pes cavus उदाहरण वाक्य
उदाहरण वाक्य
- Despite various presentations and descriptions of pes cavus, not all incarnations are characterised by an abnormally high medial longitudinal arch, gait disturbances, and resultant foot pathology.
- In the absence of neurological, congenital, or traumatic causes of pes cavus, the remaining cases are classified as being idiopathic because their aetiology is unknown.
- A combination of any or all of these elements can also be seen in a combined type of pes cavus that may be further categorized as flexible or rigid.
- Progressive muscle wasting results in weakness of peronei ), gait ataxia, pes cavus, postural tremors and static tremor of the upper limbs, kyphoscoliosis, and foot deformity.
- In pure "'pes cavus "', the calcaneus is neither dorsiflexed nor in varus and is highly arched due to a plantarflexed position of the forefoot on the rearfoot.
- Foot pain in people with pes cavus may result from abnormal plantar pressure loading because, structurally, the cavoid foot is regarded as being rigid and non-shock absorbent and having reduced ground contact area.
- Among the cases of neuromuscular pes cavus, 50 % have been attributed to Charcot-Marie-Tooth disease, which is the most common type of inherited neuropathy with an incidence of 1 per 2, 500 persons affected.
- Factors considered influential in the development of pes cavus include muscle weakness and imbalance in neuromuscular disease, residual effects of congenital clubfoot, post-traumatic bone malformation, contracture of the plantar fascia, and shortening of the Achilles tendon.
- "' Pes cavovarus "', the most common type of pes cavus, is seen primarily in neuromuscular disorders such as Charcot-Marie-Tooth disease and, in cases of unknown aetiology, is conventionally termed idiopathic.
- Loss-of-function " CUL4B " mutation events have been discovered in numerous patients with, which is characterized by aggressive outbursts, seizures, relative macrocephaly, central obesity, hypogonadism, pes cavus and tremor . " CUL4B " mutations have also been associated with malformations of cortical development.