Vaccinazioni per l’infanzia ed autismo: un caso accertato negli
Stati Uniti
Mercoledì 9
Aprile 2008 - Gli studi clinici hanno fallito nel mostrare un
legame tra vaccinazione ed autismo, ma molti genitori di bambini
autistici hanno nutrito dubbi su queste conclusioni.
Il Governo americano ha ora ammesso che la
vaccinazione può avere arrecato
danni ad una bambina di 9 anni, ed ha annunciato che si farà
carico delle spese per la cura.
Nel 2000 Hannah aveva 19 mesi ed uno sviluppo normale, quando
ricevette 5 iniezioni per la prevenzione di 9 malattie
infettive.
Nel 2001 alla bambina è stato diagnosticato il disturbo
autistico.
Per il fatto che il padre di Hannah era un neurologo al Johns
Hopkins Hospital, la bambina è stata sottoposta ad una serie di
esami, che hanno evidenziato un disordine a livello
mitocondriale.
Due teorie sono state ipotizzate: la prima che la bambina
presentava una sottostante malattia mitocondriale e che la
vaccinazione ha slatentizzato, la seconda è che la vaccinazione
ha
causato questo disordine.
Il Governo ha optato per la prima ipotesi: la bambina aveva una
sottostante malattia mitocondriale che è stata aggravata dalla
vaccinazione.
Molti dei vaccini che Hannah ha ricevuto contenevano Tiomersale,
un preservativo a base di Mercurio.
Negli Stati Uniti, il Tiomersale è stato rimosso dai vaccini
somministrati nell’infanzia a partire dal 2001.
Rimane aperto il dibattito sulle vaccinazioni multiple
nell’infanzia. ( Xagena Medicina )
Fonte: The New York Times, 2008 -
Medicina-Online.net + vedi
Autismo - La prova dei
Danni dei Vaccini +
Autismo dai VACCINI
|
Table
VII: Summary of Unusual Behaviors
in
Mercury-Poisoned Animals and Humans & in Autism
|
| Mercury
Poisoning |
Autism |
| Stereotyped
sniffing (rats) |
Stereotyped,
repetitive behaviors |
| Hyperactivity
(rats); poor response inhibition (humans), restlessness |
Hyperactivity;
ADHD-traits |
| Agitation
(humans) |
Agitation |
| Insomnia;
difficulty falling asleep (humans) |
Insomnia;
difficulty falling or staying asleep |
| Eating
disorders: anorexia, poor
appetite, food aversion, narrow food preferences, decided food
preferences (salty food) (humans) |
Eating
disorders: anorexia;
restricted diet/narrow food preferences; feeding and suckling problems |
| Masturbation,
priapism (children) |
Masturbatory
tendencies |
| Unintelligible
cries; continuous crying; unprovoked crying (infants and children) |
Unprovoked
crying |
| Self
injurious behavior, including head banging and hitting the head
(toddlers and children) |
Self
injurious behavior, including head banging and hitting the head |
| Grimacing
(children) |
Grimacing |
| Staring
spells (infants and children) |
Staring
spells |
g. Vision
In
autism, one of the earliest signs detected by mothers is a lack of eye
contact (Gillberg & Coleman, 1992), and an early diagnostic behavior
is failure to engage in joint attention based on the ability to “look
where you are pointing” (CHAT, Baron-Cohenet al, 1992).
Of 11 autistic children studied, ten had inaccurate or slow
visual saccades (Rosenhall et al, 1988).
Although some adults with ASD report exceptional visual acuity,
visual problems are common, with two separate studies reporting 50% of
ASDsubjects having some type of unusual visual impairment (Steffenburg,
in Gillberg & Coleman, 1992). Ritvo
et al (1986) and Creel et al (1989) found decreased function of the rods
in a study of autistic people, including a retinal sheen, and noted that
many such individuals tend to use peripheral vision because of this.
A number of case reports describe over-sensitivity to light and
blurred vision (Sperry, 1998; Gillberg & Coleman, 1992, p.29;
O’Neill & Jones, 1997).
