Caution! This text is rather medical. If you don't understand
something, never minds - me too.
CHARGE Association (or Syndrome) is an acronym
specifying children with specific configuration of defects when they are born.
Acronym is composed of: "C" - coloboma, "H" - heart defects; "a"
- atresia choanae (stenosis); "R" - retardation of growth and/or
developmental delay; "G" - genitourinary problems; "E" -
ear abnormalities.
This type of characteristics was first described by Hall in 1979
[1], but acronym 'CHARGE' was used first in 1981
[2].
C = Coloboma
a coloboma is a cleft or failure to close of the eyeball. This can result in a
keyhole shaped pupil and/or abnormalities in the retina or optic nerve.
Colobomas of the retina or optic nerve may result in significant vision loss,
especially visual field defects in the upper half of the visual field. Visual
acuity may also be affected, resulting in nearsightedness or farsightedness.
Surgery cannot correct ocular colobomas, but glasses often help with visual
acuity. Children with CHARGE Syndrome are often very sensitive to light. Many
are more comfortable with sunglasses, even indoors.
Sometimes the eyes may be small.
These problems may cause a
range of difficulties which include blindness, low vision, loss of visual
field, a need to wear glasses, difficulty coping with bright light, and
sometimes a risk of further eye problems such as retinal detachment.
C = Cranial nerves
About 40% of children with
CHARGE Syndrome have facial palsy (cranial nerve VII), and at least 30% have
swallowing problems (cranial nerve IX/X). Children with facial palsy may be
more likely to have sensorineural hearing loss (cranial nerve VIII). Swallowing
problems often last for years, but typically resolve by age 7 or 8 years.
H = Heart
Heart defects may be of various kinds.
About 80% of children with CHARGE Syndrome are born with a heart defect. Many
are minor defects, but many require treatment or surgery. Some of the complex
heart defects seen in CHARGE Syndrome (e.g. Tetralogy of Fallot) can be life
threatening.
a = Atresia of the choanae
The choanae are the passages from the back of the nose to the throat which
make it possible to breathe through the nose. In children with CHARGE Syndrome,
these passages may be blocked (atresia) or narrowed (stenosis). Surgery can
often correct these defects. Multiple surgeries are often required.
R = Retardation of growth and/or development
Although most children with CHARGE Syndrome are average size at birth, many
will become small due to nutrition problems, heart problems, or growth hormone
deficiency. Some catch up after the severe medical problems and feeding
problems have resolved.
Most children with CHARGE Syndrome will be developmentally delayed. Often,
this is primarily due to sensory deficits (vision loss and/or hearing loss) and
frequent hospitalizations as infants. Some children with CHARGE Syndrome will
be mentally retarded, with or without brain abnormalities.
Historically, the medical profession considered mental retardation a
characteristic feature of CHARGE Association. Recent literature suggests this
may now be coming to be seen as an outcome of the other combined anomalies
rather than as an integral anomaly of the Association itself. [3] [4] Evidence
from families and involved professionals suggests that people with CHARGE
Association cover the whole spectrum of intellectual ability from severe
retardation through to normal or even high intelligence.
Retarded growth and development may become evident as the child matures; most
of the people identified as having CHARGE Association are below the third
percentile of physical growth norms. There are multiple factors leading to
retarded growth including severe feeding difficulties, reflux, breathing
problems, chest infections, and multiple surgical procedures with repeated and
prolonged hospitalisation.
G = Genital and urinary abnormalities
Many boys with CHARGE Syndrome have a small penis and/or undescended testes.
Girls may have small labia. Boys or girls with CHARGE Syndrome may require
hormone therapy to achieve puberty. Boys and girls may have kidney or urinary
tract abnormalities, especially reflux.
E = Ear abnormalities and hearing loss
Most children with CHARGE Syndrome have unusual external ears, including
short, wide ears with little or no earlobe, often with a "snipped off"
appearance to the helix (outer fold of the ear). The ears may be soft due to
floppy cartilage. Keeping a hearing aid in place is often difficult.
Hearing loss (conductive and/or nerve) is present in 80 - 85% of children with
CHARGE Syndrome, ranging from mild hearing loss to profound deafness. The
hearing loss can be difficult to evaluate due to frequent ear infections,
presence of other medical conditions, and general difficulty of testing. Many
children have additional conductive losses due to frequent ear infections. Many
children also have difficulty with balance.
middle ear (bone malformations or chronic glue-ear infections), The most
common form of hearing loss found in people with CHARGE Association is mixed
i.e. a conductive loss because of middle-ear problems combined with a
sensori-neural loss because of problems with the cochlea.
Children with CHARGE Syndrome may have other birth defects, including
- Poor immune response.
- Some children are difficult to sedate for testing.
- There may
be some behavior problems associated with CHARGE Syndrome, but not enough
information is available at this time.
- Malformed or absent semi-circular canals which means that the balance sense
will be affected or absent.
- Before
they can walk, children with CHARGE often move by lying flat on their backs and
scooting headfirst or by five-point crawting (i.e. two arms, two legs and
forehead) backwards or forwards.
- Once
walking, people with CHARGE often show the characteristic pattern of feet
rather wide apart, knees slightly bent. feet being planted firmly on the ground
and the upper body and head slightly rolling from side to side. This
characteristic gait is thought to result from a combination of balance
problems, visual impairment, and poor muscle tone.
