Distinctive symptoms
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Register , to see more distinctive signs of diseases and studies — 100%
weakness in the arms and legs
90%
—
congenital myopathies —
94%
weakness of the muscles of the hands
89%
—
oppenheim syndrome —
92%
neurological disorders
80%
—
hysterical —
92%
hypotrophy
76%
—
ganglioneuritis —
90%
vibration sickness
74%
—
increased ldh —
85%
tremor
73%
—
inflammatory myopathy —
83%
weakness in the legs
100%
28%
hoffmann 's perifolliculitis —
64%
thin
68%
—
myopathy —
62%
skin anesthesia
67%
—
galactosemia —
58%
distal motor neuropathy
67%
—
werdnig-hoffman amyotrophy —
58%
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66%
—
sluggish baby —
50%
thin limbs
66%
—
flaccid paralysis syndrome —
47%
weakness in the leg muscles
98%
31%
hypotension —
47%
weakness in the extremities
64%
—
inflammation —
44%
анестезия
63%
—
cerebral palsy —
43%
weakness in the knees
62%
—
facial muscle weakness —
39%
weakness of the fingers
60%
—
weakness is worse from movement —
39%
weakness in the wrists
58%
—
phenylketonuria —
38%
tremor in the legs
56%
—
rapid reaction —
36%
hypotension with hypotrophy
56%
—
weakness in the hip —
36%
weakness in the shoulder
56%
—
myasthenia —
35%
intermittent lameness
55%
—
worse when moving —
35%
skinny legs
55%
—
weakness in the foot —
35%
progressive bulbar paralysis
54%
—
glycogenoses —
34%
tremor of the limb
54%
—
paralysis —
34%
dystrophy
54%
—
strongest weakness —
34%
loss of touch
53%
—
marfan syndrome —
34%
anomalies of labor activity
52%
—
spinal cord injury —
33%
myelopathy
51%
—
weakness no —
33%
tremor of the hands
49%
—
down syndrome —
33%
muscle atrophy
90%
40%
lags behind in the development —
33%
patient's condition
45%
—
increase in creatine kinase —
32%
muscle weakness
84%
41%
mitochondrial myopathy —
32%
responsible
40%
—
muscular dystrophy —
31%
family man
39%
—
rickets —
31%
gradual deterioration of the condition
39%
—
hyperkinesis —
30%
weakness after illness
62%
22%
weak joints —
30%
emaciation
38%
—
hypotension with weakness —
30%
rapid weight loss
38%
—
intellectual disabilities in children —
29%
damage to the nervous system
69%
30%
smart baby —
28%
presses
36%
—
hypotension —
27%
onset of illness
33%
—
inflammation of the brain —
27%
skinny legs and arms
30%
—
mental retardation —
27%
childhood diseases
58%
47%
muscle hypertonus —
26%
spinal amyotrophy
66%
58%
cognitive disorders —
26%
metabolic disorder
37%
33%
calculating —
25%
traumatic illness —
25%
patient is motionless —
24%
spasm —
23%
brain damage —
22%
impaired arterial function —
21%
trauma —
21%
nemaline myopathy —
19%