Mercury can
lead to a variety of vision problems, especially in children (Pierce et
al, 1972; Snyder, 1972). Children
who ate high doses of mercury from contaminated pork developed blindness
(Snyder, 1972). In Iraqi
babies exposed prenatally there was blindness or impaired vision
(Amin-Zaki,1974 and 1979). Iraqi
children exposed postnatally developed visual disturbances, which ranged
from blurred or hazy vision to constriction of the visual fields to
complete blindness (Amin-Zaki et al, 1978).
Two girls with mercury vapor poisoning were found to have visual
field defects (Snyder, 1972), and, as previously noted, one child with
Hg poisoning developed gaze avoidance (Fagala & Wigg, 1992).
Acrodynia sufferers report vision problems, including
near-sightedness and light sensitivity or photophobia (Diner and
Brenner, 1998; Neville Recollection, Pink Disease site; Farnesworth,
1997; Matheson et al, 1980; Aronow and Fleischmann, 1976).
A 25 year old man with elemental mercury poisoning exhibited
decreased visual acuity, difficulty with visual fixation, and
constricted visual fields (Kark et al, 1971).
In Japanese victims, there was blurred vision as well as
constriction of visual fields (Snyder, 1972; Tokuomi et al, 1982). Iraqi mothers exposed to Hg had visual disturbance
(Amin-Zaki, 1979).
In dogs
exposed to daily doses of methylmercury, distortion of the visual evoked
response from the visual cortex was the first sign.
Damage occurred in the preclinical silent stage, demonstrating
that CNS damage is occurring before overt symptoms appear (Mattsson et
al, 1981). Monkeys treated
at birth with low level methylmercury exhibited impaired spatial vision
and visual acuity at age 3 and 4 years (Rice and Gilbert, 1982).
Disturbances caused by methylmercury in rat optic nerves were
observed (Kinoshita et al, 1999).
Table
VIII: Summary of
Visual Impairments Seen
in Mercury Poisoning & Autism
|
| Mercury
Poisoning |
Autism |
| Lack
of eye contact; difficulties with visual fixation |
Lack
of eye contact; gaze abnormalities; problems in joint attention |
| “Visual
impairments,” blindness, near-sightedness, decreased visual
acuity |
“Visual
impairments”; inaccurate or slow saccades; decreased functioning
of the rods; retinal sheen |
| Light
sensitivity, photophobia |
Over-sensitivity
to light |
| Blurred
or hazy vision |
Blurred
vision |
| Constricted
visual fields |
Not
described |
h. Physical
Presentations
There
is a much higher rate of autism among children with cerebral palsy than
would be expected by chance (Nordin and Gillberg, 1996).
Many autistic children have abnormal muscle tone including hyper-
and hypotonia, and many are incontinent or have difficulty being toilet
trained (Filipek et al, 1999; Church and Coplan, 1995).
Several of the infants which Teitelbaum and colleagues (1998)
observed showed decreased arm strength, and Schuler (1995) describes
greater muscle weakness in the upper than the lower body.
Impairments in oral-motor function, including problems chewing and
swallowing, are common, as noted previously.
These
impairments are seen in mercurialism as well. In the Iraqi and Japanese
epidemics, many children developed clinical cerebral palsy (Amin-Zaki,
1979; Myers & Davidson, 1998; Gilbert & Grant-Webster 1995; Dale,
1972). Amin-Zaki et al (1978)
reported muscle wasting and lack of motor power and control in most cases,
complete paralysis in several cases, and athetotic movements in 2 cases,
of postnatally exposed children. In
the Iraqi babies and children, some had increased muscle tone, while
others had decreased muscle tone. Abnormal
reflexes, spasticity, and weakness were common.
One child said “my hands are weak and do not obey me”
(Amin-Zaki et al, 1974 and 1978). The 12 year old who inhaled mercury
vapor exhibited weakness and decreased muscle strength (Fagala and Wigg,
1992). As in autism, muscle weakness from mercury poisoning is most
prominent in the upper body (Adams et al, 1983). Acrodynia, for example,
is marked by poor muscle tone in general and loss of arm strength in
particular (Farnesworth, 1997). Finally, difficulty in chewing and
swallowing, salivation, and drooling are common in children as well as
adults; incontinence was observed in children in the Iraqi Hg-crisis
(Amin-Zaki, 1974 and 1978; Pierce et al, 1972; Snyder, 1972; Joselow et
al, 1972; Smith, 1977).
