
  • Police officer, Mark Dant, raised over $3M for research that saved his son Ryan’s life
  • Retta Beery’s twins are alive due to her own exhaustive medical research and genomics

Available here.

Gene identification in rare skeletal diseases

An interesting historical breakdown of gene identification for rare skeletal diseases in the 25 years from 1988 to 2011.

GSD gene identification

What becomes apparent is that technology clearly drives the process of gene discovery and that there are ‘peaks in discovery’ that are closely aligned with ‘new’ technologies.

  • The availability of highly informative microsatelllite markers, which could even be assembled into panels for multiplexing (pioneered by Jim Weber in Marshfield Wisconsin), heralded the first increase in gene identification starting in the early to mid 1990’s.
  • This approach was massively enhanced with the publication of the Human Genome, which allowed a rapid transition from candidate region to candidate genes. For example, in our multiple epiphyseal dysplasia (MED) study of 2001 we went from a linked candidate region of 60cM to three candidate genes; TIMP3, SDC1 and MATN3 – we chose wisely  Chapman et al 01.
  • High throughput SNP analysis aided in the identification of numerous genes responsible for recessive skeletal diseases through homozygosity mapping.
  • Most recently arrays and next generation sequencing has completely revolutionised disease gene discovery in rare (skeletal) diseases.



A super example of gene discovery using exome sequencing comes from Andreas Zankl, Matt Brown and colleagues.

In summary, exome sequencing of both parents and the affected siblings in this family identified:-

  • 90% of targeted nucleotides had coverage of >four-fold
  • 79% of targeted nucleotides had coverage >ten-fold
  • ~15,000 SNPs identified following bioinformatic filtering!


  • >96% SNPs were reported in the recent dbSNP database and were therefore excluded from further analysis as unlikely to cause this rare disease.
  • Following the functional annotation of the remaining novel SNPs, focused analyses on a set of 483 unique novel coding non-synonymous SNPs that were detected in at least one sample.
  • Careful selection of ‘mode of inheritance’ allowed the identification of just four candidate genes.
  • In all but one gene the detected missense mutations were predicted to be tolerated in terms of effect upon protein function.

The single remaining candidate gene carried two novel alleles :-

  • One creating a premature stop codon.
  • One causing a missense mutation predicted to have a damaging effect on protein function.
  • POP1 a strong candidate for the disease-causing gene in this family.

Needless to say that this story made a great 2nd year undergraduate lecture Exome Lecture.