Distinctive symptoms
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Register , to see more distinctive signs of diseases and studies — 100%
paroxysmal myoplegia
100%
43%
myotonia —
69%
Weakness is worse in the morning
55%
—
dystrophic myotonia —
49%
paralysis of the left leg
50%
—
neuromyotonia —
48%
paralysis of the right leg
50%
—
lags behind in the development —
43%
weakness in the morning
47%
—
childhood diseases —
43%
thirst
47%
—
logorrhea —
40%
hyperaldosteronism
46%
—
ganglioneuritis —
39%
paralysis right-sided
45%
—
steinert 's disease —
39%
ascending paralysis
43%
—
congenital myopathies —
39%
lot paralysis left-sided
42%
—
oppenheim syndrome —
39%
decrease in phosphorus
39%
—
metabolic disorder —
37%
paralysis of the limbs
71%
30%
sluggish baby —
37%
thirst attacks
38%
—
birth trauma of the head —
36%
increase in phosphorus
38%
—
weakness in the legs —
36%
increased sugar
37%
—
can not hold his head —
35%
hemiplegia
37%
—
muscle tension —
35%
increased potassium
66%
28%
perinatal encephalopathy —
35%
gynecomastia
35%
—
sucks the breast —
35%
bruising morning
34%
—
inflammatory myopathy —
34%
need for salt
34%
—
paretic gait —
34%
impotence
34%
—
head injury —
34%
monthly prolonged
34%
—
asymmetry —
33%
cramps in the extremities
33%
—
stiffness in the joints —
32%
sweating of the face
33%
—
sad —
32%
loves family
33%
—
lack of desires —
32%
glycogenoses
33%
—
hypoparathyroidism —
32%
hirsutism
32%
—
dystrophy —
31%
loss of strength in the morning
32%
—
stiffness of movements —
30%
weak ligaments
32%
—
weakness no —
30%
sweating with palpitations
31%
—
cannot relax —
30%
decreased magnesium
31%
—
fatigue from children —
30%
fatigue in the morning
31%
—
leg weakness walking —
30%
attacks of pain
31%
—
helps others —
30%
periodic paralysis
64%
31%
postencephalitic syndrome —
30%
increased hairiness
30%
—
delayed motor development —
29%
sweats often
30%
—
rickets —
28%
weakness of the ligaments
30%
—
paresis of legs —
28%
face is red
30%
—
weakness in the leg muscles —
28%
menstruation irregular
30%
—
cns tumors —
27%
hypotension with weakness
29%
—
trauma —
27%
slow onset of the disease
29%
—
neuroinfections —
27%
in the morning listlessness
29%
—
myxedema —
27%
muscle fatigue
28%
—
delayed reaction —
27%
absences
28%
—
delay in physical development —
26%
severe sweating
27%
—
muscle atrophy —
26%
tachycardia attacks
27%
—
delay of mental development —
25%
dependence on parents
27%
—
delayed speech development —
25%
increased profuse sweating
27%
—
nervous excitability —
25%
rapid breathing
27%
—
head tumor —
25%
severe exhaustion
27%
—
encephalopathy —
25%
neurological pain
26%
—
myotonia is congenital —
25%
hypoglycemia
26%
—
traumatic brain injury —
25%
hypotrophy
26%
—
children's speech —
24%
sensations in the extremities
26%
—
motor activity —
24%
hysteria
26%
—
no children —
24%
somatoform dysfunction of the autonomic nervous system
26%
—
mental retardation —
24%
epilepsy attacks
25%
—
increased motor activity —
24%
epilepsy
24%
—
high height —
23%
rapid reaction
24%
—
brain tumor —
23%
neurosis
24%
—
organic brain damage —
22%
general weakness
24%
—
joint diseases —
21%
sweating is increased
24%
—
weakness after illness —
21%
liquid stool
24%
—
brain damage —
21%
constant weakness
24%
—
stage of recovery —
20%
diarrhea
23%
—
recovery period —
20%
tachycardia
23%
—
swelling —
20%
hypotension
23%
—
drug disease —
19%
worse in morning
23%
—
oncology —
18%
thin
23%
—
inflammation —
18%
convulsions
22%
—
rossolimo-steinert-kurschmann dystrophic myotonia —
17%
feeling of bruising
22%
—
damage to the nervous system
21%
34%
palpitations
22%
—
neurological disorders
21%
29%
vomiting
22%
—
paresis
24%
32%
increased
41%
18%
up circulatory disorders
21%
—
gastrointestinal problems
21%
—
onset of illness
20%
—
paralysis
54%
33%
gamstorp disease
18%
—
lowered
42%
25%
paralysis of the lower extremities
44%
30%