The presence of rashes and dermatitis is sometimes reported in
descriptions of ASD subjects. Whiteley et al (1998) found that 63% of the ASD children had
a history of eczema or other skin complaints.“Some children with autism
are frequent scratchers. Gentle rubbing and scratching can become a
calming self-stimulation; but when it becomes clawing, and there are
rashes and open scrapes on the skin, a tactile intolerance can be
responsible” (O’Neill, 1999).
Rashes and itching are common disturbances in mercury toxicity as well
(Kark et al, 1971). A 4 year
old with Hg poisoning developed an itchy, peeling rash on the extremities
(Florentine and Sanfilippo, 1991). Mercury
vapor inhalation caused a rash and peeling on the palms and soles of a
pre-adolescent (Fagala and Wigg, 1992).
An acrodynia victim described himself as a child as having severe
itching and a constant burning sensation at the extremities, resulting in
him rubbing his hands and feet raw (Neville Recollection, Pink Disease
Support Group). Acrodynia
symptoms in anadult poisoned by ethylmercury injection included pink
scaling palms and soles, flushed cheeks, and itching (Matheson et al,
1980). In acrodynia the skin
may be rough and dry, and the soles and palms are usually but not
necessarily red (Aronow and Fleischmann, 1976).
Thimerosal ingested by 44 year old man led to dermatitis (Pfab et
al, 1996).
In
autism, “signs of autonomic disturbance may be noticed at times,
including sweating, irregular breathing, and rapid pulse” (Wing and
Attwood, 1987). There may be elevated blood flow and heart rate (Ornitz,
1987). An increased incidence
of acrocyanosis has been observed in Asperger’s syndrome.
Acrocyanosis is an uncommon disorder of poor circulation in which
skin on the hands and feet turn red and blue; there is profuse sweating;
and the fingers and toes are persistently cold (Carpenter and Morris,
1991).
Sweating and
circulatory abnormalities are also common in some forms of mercury
poisoning. Acrodynia in
adults and children results in excessive sweating, poor circulation, and
rapid heart rate (Farnesworth, 1997; Matheson et al, 1980; Cloarec et al,
1995; Warkany and Hubbard, 1953). The
12 year old with mercury vapor poisoning sweated profusely, especially at
night (Fagala and Wigg, 1992), and elevated blood pressure has been
reported in exposed workers (Vroom and Greer, 1972).
Autonomic system abnormalities can be caused by disturbances in
acetylcholine levels, known to be deficient in both autism and Hg
poisoning (see neurotransmitter section below).
|
Table
IX: Physical
Disturbances
in
Mercury Poisoning & Autism |
| Mercury
Poisoning |
Autism |
| Increase
in cerebral palsy; hyper- or hypotonia; paralysis, abnormal
reflexes; spasticity; decreased muscle strength and motor power,
especially in the upper body; incontinence; problems chewing,
swallowing, and salivating |
Increase
in cerebral palsy; hyper- or hypotonia; decreased muscle strength,
especially in the upper body; incontinence/toilet training
difficulties; problems chewing and swallowing |
| Rashes,
dermatitis, dry skin, itching; burning sensation |
Rashes,
dermatitis, eczema; itching |
| Autonomic
disturbances: excessive
sweating; poor circulation; elevated heart rate |
Autonomic
disturbances: sweating
abnormalities; poor circulation; elevated heart rate |
j. Gastrointestinal
Function
Many
if not most autistic individuals have gastrointestinal problems, the
most common complaints being chronic diarrhea, constipation,
gaseousness, and abdominal discomfort and distention (D’Eufemia et al,
1996; Horvath et al, 1999; Whitely et al, 1998).
Colitis is not uncommon (Wakefield et al, 1998).
