P.ser107leu in bicd2 is a mutation ‘hot neuro physiotherapy toronto spot’ causing distal spinal muscular atrophy brain oxford academic

We read with great interest the recent paper by rossor neuro physiotherapy toronto et al. (2015), reporting two new patients and summarizing observations on 30 previously neuro physiotherapy toronto published patients worldwide with BICD2-related spinal muscular atrophy. The work provides a timely overview of the main clinical neuro physiotherapy toronto characteristics observed in patients carrying the six currently known dominant neuro physiotherapy toronto BICD2 mutations. The paper also highlights the current knowledge of the structural neuro physiotherapy toronto and interaction specificities of BICD2 protein affected by the described neuro physiotherapy toronto missense mutations and supports dynein-dynactin trafficking impairment as a common pathomechanism ( oates et al., 2013).

The most common BICD2 mutation reported in four of the neuro physiotherapy toronto nine families was c.320CT, p.Ser107Leu. The mutation in two large pedigrees originating from australia and neuro physiotherapy toronto austria fell on a shared eight single nucleotide polymorphism (SNP) haplotype, spanning a 0.1 mb region and with a background frequency of 2% in the european population, suggesting a recent founder mutation between the two families. The same haplotype background was predicted in another affected family neuro physiotherapy toronto from the USA with european ancestors. A four-generation bulgarian family with turkish ethnic origin, originally reported by peeters et al. (2013), was the fourth family carrying the same mutation within a neuro physiotherapy toronto 12.7 mb region of linkage. In this family the disease arose as a consequence of neuro physiotherapy toronto a de novo mutation in the proband. In addition a three-generation dutch family published by neveling et al. (2013), had a similar phenotype and carried the same c.320CT, p.Ser107Leu missense mutation within a 10 mb region of linkage.

Here, we would like to expand the clinical presentation and haplotype neuro physiotherapy toronto background of the p.Ser107Leu BICD2 mutation with five additional patients from two north neuro physiotherapy toronto UK families ( fig. 1). A 41-year-old mother presented with her three children affected by the neuro physiotherapy toronto same disorder (family 1). She had a longstanding history of muscle weakness that has neuro physiotherapy toronto remained stable throughout her life. She was born with toe deformities and had mildly delayed neuro physiotherapy toronto motor development. She always had difficulties rising from the floor and with neuro physiotherapy toronto physical exercise. She developed a locked jaw in her university years and neuro physiotherapy toronto she was provided with a night splint to prevent its neuro physiotherapy toronto recurrence. On neurology examination she had mild weakness both proximally and neuro physiotherapy toronto distally in her lower limbs. She had a positive gower’s manoeuvre and she could not perform heel walking. Muscle strength in her upper limbs was entirely preserved but neuro physiotherapy toronto there was a mild scapular winging on the left side. Her deep tendon reflexes were brisk and asymmetric in her neuro physiotherapy toronto upper limbs. No cranial nerve involvement and sensory impairment were found. Except for a mildly elevated creatine kinase (292 U/l, normal 200), all other laboratory parameters were normal. Sensorimotor nerve conduction velocities and action potentials were within the neuro physiotherapy toronto normal ranges. On electromyography she had evidence of severe chronic neurogenic changes neuro physiotherapy toronto in both her upper and lower limbs. The findings were compatible with segmental motor neuronopathy. Her muscle MRI showed symmetrical prominent fatty replacement of gluteus neuro physiotherapy toronto medius, vastus lateralis, rectus femoris, semi-membranosus, lateral and medial gastrocnemius.

Pedigrees and clinical presentations of 2 new families carrying the neuro physiotherapy toronto p.Ser107Leu mutation in BICD2. ( A) pedigrees of the north UK families. Probands of each family are indicated by an arrow. ( B) image of the proband and her three affected children from neuro physiotherapy toronto family 1 presenting with lower limb wasting and feet deformities. ( C) images of proband from family 2 demonstrating wasting of lower neuro physiotherapy toronto extremities and his postsurgical feet position.

Her pregnancies and deliveries were uncomplicated. Her first born, currently 6-year-old daughter was noted to have a minor foot abnormality neuro physiotherapy toronto at birth. She did not walk until 20 months of age, and started walking on the medial aspect of her feet. The 5-year-old twin brothers had a very similar clinical course. Both had mild motor delay, and currently have mild weakness in both proximal and distal neuro physiotherapy toronto muscles of their lower limbs associated with disproportionate atrophy of neuro physiotherapy toronto the distal muscles ( fig. 1). Their upper body and arms are particularly strong with good neuro physiotherapy toronto manual dexterity but they show mild scapular winging. All three children have difficulties with rising from the floor, climbing stairs, running and they cannot perform heel walking. All receive physiotherapy and orthotic support. All four family members have normal cognition.

