Understanding and recognizing risk factors and clinical
clues for communication disorders is an important way to identify children
under the age of 3 with possible communication disorders. Some of these risk
factors and clinical clues can be identified at a very early age; others are
not as apparent and may not be recognized until caregivers or professionals
notice that the child's use of language is delayed. In general, risk factors
for communication disorders that can be identified early in infancy are those
that are closely related to certain biological and social-environmental
factors.
The presence of a particular risk factor or clinical clue is
not sufficient to establish that a communication disorder exists. Risk factors
and clinical clues for communication disorders are sometimes seen in children
who are typically developing and do not have a communication disorder.
Therefore, recognition of a risk factor or clinical clue is just the first step
in the process of identifying children with communication disorders and merely
indicates that further assessment is needed.
Table-1:
Risk Factors for Speech / Language Problems In Young
Children
Prenatal complications
Prematurity*
Microcephaly
Dysmorphic child features
Genetic disorders
Fetal alcohol syndrome
Known exposure to a teratogen
Positive toxicology screen at birth
Ear and hearing problems (See Table III-2)
Oral-motor or feeding problems (See Table III-3)
Cleft lip/cleft palate
Tracheotomy
Autism (See Table III-4)
Persistent health/medical problems, chronic illness, or
prolonged hospitalization
History of intubation
Lead poisoning
Failure to thrive
Family history of hearing or speech/language problems
Parents with hearing impairment or cognitive limitation
Children in foster care
Family history of child maltreatment (physical abuse or
child neglect)
* The more premature the birth and the more complicated the
perinatal course, the greater the risk is for communication disorders and other
developmental problems.
Table-2:
Risk Factors for Hearing Problems in Young Children
Family history of hereditary childhood sensorineural hearing
loss
Congenital infections known to be associated with hearing
loss
Craniofacial anomalies
Birth weight less than 1,500 grams
A genetic syndrome known to include hearing loss
Low Apgar Scores (0-4 at one minute or 0-6 at five minutes)
Hyperbilirubinemia requiring exchange transfusion
Ototoxic medications
Bacterial meningitis
Mechanical ventilation for five days or longer
Recurrent or chronic otitis media with effusion
From: Joint Committee on Infant Hearing, 1994
Table -3:
Risk Factors And Clinical Clues For Oral-motor/Feeding
Problems in Young Children
Craniofacial disorders or syndromes (of the head and neck)
Cleft lip/cleft palate
Tracheotomy
Cerebral palsy
Poor weight gain
Prolonged feeding time
Poor suck
Gagging
Excessive drooling
Hyper/hypo sensitivity
Undifferentiated cry sounds
Poor volume or quality of crying
Lack of reciprocal babbling
Reduced vocal play
Failure to thrive
Table-4
Clinical Clues of Possible Autism in Young Children
The clinical clues listed below represent delayed or
atypical behaviors that are seen in children with autism (although some of
these findings may also be seen in children who have a developmental delay or
disorder other than autism).
If any of these clinical clues are present, further
assessment may be needed to evaluate the possibility of autism or other
developmental disorder.
Delay or absence of spoken language
Looks through people; not aware of others
Not responsive to other peoples facial expressions/feelings
Lack of pretend play; little or no imagination
Does not show typical interest in, or play near peers
purposefully
Lack of turn taking
Unable to share pleasure
Qualitative impairment in nonverbal communication
Does not point at an object to direct another person to look
at it
Lack of gaze monitoring
Lack of initiation of activity or social play
Unusual or repetitive hand and finger mannerisms
Unusual reactions, or lack of reaction, to sensory stimuli
From: Clinical Practice Guideline for Autism/Pervasive
Developmental Disorder, New York State Department of Health, 1999.
No comments:
Post a Comment