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Huntington chorea (fā)the age of illness is 35 ～44at the age of 15 ～18year 。about 25% of patients develop after 50 or even 70 years old (fā)sick ，clinical manifestations (xi ton)lighter. there are three main characteristics: abnormal movement ，intelligence decline and mental abnormalities.

most (shù)patient's initial manifestations (xi ton)for detailed action (xi and)cannot adjust ，light involuntary movement, sound barrier ，hypertension of tendon reflexes, losing planning in daily life ，memory decreases (being aware of impairment sometimes precedes the impairment )，decreased attention ，depression and irritability 。rapidly (fā)shows a clear dance movement for purposeless 、no rules (guī)the body, face and body movement ，performance (xi ton)to sniff, pout, and toss 、sailing shoulders 、the body is tilted forward and backward, dancing and so on ，emotional excitement and tension worsen, and disappear during sleep 。it's even more difficult to move casually ，eye anomalies include rapid eye swiping and gazing disorders ，difficulty swallowing, most of them (shù)patients lose their ability to work ，response torch, visual space ability decline, language barrier ，lack of self-control ，personality change ，delusion ，sometimes the situation cannot be controlled ，have active behavior;

performance of advanced patients (xi ton)for sports noise, straightness and irritation ，difficulty swallowing ，difficulty in action ，, body binding sign ，behavior is more severe ，can't take care of yourself 。juvenile patients developed before the age of 21 (fā)sick ，mostly passed down by patriarchal lines and clinical manifestations (xi ton)different from adult type ，mainly for reducing movement, straightening ，hyperreflexia ，anomaly of eye movements ，severe intellectual decline ，30～50%patients appear (xi ton)injection (fā)the course of the disease progresses quickly 。

huntington disease (fā)born in middle-aged people, i met children and teenagers ，both men and women may suffer from illness. send (fā)disease hiding ，slow progressive aggravation ，average survival time of 10 ～20 year. clinical main manifestations (xi ton)involuntarily for dance 、mental disorders and progressive disorders are called "three connections" (li ton)confirmation” 。middle age develop (fā)the patients mainly use dance movements and gradually emerge (xi ton)impatient and mental disorders; childhood and adolescence (fā)patients are mostly suffering from muscle dysfunction ，often accompanied by incision and communist misconduct 。

sports disorders

progressive development (fā)the performance of sports disorders (xi ton)for all limbs 、noodle 、it's done suddenly 、quick jump or pull ，these movements are not known in advance ，uncontrollable ，can also express (xi ton)for uncontrollable slow movement 。check the body (fā)now (xi ton)involuntary movements and reduced muscle strength in dance 。involuntary movement of dance is a prominent feature of this disease ，most of them start to show (xi ton)a short, uncontrollable ghost face 、point and finger flexion and stretching ，similar to painless twitching, but slower and non-steretic 。depending on the condition of the disease (fā)exhibit, no casual movement progressive aggravates ，appear (xi ton)typical eyebrow lift and head flexion ，when the object is taken, the head moves and the patient appears while walking. (xi ton)unstable (wěn)，teng jumps to the pace (t toi)，plus the posture of constantly changing hands ，the whole body movement is like a dance 。in the later stage of the disease, patients cannot stand or walk due to involuntary movement of the whole body. 。even if you sit, you won't be ashamed (wěn)，twist, suddenly stood up and sat down ，the trunk and limbs are still twisting behind the bed 。when the condition is (fā)exhibition ，free movement is more severe (fā)clearly ，clumsy, erratic 、stiff, unable to maintain repetitive and casual movement ，appear (xi ton)difficulty swallowing 、talk and stuttering 。appear (xi ton)abnormal eye activity is abnormal. can occur in the late stages of the disease (xi ton)wooden stumbling state where limbs cannot move (t toi)。

dance-like exercise disorders are typical of adult huntington disease (xi ton)。20juvenile patients who started before age (5% of huntington's disease ～10%)，inactive muscle straightening is the main dysfunction; manifestations (xi ton)strong muscle 、skin dysfunction ，in the late stage, it will be horned bow reversed 。in addition, it is different from adult patients ，about 50% of juvenile huntington patients have systemic invasion (fā)do 。

knowledge obstacles

progressive dysfunction is another characteristic of patients with huntington disease 。in the early stage, there are characteristics of under-cortical dysfunction ，later performance (xi ton)for mixed schizophrenia and schizophrenia 。

identical disorders can occur in the early stages of huntington disease (xi ton)。start to show (xi ton)because memory and computing power in daily life and work are reduced, patients only suffer from mild damage when they remember new information. ，but the memory has significant flaws. due to the fluency of the words 、decreased in the ability to judge social and human relations ，the patient changes are more confusing. changes in words ，including speaking not fluent ，difficulty in finding words and sound disorders ?？su Z fluent damaging is one of the premature cognitive dysfunctions of huntington's disease 。in the middle and late stages of illness ，patients cannot complete naming tests that require reminiscence of infrequently used terms. dance-like exercise disorder? ？shanhuan bar zinc pain sword taxation l(fā)the rhythm and agility of sound ，it hinders the amount of words 、speed 、seminar (ji and)the length of the law and short words make the spoken language appear (xi ton)a kind of turbulence (fā)characteristics ，therefore ，stylistic and erectile dysfunction are outstanding characteristics of patients with this disease 。because the patient still retains the recognition memory of the verb, the ability to identify the opponent and the naming of the object, huntington disease patients can continue (xù)communicate with people 。

