Tuesday, July 24, 2012


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