Distinctive symptoms
Register , to see more distinctive signs of diseases and studies 100% —
Register , to see more distinctive signs of diseases and studies — 100%
hysterical
95%
—
lethargy —
100%
ganglioneuritis
94%
—
encephalopathy —
92%
oppenheim syndrome
94%
—
epilepsy attacks —
90%
congenital myopathies
94%
—
epilepsy —
86%
increased ldh
84%
—
g93 4 unspecified encephalopathy —
86%
inflammatory myopathy
83%
—
convulsions —
79%
hoffmann 's perifolliculitis
64%
—
impaired nervous system function —
79%
myopathy
63%
—
infantile —
70%
galactosemia
58%
—
hypertension in a child —
63%
werdnig-hoffman amyotrophy
58%
—
apnea —
62%
spinal amyotrophy
58%
—
metachromatic leukodystrophy —
60%
sluggish baby
50%
—
history of liver surgery —
59%
flaccid paralysis syndrome
49%
—
fine motor skills are impaired —
58%
inflammation
44%
—
spastic paralysis —
56%
cerebral palsy
43%
—
muscle spasm of the hands —
54%
weakness is worse from movement
40%
—
protein with increased —
54%
muscle atrophy
40%
—
problems with the father —
51%
facial muscle weakness
39%
—
paralysis of the limbs —
51%
phenylketonuria
38%
—
breathing superficial —
50%
rapid reaction
36%
—
spasms in the body —
50%
weakness in the hip
36%
—
type of breathing is mixed —
49%
myasthenia
35%
—
epilepsy in children —
48%
weakness in the foot
35%
—
convulsive syndrome in children —
47%
worse from movement
35%
—
weak breathing —
47%
glycogenoses
34%
—
twitches eyelid —
46%
marfan syndrome
34%
—
twitching of the upper eyelid —
46%
strongest weakness
34%
—
porous skin —
45%
spinal cord injury
34%
—
skeletal deformity —
45%
metabolic disorder
33%
—
no consciousness —
45%
impaired function of the cerebral hemispheres
33%
—
weakness when breathing —
44%
down syndrome
33%
—
tics —
44%
weakness no
33%
—
lipoidosis —
44%
mitochondrial myopathy
32%
—
absences —
44%
increase in creatine kinase
32%
—
deformities of the limbs —
43%
muscular dystrophy
31%
—
damage to the nervous system
30%
73%
rickets
31%
—
diseases of infants —
42%
weakness in the leg muscles
31%
—
delay of mental development —
42%
weak joints
30%
—
history of surgery —
41%
hyperkinesis
30%
—
delayed speech development —
41%
intellectual disabilities in children
29%
—
protein reduced —
40%
spinal injury
29%
—
increased
19%
59%
weakness in the legs
28%
—
difficult to swallow —
40%
inflammation of the brain
27%
—
children's speech —
39%
mental retardation
27%
—
paresis —
38%
traumatic illness
25%
—
protein c deficiency —
38%
calculating
25%
—
not enough time —
37%
trauma
21%
—
dependence on the doctor —
36%
impaired arterial function
21%
—
acute condition —
35%
nemaline myopathy
19%
—
роды и вскармливание —
33%
childhood diseases
47%
32%
periodic illness —
33%
onset of illness —
32%
lowered
19%
51%
hypotension
27%
59%
weakness after illness
23%
49%
muscle weakness
41%
62%
lags behind in the development
33%
50%
hypotension with weakness
30%
46%
smart baby
28%
43%
muscle hypertonus
27%
40%
cognitive disorders
26%
39%
patient is motionless
24%
37%
spasm
24%
36%
hypotension
47%
51%
paralysis
36%
39%