depending on the condition of the disease (fā)expand, attention and discrimination 。planning and connection required (xù)arrange information (y and)i felt particularly difficult. decreased visual space capability ，there is difficulty in judging the structure. response to the leaf (zh the)the line function will appear (xi ton)obstacles 。

mental disorders

emotional disorders are common mental disorders, including anxiety 、nervous 、excited and angry 、or indifferent 、or disorganized and interest reduction ，and more often (xi ton)in sports disorders (fā)before birth 。due to emotional disorders (xi ton)before the patient's movements ，so it's not a reactive mental disorder but a manifestation of the disease itself (xi ton)。depression and dysfunction (fā)the birth rate is also very high ，if the patient's severe depression symptoms can develop early (fā)now (xi ton)and treat it in time ，it can prevent self-killing. huntington patients may also appear (xi ton)changes in personality behavior ，appear (xi ton)antisocial behavior, schizophrenia 、negative (zh the)crazy and fantasy 。

huntington's disease in adolescent

onset in children and adolescence ，20 about 10% of the disease started before age ，age less than 4 years old starts at about 5% 。clinical manifestations (xi ton)different from adult huntington disease ，the course of the disease progresses faster ，myocardial dysfunction is a prominent manifestation (xi ton)，often replace dance sports with straightforwardness 。parkinson's comprehensive sign 、brain-sexual commonal disorder 、eyeball movement abnormally 、skin ablation and inflammation (fā)can appear (xi ton)mental decline and abnormal behavior ，some patients' performance (xi ton)excessive movement 。a few (shù)the movement of the case is atypical ，performance (xi ton)progressive muscle straightness and exercise reduction, dance-hand and foot slight movements are unknown ，most of them were found in childhood or before the age of 20 (fā)sick person. implantation and brain-sexual communal disorders are also common characteristics of adolescents ，clinic and family history can prompt diagnosis 。

overall come ，if you have the following symptoms, you must be vigilant:

1.anomalous emotions

become cold 、irritable or depressed 、language barriers 、stubborn temper.

2.finger 、legs 、appearance on the face or body (xi ton)involuntarily

(1)early abnormal eye movements.

(2)facial prolonged and contracted muscles in the middle stage 、the anomaly of the horn and back; involuntary movement; walking 、balance appears (xi ton)obstacles; dance movements 、torsional movement 、twitch 、stop the silence (wěn)inconsistent pace (t toi);it is difficult to do activities that require cleverness; unable to control the speed and strength of the movement; reaction is irritating; powerlessness throughout the body; weight reduction, etc. 。

(3)late physical stiffness; exercise xu xu ，start (fā)or persist (xù)difficulty in movement; dramatic dance; severe weight drop; inability to walk; inability to speak; inability to swallow ，there is danger of being choked; life is completely unbearable 。

3.intellectual deterioration

judgment force 、memory and awareness ability are reduced.

huntington dance is a traditional neurosis (jīng)degenerative diseases ，commonly seen in adults aged 20-50 ，main manifestations (xi ton)dance for the siblings and dance ，multiple ，blink ，involuntary movements increase when sticking out tongue 。huntington dance patients recommend eating less meat and more vegetables 、fruits, such as: green vegetables 、celery, banana, etc. ，not only contains many vitamins ，and rich in trace elements and minerals 。avoid eating foods that are prone to heat; eat less foods that are high in vitro sterol; eat less foods that are caused by oil ；the internal organs should be reduced 、seafood, etc.; eat less spicy 、numb 、spicy ingredients such as sausage 。 the iron in the meat exists in the form of redox ，not affected by other food factors ，high bioavailability ，can replenish 。

translation testing

translation testing is an important means of diagnosis of huntington chorea ，PCR law detection IT5 in genes CAG re-copy number (shù)，no more than 38 copies of normal people ，there are more than 39 patients ，not yet found (fā)now (xi ton)repeat the plot (xi ton)high syrup rate ，just test the patient ，can undergo pre-disease diagnosis and treatment (chǎn)pre-diagnosis, etc. 。

brain picture

the brain image may have a diffuse and abnormality without any distinction 。mainly low-amplitude fast waves, especially the size of ye ming ，anomaly account for 88.9% 。αreduce or lose activities ，reduced amplitude 。visually intimate (fā)potential amplitude decreases ，however, the first wave partial incubation period is normal ?；improper cheek length 100 ，test P300 it may be a target for early intelligent disability in this disease.

imaging inspection

head CT or MRI it has important clinical value for diagnosing huntington chorea ，a typical imaging feature is atrophy of the double-sided tail nucleus, which causes the outer side of the brain chamber to bulge outward. 。SPECT check (fā)now (xi ton)tail and bean nucleus (qū)blood lumens decreased ，blood flow from the altitude and top leaves also decreased ，it is related to the pathological changes in these parts of the patient. PET performance (xi ton)tail core area (qū)glucose induced decreases ，tail core area (qū)decreased cervical activity may occur (xi ton)before the tail nucleus atrophy.