Distinctive symptoms
Register , to see more distinctive signs of diseases and studies 100% —
Register , to see more distinctive signs of diseases and studies — 96%
congenital myopathies
94%
—
weakness in the arms and legs —
90%
hysterical
92%
—
weakness of the muscles of the hands —
89%
oppenheim syndrome
92%
—
neurological disorders —
80%
ganglioneuritis
90%
—
hypotrophy —
76%
increased ldh
85%
—
vibration sickness —
74%
inflammatory myopathy
83%
—
tremor —
73%
hoffmann 's perifolliculitis
64%
—
weakness in the legs
28%
100%
myopathy
62%
—
thin —
68%
galactosemia
58%
—
skin anesthesia —
67%
werdnig-hoffman amyotrophy
58%
—
weakness in the leg muscles
31%
98%
sluggish baby
50%
—
distal motor neuropathy —
67%
hypotension
47%
—
nbsp —
66%
flaccid paralysis syndrome
47%
—
thin limbs —
66%
inflammation
44%
—
weakness in the extremities —
64%
cerebral palsy
43%
—
анестезия —
63%
facial muscle weakness
39%
—
weakness in the knees —
62%
weakness is worse from movement
39%
—
weakness of the fingers —
60%
phenylketonuria
38%
—
weakness in the wrists —
58%
weakness in the hip
36%
—
weakness in the shoulder —
56%
rapid reaction
36%
—
tremor in the legs —
56%
myasthenia
35%
—
hypotension with hypotrophy —
56%
weakness in the foot
35%
—
intermittent lameness —
55%
worse when moving
35%
—
skinny legs —
55%
marfan syndrome
34%
—
progressive bulbar paralysis —
54%
strongest weakness
34%
—
tremor of the limb —
54%
paralysis
34%
—
dystrophy —
54%
glycogenoses
34%
—
loss of touch —
53%
weakness no
33%
—
anomalies of labor activity —
52%
spinal cord injury
33%
—
myelopathy —
51%
down syndrome
33%
—
muscle atrophy
40%
90%
lags behind in the development
33%
—
tremor of the hands —
49%
increase in creatine kinase
32%
—
patient's condition —
45%
mitochondrial myopathy
32%
—
muscle weakness
41%
84%
rickets
31%
—
responsible —
40%
muscular dystrophy
31%
—
weakness after illness
22%
62%
weak joints
30%
—
damage to the nervous system
30%
69%
hyperkinesis
30%
—
family man —
39%
hypotension with weakness
30%
—
gradual deterioration of the condition —
39%
intellectual disabilities in children
29%
—
rapid weight loss —
38%
smart baby
28%
—
emaciation —
38%
hypotension
27%
—
presses —
36%
inflammation of the brain
27%
—
onset of illness —
33%
mental retardation
27%
—
skinny legs and arms —
30%
muscle hypertonus
26%
—
childhood diseases
47%
58%
cognitive disorders
26%
—
spinal amyotrophy
58%
66%
calculating
25%
—
metabolic disorder
33%
37%
traumatic illness
25%
—
patient is motionless
24%
—
spasm
23%
—
brain damage
22%
—
impaired arterial function
21%
—
trauma
21%
—
nemaline myopathy
19%
—