- Facial
Palsy: This is a type of paralysis that can leave the face looking flat and
expressionless. The facial nerve that suppiles the facial muscles does not work
properly. This usually affects just one side of the face. This distinctive
feature may become more or less apparent in people with CHARGE as they grow and
develop. It has implications for communication because of the way that facial
expressions and speech may be affected.
- Immune
System Deficiency: This is seen in children who show an overlap with DiGeorge
Sequence. They have an increased risk of infection.
- Larynx/Pharynx
Problems: Children with facial palsy are more likely to have structural
anomalies in the region of the larynx and pharynx. Ths may lead to swallowing
problems and aspiration of food andlor saliva.
- Micrognathia:
This means a small lower jaw that may contribute to feeding difficulties, and
may be another factor to consider in the development of speech.
- Sensory
Defensiveness: Difficulties in coping with stimulation from environments that
are quite normal and not at all over-stimulating seem to be a feature of many
people with CHARGE. It is likely that people with CHARGE encounter difficulties
with all their senses.
- Sleep
Apnoea: Disturbed sleep patterns due to periods of arrested breathing are
coming to be seen as a feature of infants with CHARGE.
- Swallowing
Abnormalities: Some problems with co-ordinating breathing and swallowing can be
attributed to damage to the ninth and tenth cranial nerves. Additional
contributory factors may be breathing difficulties, hypotonia, weak or
malformed oesophagus and trachea, and sensory defensiveness.
Causes
CHARGE Association is usually sporadic with no other affected individuals in
the family. There are rare reports of multiple affected individuals in a
family. Recurrence risk is low, probably 1-2%. The risk of an affected
individual having an affected child may be much higher.
The exact cause of CHARGE Association is still unknown and research suggests a
variety of factors which may induce the irregularities which are present in
this condition. The majority of cases are thought to be sporadic with no
obvious evidence of genetic involvement. There is some evidence in the
literature of cases where certain characteristics of CHARGE have been
inherited, and also some evidence to suggest chromosome deletion in some cases.
Reference in the literature, and many parents of people with CHARGE
Association, suggest the possibility of linking CHARGE with exposure to certain
chemicals (pesticides, fungicides, and wood preservatives) but this has not
been proven.
Affected Population
The incidence of CHARGE is about 1/10,000-1/12,000 births. It is probably very
underdiagnosed. The frequency is the same in males and females. CHARGE has been
seen in all races.
Prognosis
Choanal atresia is life-threatening because young infants cannot establish the
habit of breathing through their mouths. Prognosis is based on the severity of
factors. For example, a severe case with major developmental delay and growth
retardation has a poor prognosis while one with surgically correctable
malformations may lead a happy, healthy life.
Very little is known about the life expectancy of people with CHARGE
Association, nor about the likelihood or nature of late onset complications.
One difficulty is that this is a comparatively recently identified condition;
if people were born with CHARGE Association well before 1982 it is unlikely
that they will be identified as having the condition in their adult years.
Another possible explanation is that babies born with CHARGE Association
generally died because medical science was unable to support them through the
first immensely complex and difficult years of life; nowadays we have the
technology to achieve this in most cases.
Although these children have many problems, they can survive and become healthy,
happy citizens. Many of the structural abnormalities (choanal atresia, heart
defects, cleft lip, etc.) can be surgically corrected. In any child in whom
CHARGE is suspected, complete cardiac (heart), ophthalmological (eye), and
audiological (hearing) evaluations should be performed, as well as abdominal
ultrasound (kidney), and chromosome evaluation.
Appropriate therapies and educational intervention must take into account any
hearing and vision loss which is present. The intelligence of children with
CHARGE is often underestimated due to the combined hearing and vision problems.
Management should be by a multidisciplinary team and coordinated by a single
person, if possible.
Most of the literature on CHARGE is medical and until five or six years ago
showed little understanding of the educational needs or potential for
development of children with CHARGE Association. This has improved in more
recent literature and, as explained above, with growing awareness of the
importance of early educational intervention and of the need for appropriate
educational approaches, it should become increasingly rare for 'mental
retardation' to be automatically ascribed to young children with CHARGE
Association.
To date, no predictive factors regarding the developmental prognosis of CAS
infants have been identified. Because of their multiple complex
medical/surgical issues, many initial care providers overestimate the severity
of developmental disabilitiy in the absence of reliable data. Only by careful,
prospective follow-up of a population of CAS infants that have been ascertained
through the CPSP can their developmental profile be defined and compared to the
reported literature. The increase in paternal age of CAS children has been
recognized and needs to be further established, as does the concern with
pesticides as teratogens.
CHARGE
Syndrome Foundation, Inc.
The Wide World
of Physical Therapy, Brad Lipscomb, MS, PT,
CHARGE Family
Support Group
Literature:
[1] Hall strong. Choanal atresia and associated multiple anomalies. J Pediatr
1979;95(3):395-8.
[2] Pagon RA, Graham JM, Zonana J and Youing SL (l981). "Congenital Heart
Disease and Choanal Atresia with Multiple Anomalies" Journal of Paediatrics 99
223-227.
[3] Blake KD and Brown D (1993). "CHARGE Association Looking at the Future -
the Voice of a Family Support Group" Child: Care, Health and Development 19
395-409.
[4] Blake D, Russell-Eggitt IM, Morgan DW, Ratcliffe JM and Wyse RKH (1990).
"Who's in CHARGE? Multi-Disciplinary Management of Patients with CHARGE
Association" Archives of Diseases in Childhood 65 217-223.