| Timothy syndrome | |
|---|---|
| Specialty | Neurology  |
Timothy syndrome is a rareautosomal-dominant disorder characterized by physical malformations, as well asneurological and developmental defects, including heartQT-prolongation,heart arrhythmias, structural heart defects,syndactyly (webbing of fingers and toes), andautism spectrum disorders. Timothy syndrome represents one clinical manifestation of a range of disorders associated with mutations inCACNA1C,[1] the gene encoding thecalcium channel Cav1.2 α subunit.
The most striking sign of Timothy syndrome type 1 is the co-occurrence of both syndactyly (about 0.03% of births) andlong QT syndrome (1% per year) in a single patient. Other common symptoms include cardiacarrhythmia (94%), heart malformations (59%), andautism or an autism spectrum disorder (80% who survive long enough for evaluation). Facial dysmorphologies such as flattened noses also occur in about half of patients. Children with this disorder have small teeth, which is due to poorenamel coating, are prone todental cavities and often require removal. The average age of death due to complications of these symptoms is 2.5 years,[2][3][4] although there have been multiple reports of patients living in to their mid- or late-twenties.[5]
Timothy syndrome type 2 has largely the same symptoms as the classical form. Differences in the type 2 form are the lack of syndactyly, the presence of musculoskeletal problems (particularly hyperflexible joints), and often hip dysplasia. Patients with Timothy syndrome type 2 also have more facial deformities, including protruding foreheads and tongues.[6]
Children with Timothy syndrome tend to be born viacaesarean section due to fetal distress.[2][3]
There are two recognized types of Timothy syndrome, classical (type-1) and a second type (type-2). They are both caused by mutations inCACNA1C, the gene encoding thecalcium channel Cav1.2 α subunit. Timothy syndrome mutations inCACNA1C cause delayed channel closing, also known as voltage-dependent inactivation, thus increased cellularexcitability.[5]
Both types of Timothy syndromes are caused bymutations inCACNA1C. These mutations are in exon 8 (type 2) and exon 8a (classical form, type 1). Exons 8 and 8A are mutually exclusive exons. Exon 8a is highly expressed in the heart, brain, gastrointestinal system, lungs, immune system, and smooth muscle. Exon 8 is also expressed in these regions and its level is roughly five-fold higher than exon 8a expression.[5]
One mutation is found in patients with classical Timothy syndrome,G406R, located just past the sixth membrane-spanning segment of domain 1 (D1S6). The conservedglycine at this position seems to be vital for proper voltage-dependent inactivation, as the mutant is lacking in this respect.[4] Timothy syndrome type 2 mutations are similar, being the identicalG406R mutation in the other splice form. A second mutation resulting inG402S, located a fewamino acids upstream, was originally also given the name of type 2, but it is now recognized as a variant that causes non-syndromic LQT8. The effect of theG406R mutations on channel function is identical in the two forms of Timothy syndrome.[6] The lack of proper voltage-dependent inactivation in these mutants causes prolonged inward current anddepolarization duringcardiac action potentials. This leads tolong QT syndrome and resultantarrhythmia. Because exon 8 has greater expression in the heart versus exon 8a, patients with Timothy syndrome type 2 have worsened cardiac defects compared to those with the classical form.[5]
A pig model of the disease, carrying the same mutation as the one found in patients, allowed to identify that the calcium overload state leads the development of a substrate for functionalreentry characterised by slowing of cardiac impulse propagation.[7] Single cell studies identified thatCaMKII autophosphorylation reduced the peak sodium current, thus causing the slowing of conduction.[7]
Syndactyly and other deformities are typically observed and diagnosed at birth. Long QT syndrome sometimes presents itself as a complication due to surgery to correct syndactyly. Other times, children collapse spontaneously while playing. In all cases, it is confirmed withECG measurements. Sequencing of theCACNA1C gene further confirms the diagnosis.[5]
Surgery is typically used to correct structural heart defects and syndactyly.Propranolol or otherbeta-adrenergic blockers are often prescribed, as well as insertion of apacemaker to maintain proper heart rhythm. With the characterization of Timothy syndrome mutations indicating that they cause defects incalcium currents,calcium channel blockers may be effective as a therapeutic agent.[6]
The prognosis for patients diagnosed with Timothy syndrome is very poor. Of 17 children analyzed in one study, 10 died at an average age of 2.5 years. Of those that did survive, three were diagnosed with autism, one with an autism spectrum disorder, and the last had severe delays in language development.[4] One patient with theG402S mutation was largely normal with the exception of heart arrhythmia.[6] Likewise, the mother of two Timothy syndrome patients also carried the mutation, but lacked any obvious phenotype. In both of these cases, however, the lack of severity of the disorder was due tomosaicism.[6][4]
Some of the abnormalities observed in Timothy syndrome were described in the 1990s. However, it was linked with calcium channel abnormalities in 2004, and the disorder was thence named "Timothy syndrome" in honor of Katherine W. Timothy, who was among the first to identify a case and performed much of the phenotypic analysis that revealed other abnormalities.[4]
