To highlight Rare Disease Day this past February 28th, we’re featuring some personal stories from parents whose children live with rare conditions.

Today, our friend Steph Nimmo, from the “Was This in the Plan?” blog tells us about her gorgeous daughter Daisy, who has an extreme form of Costello syndrome.

When my daughter, Daisy, was born two months premature in December 2004, the chance she might have a rare disease did not cross my mind.

I knew that following antenatal testing she did not have Downs syndrome or a known gene mutation, so I just assumed that the problems she was experiencing post-birth were down to her early arrival. That was, until her consultant neonatologist called me in and asked my permission to call in a geneticist.

We were given a clinical diagnosis of Costello syndrome and this was confirmed a few months later, when a research breakthrough identified a mutation on a gene called H-Ras as being responsible, a mutation which our daughter was found to have.

Daisy is one of around just 250 in the world with Costello Syndrome. The mutation is on an oncogene, a cancer causing gene, which means that she has a 15 percent, increased risk of developing malignant tumors. Knowing this means that we are able to screen her regularly for tumours and be vigilant in watching for any suspicious changes.

The syndrome also affects growth, bones, the heart, development, vision and the gastrointestinal system. We contacted the Costello Syndrome support group and gained great comfort in meeting other families whose children who had similar features to Daisy, it was good to no longer feel so alone with this rare and scary life-limiting syndrome.

Daisy with other children with Costello Syndrome.

However when Daisy started developing problems which had not been documented  in the Costello Syndrome literature before, we were, to put it mildly, perplexed.  Daisy did not grow out of the feeding issues (or at least become stable with them) as the literature suggests. In fact she now has intestinal failure, she also developed neuropathic bladder and the icing on the cake has been the onset of uncontrolled, multi-focal epilepsy.

Time after time we would post updates on the support group listserv hoping that another family might shine some light on what was happening with Daisy and we might be able to gain some reassurance that she was not so different from the Costello syndrome norm.

The genetics team thinks that Daisy has an extreme manifestation of Costello Syndrome, a manifestation which may have appeared before in other children but thanks to excellent healthcare and early diagnosis she has survived the odds where others did not. Our blood has been taken for exome testing, to see if there is some other genetic reason for the severity of Daisy’s symptoms.

But whatever they find, it is what it is, we cannot change things, but hopefully we, and the geneticists can learn from it. A syndrome is ultimately a collection of symptoms on a continuum of severity and when it comes to Costello syndrome it seems that Daisy is the rarest of the rare.

Since the mapping of the human genome, the field of genetics has gone into warp drive. Not only has the gene which causes Costello Syndrome been identified, but a whole group of gene mutations on the same gene pathway called Ras-MAPK have been identified, mutations which, like the hras mutation which causes Costello Syndrome, are responsible for other syndromes with similar phenotypes.

In 2009 the term “Rasopathy” was coined to group together these syndromes which comprise Costello Syndrome, Noonan Syndrome, Cardiofaciocutanenous Syndrome,  Noonan Syndrome with multiple Lentigines (formerly LEOPARD syndrome), Neurofibromatosis Type 1, and other rare conditions all caused by a mutation of a gene along this common gene pathway.

There are numerous overlapping phenotypic features among the syndromes, including characteristic facial features, cardiac defects, cutaneous abnormalities, neurocognitive delay and a predisposition to malignancies. (Dr. Kate Rauen UCSF June 28, 2009).

Over the past few years there has been greater collaboration within the research community to look at Rasopathies as a whole and their overlaps in order to identify treatments to manage the impacts of these conditions. The bonus for our family of this wider collaboration is that we now have found that some of the symptoms Daisy exhibits which are not common in Costello Syndrome are well known in other syndromes among the rasopathies.

For example, epilepsy is well documented in Cardiofaciocutaneous syndrome and there are children with Noonan Syndrome who require intravenous nutrition (TPN) in the same way that Daisy does.


There are multiple benefits of collaboration between rare disease groups (such as the rasopathies). In the field of genetic research, more and more is being revealed on how the mutations on this pathway impact not only the individual syndromes but diseases as a whole– The Ras/MAPK pathway is essential in the regulation of the cell cycle, differentiation, growth and cell senescence, all of which are critical to normal development.

From the point of view of one family with a little girl with the rarest of the rare syndromes in the rasopathy group it means that we no longer feel so isolated and alone. Support groups are sharing information, joint conferences, research papers and symposiums. In the States, there are even rasopathy clinics with doctors who are experts in this group of syndromes and a unified website for us all to gather together wherever we are in the world.

Now not only does Daisy have her Costello family with whom she shares so many traits, but she has an extended family of ras-cousins, some of whom share some of her symptoms and suddenly for our family rare does no longer means alone.

If you want to learn more about the RASopathies, please go to