Homozygous mutation in HSPB1 causing distal vacuolar myopathy and motor neuropathy

Case report. A 57-year-old woman, born to parents of Gujarati Indian descent (figure, A), presented at age 19 with pain and stiffness in her calves and a tendency to trip. In her 20s, a formal neurologic examination demonstrated predominantly distal lower limb weakness and normal upper limb muscle strength. Motor and sensory nerve conduction studies were normal with the exception that no motor response was elicited from the extensor digitorum brevis. Fibrillations and polyphasic action potentials were present on EMG. The creatine kinase (CK) level was 1,452 IU/L. A quadriceps muscle biopsy was performed at age 27 from which images were available in the records. At that time, muscle fiber diameters were large ranging from 50 to 80 mm. Many of the fibers contained single or multiple unrimmed vacuoles that appeared empty in the modified Gomori trichrome preparation (figure, B.a). There was no increase in endomysial connective tissue or evidence of inflammation, necrosis, or regeneration. There was no evidence of glycogen, increased lipid, or acid phosphatase staining in the vacuoles (figure, B.b). The ATPase at pH 9.5 demonstrated that most of the vacuolated fibers were of type 2, and electron microscopy showed electron-dense material within vacuoles (figure, B.c and d). The overall appearances were those of a vacuolar myopathy without any features suggesting neurogenic change, and she was diagnosed with a distal myopathy. She re-presented at age 57 following the development of slowly progressive severe upper and lower limb weaknesses. On examination at age 57, there was evidence of distal more than proximal upper limb weakness affecting wrist extension (Medical Research Council [MRC] grade 41/5), finger extension (4 1 5), first dorsal interossei (1/5), abductor pollicis brevis (3/5 right and 4/5 left), and abductor digiti minimi (3/5 right and 4/5 left). In the lower limbs, she had severe proximal weakness (grade 2/3) with no movement at the ankles. Sensory modalities were preserved except for reduced vibration sense at the ankles. She was areflexic. Her CK level was 404 IU/L. Neurophysiologic studies suggested an axonal motor neuropathy. Sensory nerve action potentials were, nevertheless, at the lower limit of normal for amplitude in the lower limbs (right sural 6 mV, right superficial peroneal 7 mV, and normal range .5 mV), and distal lower limb motor responses were absent. Needle EMG showed prominent chronic neurogenic changes with large motor units recruiting in reduced numbers but at increased firing rates to a reduced interference pattern. This EMG pattern was most pronounced distally but evident proximally in the upper and lower limbs. No low amplitude or brief polyphasic motor units were seen on any occasion at re-presentation. Muscle MRI was performed, showing widespread severe muscle fatty replacement (figure, C). There was no relevant family history. Her mother has diabetes and her father a right above knee amputation for peripheral vascular disease. Neither had neurologic complaints. However, clinical examination of both in their 80s revealed mild distal weakness (MRC grade 4/5) in the upper and lower limbs with areflexia. Pinprick sensation was reduced to the midforearm and foot in her mother. Her father had reduced vibration sense to the left ankle. Neurophysiologic testing was not possible in either. Targeted exome sequencing of the proband’s DNA using the Agilent Focused Exome kit identified a homozygous variant (c.418C.G, p.Arg140Gly) in HSPB1, which was confirmed by Sanger sequencing. Both parents were heterozygous. We have reported this variant previously in heterozygous form in individuals from 5 Indian Gujarati families with distal motor neuropathy.