Another north british individual patient had no family history of neuro physiotherapy toronto neuromuscular disease (family 2). His parents were non-consanguineous and healthy, and his older brother is asymptomatic. The proband was born from an unremarkable pregnancy and delivery, but at birth he was noted with congenital bilateral talipes. After trials of physiotherapy and serial castings of his foot, the deformity was surgically corrected at age 1 year. His motor development was subsequently delayed, and he started walking only around the age of 3 neuro physiotherapy toronto years. He remained ambulant with a waddling gait, but he requires wheelchair support for longer distances. His cognition is normal.

On examination he had mild weakness, predominantly in the proximal muscles of his lower limbs accompanied neuro physiotherapy toronto by marked atrophy in the hip muscles. There was prominent muscle amyotrophy of both anterior and posterior neuro physiotherapy toronto compartments below the knee. He had full muscle power in the shoulders and upper neuro physiotherapy toronto limbs but he showed scapular winging bilaterally. Upper limb reflexes were easy to elicit while lower limb neuro physiotherapy toronto reflexes were reduced. He walked with a high-steppage gait and he could not achieve heel strike. Sensation was preserved. Nerve conduction studies were normal. Electromyography revealed fibrillation potentials and positive sharp waves and motor neuro physiotherapy toronto units were of markedly increased amplitude, polyphasic and unstable, suggesting chronic neurogenic process with spinal motor neuron involvement. Muscle biopsy showed neurogenic fibre atrophy but no other specific neuro physiotherapy toronto changes.

The clinical presentation of these five new patients is similar neuro physiotherapy toronto to the patients reported by rossor et al. (2015); however, we would emphasize that all our patients showed scapular winging, which we believe is a common feature of BICD2 deficiency. The heterozygous c.320CT, p.Ser107Leu mutation is the cause of the disease in both neuro physiotherapy toronto families. It followed an autosomal dominant inheritance pattern in family 1, however it is de novo in family 2, as both parents were tested negative. It is indicating that the c.320CT, p.Ser107Leu mutation arose independently in these two families. This mutation is located in a methylated cpg dinucleotide suggesting neuro physiotherapy toronto that recurrent mutations may occur at this position due to neuro physiotherapy toronto methylation-mediated deamination.

To determine whether the c.320CT, p.Ser107Leu mutation in family 1 is present on the same neuro physiotherapy toronto haplotype background as three of the families reported by rossor neuro physiotherapy toronto et al. (2015) or rather is a mutational hot spot, we performed haplotype analysis. HapMap (data release 28) SNP genotype data from the CEU population, in a region surrounding BICD2 were used to generate haplotypes neuro physiotherapy toronto in haploview ( www.Broadinstitute.Org). There were 10 different haplotypes present in the CEU european neuro physiotherapy toronto population in a single 0.1 mb block ( fig. 2). Genotypes from whole exome sequence data were present for the neuro physiotherapy toronto first five snps of the haplotypes and genotyping of a neuro physiotherapy toronto further seven haplotype tagging snps allowed us to show that neuro physiotherapy toronto the mutation was carried on a different haplotype background each neuro physiotherapy toronto of our two families. Additionally, the mutation-carrying haplotype in family 1 was present in 9.8% of the hapmap european population, which is presumably different from the haplotype reported by rossor neuro physiotherapy toronto et al. (2015), which was present in only 2% of europeans. Our haplotype analysis excludes the presence of a common founder neuro physiotherapy toronto mutation and further supports the theory that the c.320CT position is as a mutational hot spot.

Ten european haplotype blocks in a 0.1Mb region surrounding BICD2 from haplotype SNP ids 01 (rs556) to 89 (rs10117449). The BICD2 c.320CT mutation is located between snps 19 and 20. Haplotype snps 01, 04, 05, 07 and 08 were genotyped from whole exome sequence; snps 15, 19, 52, 63, 73, 88 and 89 were genotyped from sanger sequence (blue arrows). Affected members of family 1 shared haplotype block 3 (yellow box), present in the hapmap CEU population at a frequency of neuro physiotherapy toronto 0.098. The affected proband in family 2 had haplotype blocks 2 neuro physiotherapy toronto and 4 (red and blue boxes) in the region surrounding the mutation; recombination not observed in the CEU population occurred between snps neuro physiotherapy toronto 63 and 73, so that this proband also had part of either blocks neuro physiotherapy toronto 7, 8 or 10.

B.B. Is supported by the MRC centre for neuromuscular diseases. R.H. Is supported by the medical research council (UK) (G1000848) and the european research council (309548). P.F.C. Is a wellcome trust senior fellow in clinical science and neuro physiotherapy toronto an NIHR senior investigator who also receives funding from the neuro physiotherapy toronto medical research council (UK), the UK parkinson’s disease society, and the UK NIHR biomedical research centre for ageing and neuro physiotherapy toronto age-related disease award to the newcastle upon tyne foundation hospitals neuro physiotherapy toronto NHS trust. References

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