Progressive muscular dystrophy is a group Kamagra Soft SX”>Tadalis SX of genetic factors of muscle Buy Buy Brand Levitra Online baclofen online degenerative diseases.
Reflected mainly in the slow onset, gradual progress in muscle weakness and atrophy. According to the different distribution of affected muscle can be divided into several types:
1, Duchenne muscular dystrophy: for X-linked recessive genetic male disease, women carrying buy Kamagra Gold generic prescription abnormal genes, but not incidence. The incidence was particularly prevalent in children, and gradually progress. Start to behave as unstable Buy Accutane Online Pharmacy No Prescription Needed Jelly”>Cialis Jelly walking, easy-wrestling, housing difficulties, the future development of difficult to walk, before the age of 12 should not walk, can only stay in bed. Physical examination can be found in the limbs, especially limb-girdle Cialis muscular atrophy and weakness, who showed the typical wing-like shoulder, excessive lumbar lordosis when standing up, walking to both sides of the pelvis was duck swinging step; from the supine position starting immediately, they must first stand up for the prone position, then with both hands supporting the lower limbs gradually straighten Buy Viagra, Buy Cialis, Buy Levitra Without Prescription the body. Muscle showed some pseudo-hypertrophy, mostly gastrocnemius (calf), has also manifested in the deltoid muscle, genioglossus and so on, the appearance of pseudo-hypertrophy of the muscle developed a solid touch than normal muscle, but the decline in muscle strength. Facial and hand muscle atrophy can also be mild. Has often accompanied by cardiac involvement and mental retardation.
2, Becker muscular dystrophy: also known as benign muscular dystrophy, but Brand Cialis also X-linked recessive genetic male incidence, female transmission. Onset between the ages of more than 5-20, the performance with the Duchenne type similar but more benign course of disease, when 12-year-old can still walk, but 15-20 years after onset are mostly unable to walk. Cardiac involvement and mental retardation rather rare.
3, Erd muscular dystrophy: also known as limb-girdle muscular dystrophy, and autosomal recessive inheritance, gender may be the pathogenesis. Between the age of onset more than 20-30, mainly involving the proximal muscles, often the first affected upper limb, lower limb for many years after the impact. Occasional false gastrocnemius hypertrophy.
4, Landouzy-Dejerine muscular dystrophy: also known as Noodles scapulohumeral muscular dystrophy, and autosomal dominant inheritance, gender may be the pathogenesis. Usually at puberty onset, first of all affect the face and shoulder girdle muscles, showed special “myopathy face”, upper eyelid droop slightly, the amount of shallow patterns and nasolabial fold, table movements weaker, upper elevation difficult. Inspection can be found frown, drum gills, eyes closed, close-mouthed are weak, deltoid, biceps, muscular atrophy brachioradial obvious.
5, the other also distal, ocular, oculopharyngeal muscular dystrophy, etc., but are rare.
Progressive muscular dystrophy mainly depend on the diagnosis of symptoms, muscle enzyme tests such as EMG. Serum creatine phosphokinase (CPK), lactate dehydrogenase (LDH), myoglobin (Mb), aspartate cialis da 5 mg aminotransferase (GOT) and many other muscle enzymes were significantly increased; EMG icon myogenic damage; if necessary muscle biopsy can be clearly diagnosed.
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