As noted previously, anorexia is sometimes associated with ASD
(Gillberg & Coleman, 1992). Kanner
noted that over half his initial cases had feeding difficulties and
excessive vomiting as infants (1943).
O'Reilly and Waring (1993) have described sulfur deficiencies in
autism, an effect of which can be clumping of proteins on the gut wall,
which is lined with sulfated proteins. The clumping can lead to
increased intestinal permeability, or leaky gut syndrome (Shattock,
1997), found in many autistic individuals (D'Eufemia, 1996). Some ASD
individuals have unusual opioid peptide fragments in urine; these
peptides are believed to enter the bloodstream due to a leaky gut and to
resultfrom an incomplete breakdown of gluten and casein in the diet
possibly arising from "inadequacy of the [endopeptidase] enzyme
systems which are responsible for their breakdown" (Shattock,
1997).
Mercury, which
binds to sulfur groups (Clarkson, 1992), is known to cause
gastroenteritis (Kark et al, 1971).
For example, a four year old with diarrhea was initially
diagnosed with gastroenteritis (Florentine and Sanfilippo, 1991).
A pre-adolescent with mercury vapor poisoning developed nausea,
abdominal pain, poor appetite, rectal itching, and diarrhea; she
frequently strained to have a bowel movement, and was at one point
diagnosed with colitis (Fagala and Wigg, 1992).
Acrodynia is marked by both constipation and diarrhea (Diner and
Brenner, 1998). Incontinence
of urine and stool are observed in infants and children exposed pre- and
postnatally in Iraq (Amin-Zaki, 1974 and 1978).
In another case, a 28 year old woman with occupational exposure
to mercury vapor developed watery stools (Ross et al, 1977).
Diarrhea and digestive disturbance were seen in a dentist with
measurable mercury levels; there was obesity in another dentist (Smith,
1977). A 44 year old man
poisoned with thimerosal given intramuscularly developed
gastrointestinal bleeding, which looked like hemorrhaging colitis
(Lowell et al, 1996). Intense
exposure to mercury vapor can cause abdominal pain, nausea, and vomiting
(Feldman, 1982). Severe
constipation, anorexia, weight loss, and other “disturbances of
gastrointestinal function” have been noted in other cases (Adams et
al, 1983; Joselow et al, 1972). Rats
tested with mercuric chloride were observed with “lesions of the ileum
and colon with abnormal deposits of IgA in the basement membranes of the
intestinal glands and of IgG in the basement membranes of the lamina
propria” (Andres, 1984, reviewed in EPA, 1997, p.3-36).
In another rat experiment, Hg was found to increase the
permeability of intestinal epithelial tissues (Watzl et al, 1999).
Mercury also inhibits the peptidase - dipeptidyl peptidase IV -
which cleaves, among other substances, casomorphin during the
digestive process (Puschel et al, 1982).
There is no
reported increase in incidence in kidney problems in autism.
Although renal function is commonly impaired from Hg exposure,
such impairment would not be expected if the mercury exposure occurred
from thimerosal injections, since kidney function may be unaffected when
mercury is injected or inhaled (Davis et al, 1994; Fagala and Wigg,
1992). For example,
although thimerosal ingested orally by a 44 year old man resulted in
renal tubular failure and gingivitis (Pfab et al, 1996), renal function
was normal in another 44 year old man injected intramuscularly with
thimerosal (Lowell et al, 1996).
Table
X: Summary of
Gastrointestinal Problems in
Mercury Poisoning & Autism
|
| Mercury
Poisoning |
Autism |
| Gastroenteritis,
diarrhea; abdominal pain, rectal itching, constipation,
“colitis” |
Diarrhea,
constipation, gaseousness, abdominal discomfort, colitis |
| Anorexia,
weight loss, nausea, poor appetite |
Anorexia;
feeding difficulties, vomiting as infants |
| Lesions
of the ileum and colon; increased intestinal permeability |
Leaky
gut syndrome from sulfur deficiency |
| Inhibits
dipeptidyl peptidase IV, which cleaves casomorphin |
Inadequate
endopeptidase enzymes responsible |
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