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At a group meeting in early 1993 to discuss the final draft of our paper on 22q11 deletion in DiGeorge syndrome, I pointed out that the variable clinical features associated with the deletion could be embraced in the acronym CATCH22.1 The idea was endorsed by the then editor of the Journal of Medical Genetics and the term became even more prominent when Judith Hall chose it as the title for the associated editorial.2I had presented it by then to the David Smith meeting to general acclaim and it was not until we used it at the UK Clinical Genetics Society that the criticism surfaced that the term carried a negative connotation. In his original book, Heller used the term to describe the challenge whereby insanity was a basis for discharge from air combat but to request discharge was proof of sanity.3 The term became more widely used in some countries to denote a “no win” situation. Another criticism of the term, which I recognised almost immediately after it reached print, was that the term “A” referring to “Abnormal facies” was a difficult aspect when counselling. My personal practice was to take CA to mean Cardiac Abnormality and put the “Anomalies of facial development” in parentheses. Subsequently, we qualified the term further and suggested that a more acceptable alternative would be the CATCH phenotype, omitting the “22” and with it the negative connotation.4
“CATCH phenotype” avoids use of the word “syndrome”. In theory this is a neutral term meaning “running together” but it can be taken to have a negative meaning. In particular, trisomy 21 is usually called Down’s syndrome in the English speaking world and, given the widespread recognition of the disorder, many people associate “syndrome” with learning disability. The original purpose of the CATCH acronym was to provide an alternative to the long running debate over eponyms. The name associated in most minds with the disorder was and is DiGeorge, yet the severe neonatal phenotype he first noted5 can result from other defects such as 10p13 and can be a phenocopy owing to maternal diabetes.6 ,7Historically, the Japanese work was contemporary and led to the careful delineation of conotruncal anomaly face syndrome which we showed subsequently to result from deletion of 22q11.8Strong9 provided the most complete description including dominant transmission, cardiac involvement in the form of right aortic arch, and late onset psychosis but the most compelling and widely used alternative name remains velocardiofacial syndrome or VCFS. The associated eponymous title has gained less favour because most people find Bob Shprintzen’s name hard to say and even harder to spell!
We suggested that one way of combining these various eponyms and acronyms would be to retain DiGeorge syndrome for the severe neonatal presentation, particularly where there is overt thymic hypoplasia and hypocalcaemia, while VCFS could be used for those children with a predominantly childhood presentation dominated by nasal speech owing to palatal insufficiency. The original work of Takao and his continued active leadership in international cardiovascular development research led us to suggest that Takao syndrome could be an alternative to conotruncal anomaly face (CTAF), where cardiovascular anomalies such as tetralogy of Fallot with major aorticopulmonary collaterals are the most prominent features. All these presentations could then be seen as differing clinical expressions of the CATCH phenotype.
Behind these explanations of why CATCH22 was invented there is, of course, the attraction of conceiving a memorable title, likened recently by Schrander-Stumpel10 to playing Scrabble. This is a fair criticism and if the patient groups object then the term CATCH22 cannot be used. We still have the difficulty that simply attaching the name 22q11 deletion fails to address the common spectrum of phenotypes and the rarer syndromic associations such as Opitz G/BBB11 and Cayler syndrome.12
This review is unlikely to change the preference of those who prefer to equate all 22q11 deletions with DiGeorge syndrome. Despite historical claims, Strong syndrome should not be used and conotruncal anomaly face syndrome would be better called Takao syndrome if it is to be retained at all. Velocardiofacial syndrome or VCFS is now well established and deserves continued widespread recognition as the best term for the typical child with characteristic facial appearance and palatal insufficiency. Many will continue to use 22q11 deletion syndrome as a satisfactory term13 and, given its high frequency,14 the consistency of the deleted region involved, and the fact that all the children have “the look” regardless of whether they have other features, this is a defensible position. For those with affection for the acronym, the embracing CATCH phenotype should now indicate Cardiac Abnormality, T cell deficit, Clefting, and Hypocalcaemia. Whatever term is used, we must always be sensitive to the need to avoid diminishing the person in our attempts to attach a diagnostic label of any sort.
As the new millennium approaches, it seems an appropriate time to inter CATCH22. What better title for this article than the title of Heller’s new book Closing time?15
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