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Comparison results

 
Results: Differences General ✘Sluggish child syndrome✘Myotonic syndrome in children
Related research Analogs Analogs
Register, to see more distinctive signs of diseases and studies 84%(5)—
Elements and vitamins 43%(1)—
MRI of the organ —39%(0)
CT of the organ —38%(0)
Thyroid hormones —28%(1)
MRI of the brain —23%(0)
Neurologist's examination —22%(0)
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% —
myotonia — 69%
increased ldh 84% —
dystrophic myotonia — 49%
hoffmann 's perifolliculitis 64% —
neuromyotonia — 48%
werdnig-hoffman amyotrophy 58% —
paroxysmal myoplegia — 43%
galactosemia 58% —
logorrhea — 40%
spinal amyotrophy 58% —
steinert 's disease — 39%
ganglioneuritis 94% 39%
relaxation — 37%
oppenheim syndrome 94% 39%
birth trauma of the head — 36%
congenital myopathies 94% 39%
can not hold his head — 35%
inflammatory myopathy 83% 34%
perinatal encephalopathy — 35%
hypotension 47% —
muscle tension — 35%
cerebral palsy 43% —
paretic gait — 34%
weakness is worse from movement 40% —
head injury — 34%
facial muscle weakness 39% —
asymmetry — 33%
phenylketonuria 38% —
hypoparathyroidism — 32%
weakness in the hip 36% —
paresis — 32%
rapid reaction 36% —
stiffness in the joints — 32%
worse from movement 35% —
sad — 32%
weakness in the foot 35% —
dystrophy — 31%
myasthenia 35% —
periodic paralysis — 31%
spinal cord injury 34% —
stiffness of movements — 30%
marfan syndrome 34% —
helps others — 30%
strongest weakness 34% —
paralysis of the limbs — 30%
glycogenoses 34% —
paralysis of the lower extremities — 30%
down syndrome 33% —
postencephalitic syndrome — 30%
impaired function of the cerebral hemispheres 33% —
leg weakness walking — 30%
mitochondrial myopathy 32% —
fatigue from children — 30%
increase in creatine kinase 32% —
cannot relax — 29%
muscular dystrophy 31% —
hormonal disorders — 29%
weak joints 30% —
delayed motor development — 29%
hypotension with weakness 30% —
neurological disorders — 29%
hyperkinesis 30% —
weakness in the hands — 28%
intellectual disabilities in children 29% —
increased potassium — 28%
spinal injury 29% —
paresis of legs — 28%
smart baby 28% —
myxedema — 27%
inflammation of the brain 27% —
neuroinfections — 27%
muscle hypertonus 27% —
delay in physical development — 27%
hypotension 27% —
delayed reaction — 27%
cognitive disorders 26% —
cns tumors — 27%
traumatic illness 25% —
weakness in the extremities — 26%
calculating 25% —
delay of mental development — 25%
patient is motionless 24% —
head tumor — 25%
spasm 24% —
nervous excitability — 25%
inflammation 44% 18%
myotonia is congenital — 25%
impaired arterial function 21% —
encephalopathy — 25%
nemaline myopathy 19% —
traumatic brain injury — 25%
myopathy 63% 44%
children's speech — 24%
flaccid paralysis syndrome 49% 32%
delayed speech development — 24%
muscle atrophy 40% 26%
motor activity — 24%
sluggish baby 50% 38%
no children — 24%
childhood diseases 47% 43%
increased motor activity — 24%
brain tumor — 23%
high height — 23%
overexcitation of the psyche — 23%
organic brain damage — 22%
quickly gets tired — 21%
joint diseases — 21%
recovery period — 20%
stage of recovery — 20%
periodic illness — 20%
swelling — 20%
drug disease — 19%
oncology — 18%
rossolimo-steinert-kurschmann dystrophic myotonia — 17%
lags behind in the development 33% 43%
weakness in the legs 28% 36%
lowered 19% 25%
trauma 21% 27%
metabolic disorder 33% 37%
damage to the nervous system 30% 34%

Instructions

Video
  1. Introduce new diseases through 🔍 Search and input on the top panel using
  2. The table shows the most important distinguishing symptoms, tests and diagnoses related to the selected diseases.
  3. The higher the percentage, the more important this symptom is for the disease and vice versa. At 0%, we can say that this symptom never occurs in the disease.
  4. The list changes dynamically depending on the data of the current visit in the selection of therapy .
  5. Click on the percentageto see the suggestions from the original source.
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