Distinctive symptoms
Register , to see more distinctive signs of diseases and studies 92% 10%
Register , to see more distinctive signs of diseases and studies — 35%
delayed speech development
69%
13%
hemiparesis —
27%
children's speech
66%
12%
epileptic status —
27%
lags behind in the development
59%
11%
cramps in the extremities —
25%
motor alalia
44%
—
epilepsy in childhood —
24%
underdevelopment
51%
7%
paralysis —
24%
delayed motor development
31%
—
brain tumors —
24%
general underdevelopment of speech (onr)
36%
8%
encephalitis —
22%
children's aphasia
26%
—
rasmussen's encephalitis —
21%
sensory alalia
23%
—
dravet syndrome —
21%
stuttering in speech
22%
—
epilepsy attacks —
21%
sensorimotor alalia
22%
—
epileptic encephalopathy in children —
20%
phonetic and phonemic underdevelopment (ffn)
21%
—
cysticercosis —
20%
agrammatism
21%
—
stroke —
20%
speech absence
20%
—
encephalopathy —
20%
psychologist
20%
—
angelman syndrome —
20%
stuttering
20%
—
apoplexy —
19%
onr 4 levels
20%
—
panagiotopoulos syndrome —
19%
level 2 onr
20%
—
twitching of the body —
19%
onr 3 levels
20%
—
hemorrhagic stroke —
19%
chanted speech
19%
—
small epileptic seizure —
19%
hospitalism in children
18%
—
focal cortical dysplasia —
19%
impaired understanding of speech
16%
—
tiki in children —
19%
asphyxia of newborns
16%
—
temporal lobe epilepsy —
19%
level 1 onr
16%
—
febrile convulsions in children —
18%
talks about death
16%
—
epilepsy in pregnant women —
18%
dysarthria in children
16%
—
twitching of the hands —
18%
not enough communication
16%
—
twitching of the head —
18%
says the same
22%
6%
childhood absentee epilepsy —
18%
paraphasia
14%
—
juvenile absentee epilepsy —
18%
conflict with the mother
14%
—
epileptic psychosis —
18%
rhinolalia
14%
—
neonatal convulsions —
18%
fetal hypoxia
14%
—
cramps of the hands —
18%
slowness of movement
14%
—
paresis
5%
23%
umbilical
14%
—
epilepsy
6%
24%
deaf and dumb
14%
—
tuberous sclerosis —
17%
emotional child
13%
—
brain development abnormalities —
17%
left hemisphere dysfunction
13%
—
lennox-gastaut syndrome —
17%
stuttering in childhood
13%
—
happy —
17%
lambdacism
13%
—
aura —
17%
replacing sounds
12%
—
vascular tumor —
17%
hyperactive
12%
—
bouts of vision loss —
17%
birth trauma of the head
12%
—
kidney diseases —
17%
cytomegalovirus infection in pregnant women
12%
—
nocturnal epilepsy attacks —
17%
dysprosody
12%
—
spasm —
17%
cytomegalovirus infection in children
12%
—
epilepsy in a dream —
17%
toxoplasmosis during pregnancy
12%
—
ischemic stroke —
17%
Alexia
12%
—
cramp and spasm —
17%
dysarthria
20%
6%
myoclonic epilepsy —
17%
conflict in the family
11%
—
lipid metabolism —
17%
delayed stages of development
11%
—
pregnancy
16%
33%
sigmatism
11%
—
muscle weakness
5%
22%
dyslalia
11%
—
learning difficulties —
16%
mom has diabetes
11%
—
perinatal encephalopathy —
16%
speech slurred
25%
12%
postencephalitic syndrome —
16%
toxicosis of pregnancy in mom
11%
—
epilepsy at night —
16%
rapid childbirth
11%
—
cysticercosis of the brain —
16%
assiduous
11%
—
tonic-clonic convulsions —
16%
rubella during pregnancy
11%
—
cerebral palsy —
16%
limited vocabulary
11%
—
boring guy —
16%
premature birth
18%
6%
hippocampus is not symmetrical —
16%
hypoxia during childbirth
10%
—
convulsions in sleep —
16%
head injury in anamnesis
10%
—
kozhevnikovskaya epilepsy —
16%
up strong
10%
—
focal epilepsy —
16%
aggressive behavior of children
10%
—
epilepsy in the morning —
16%
preeclampsia
10%
—
viral encephalitis —
16%
intranatal death
10%
—
liver problems —
16%
misunderstanding
9%
—
periodic weakness —
16%
stuttering in children
9%
—
diabetic encephalopathy —
15%
operative delivery
9%
—
arm and leg cramps —
15%
rickets
9%
—
hydrocephalus —
15%
fidgety
9%
—
generalized epilepsy —
15%
number of births has been reduced
9%
—
mitochondrial myopathy —
15%
familial diabetes
9%
—
consequences of head injury —
15%
miscarriage
9%
—
sudden onset —
15%
child is not says
9%
—
clonic cramps —
15%
confuses the words
8%
—
convulsions in the anamnesis —
15%
fine motor skills are impaired
8%
—
look absent —
15%
hypotrophy
8%
—
biotinidase deficiency —
15%
myoclonic dystonia
8%
—
glioma —
15%
paresis of the foot
8%
—
tonic convulsions —
15%
urolithiasis in children
8%
—
connective tissue dysplasia —
15%
rapid speech
8%
—
cramps at night —
15%
consumes alcohol
8%
—
a history of neurosurgery —
14%
errors in speech
8%
—
arteriovenous malformation —
14%
diseases of infants
8%
—
thrombosis —
14%
oncology in the anamnesis
8%
—
apnea —
14%
stims
8%
—
hyperventilation —
14%
needs understanding
8%
—
impulsiveness —
14%
demyelinating diseases
8%
—
periodic paralysis —
14%
micrognathia
8%
—
memory loss —
14%
lower paraparesis
8%
—
lack of sleep —
14%
thin
19%
9%
intellectual disabilities in children —
14%
hemolytic disease of newborns
8%
—
disorders of cerebrospinal circulation —
14%
moral
8%
—
muscle hypertonus —
14%
ataxia
18%
8%
pork tapeworm —
14%
suffocation
18%
8%
absences —
14%
rhesus conflict
8%
—
tick-borne encephalitis —
14%
stigmas of dysembriogenesis
8%
—
porphyria —
14%
impaired coordination
19%
9%
anxiety attack —
14%
tooth mobility
8%
—
convulsive syndrome in children —
14%