Studies of prevalence suggest that they are more common in patients with late-onset GSD II than in general population (16, 17). Some of the reported patients had neurological signs and/or symptoms directly related to cerebrovascular abnormalities, such as transient ischemic attacks and neurovascular conflicts resulting in cranial nerve involvement (16, 17). Rarely vascular abnormalities #selleck compound randurls[1|1|,|CHEM1|]# were described in different areas than the brain, such as aneurysms of the left ventricle

of the heart (18). Vacuolar degeneration and glycogen deposits were found in the vessel walls and in smooth muscle cells of cerebral arteries and other blood vessels (15). The progressive Inhibitors,research,lifescience,medical loss of integrity of these structures over the course of disease may explain the occurrence of dilatative

arteriopathies or aneurysms in these patients (16). There is a recent report of a late-onset GSD II patient with an intramuscular hemangioma located in the right semimembranosus muscle (19). Intramuscular hemangiomas are quite rare abnormalities and make up 0.8% of all hemangiomas (19). Although a coincidental Inhibitors,research,lifescience,medical occurrence can be not completely ruled out, the rarity of muscle hemangiomas in the general Inhibitors,research,lifescience,medical population as well as the propensity of GSDII patients to have vascular abnormalities should induce to evaluate also the peripheral vascular axes in the diagnostic process and follow-up of these subjects. Bone involvement A high frequency Inhibitors,research,lifescience,medical of vertebral and femur fractures was reported in infants and osteopenia was described in long-term survivors with infantile GSD II (2, 20-22). At present, not many studies on bone metabolism in late-onset GSD II are available (2). However, there is no doubt that bone involvement is an under-recognized issue in this group of patients. Bone mineral density is significantly lower in GSD II patients than in healthy individuals and osteoporosis is

present in both Inhibitors,research,lifescience,medical wheelchair-bound and ambulant patients (2, 23, unpublished personal observation). Oktenli described an adult patient who presented with low bone density and vertebral fragility associated with hypocalcaemia, hypocalciuria and renal magnesium wasting due to the accumulation of glycogen in distal tubules (24). Even though loss of muscle function and limited movement can contribute to loss of mineral content, development of osteopenia and a higher risk of fracture (2, 23, 24), further studies are mandatory in order to Oxalosuccinic acid explore the role of possible primary bone metabolism dysfunctions in the pathogenesis of bone alterations in this group of patients. Other features Fatigue is a frequent complaint of GSD II patients, it is characterized by difficulty in initiating and sustaining voluntary effort and is not related to age, sex or disease duration (25). The Fatigue Severity Scale (FSS) was assessed in an international population of 225 adults with GSDII and the mean FSS score was significantly higher than that of healthy controls (25).