Distinctive symptoms
Register , to see more distinctive signs of diseases and studies 100% —
Register , to see more distinctive signs of diseases and studies — 100%
myotonia
69%
—
retinitis pigmentosa —
89%
dystrophic myotonia
49%
—
lawrence-moon-bardet-bidl syndrome —
85%
neuromyotonia
48%
—
retinitis —
78%
myopathy
44%
—
lawrence-moon-beadle syndrome —
77%
paroxysmal myoplegia
43%
—
polydactyly —
76%
logorrhea
40%
—
myopic chorioretinitis —
73%
oppenheim syndrome
39%
—
congenital anomalies of the upper extremities —
72%
congenital myopathies
39%
—
syndactyly —
68%
steinert 's disease
39%
—
congenital anomalies of the lower extremities —
62%
ganglioneuritis
39%
—
agenesis of the corpus callosum —
61%
sluggish baby
38%
—
hypogonadism —
60%
muscle weakness
38%
—
congenital myopia —
59%
relaxation
37%
—
senile hyperopia —
55%
weakness in the legs
36%
—
fundus arteries narrowed —
53%
birth trauma of the head
36%
—
up vascular mesh —
51%
muscle tension
35%
—
vitamin c increased —
51%
can not hold his head
35%
—
not mindfulness —
50%
perinatal encephalopathy
35%
—
obesity —
50%
head injury
34%
—
limited vocabulary —
50%
paretic gait
34%
—
teacher —
49%
damage to the nervous system
34%
—
progressive myopia —
49%
inflammatory myopathy
34%
—
hyperopia —
48%
paralysis
33%
—
astigmatism —
48%
asymmetry
33%
—
brachydactyly —
48%
paresis
32%
—
patient is motionless —
48%
stiffness in the joints
32%
—
deformity of the toes —
48%
sad
32%
—
diabetes mellitus —
47%
hypoparathyroidism
32%
—
deformity of the fingers —
47%
flaccid paralysis syndrome
32%
—
obesity on the stomach —
46%
periodic paralysis
31%
—
abdominal obesity —
46%
fatigue from children
30%
—
dystrophy
31%
76%
paralysis of the lower extremities
30%
—
anomalies of kidney development —
44%
paralysis of the limbs
30%
—
fat deposits —
43%
postencephalitic syndrome
30%
—
myopia —
42%
stiffness of movements
30%
—
strabismus —
42%
leg weakness walking
30%
—
deformity of fingers —
42%
weakness no
30%
—
skeletal deformity —
42%
delayed motor development
29%
—
deformity of the foot —
41%
cannot relax
29%
—
shortening of legs —
41%
hormonal disorders
29%
—
speech absence —
40%
rickets
28%
—
angiopathy of the retina —
40%
weakness in the leg muscles
28%
—
cataract —
40%
increased potassium
28%
—
hyperlipidemia —
39%
paresis of legs
28%
—
cholesterolemia —
39%
weakness in the hands
28%
—
decreased intelligence —
39%
myxedema
27%
—
curvature of the legs —
38%
neuroinfections
27%
—
s eyes cloudy —
38%
delayed reaction
27%
—
will not work —
37%
delay in physical development
27%
—
weight change —
37%
trauma
27%
—
ataxia —
37%
cns tumors
27%
—
speech slurred —
36%
muscle atrophy
26%
—
bone deformation —
36%
weakness in the extremities
26%
—
arterial occlusion —
35%
encephalopathy
25%
—
overweight —
35%
myotonia is congenital
25%
—
impaired coordination —
35%
nervous excitability
25%
—
decreased concentration of attention —
35%
delay of mental development
25%
—
visual impairment —
34%
traumatic brain injury
25%
—
convulsions —
33%
head tumor
25%
—
control issues —
32%
increased motor activity
24%
—
angiopathy —
31%
motor activity
24%
—
inflammation
18%
48%
no children
24%
—
there are no complaints —
30%
brain tumor
23%
—
mental retardation
24%
53%
high height
23%
—
delayed speech development
24%
53%
overexcitation of the psyche
23%
—
children's speech
24%
52%
organic brain damage
22%
—
increased
18%
38%
weakness after illness
21%
—
neurological disorders
29%
45%
joint diseases
21%
—
lowered
25%
39%
quickly gets tired
21%
—
lags behind in the development
43%
57%
periodic illness
20%
—
recovery period
20%
31%
swelling
20%
—
stage of recovery
20%
31%
drug disease
19%
—
oncology
18%
28%
rossolimo-steinert-kurschmann dystrophic myotonia
17%
—
metabolic disorder
37%
46%
childhood diseases
43%
30%
helps others
30%
33%