Pediatric Syndromal Hearing Loss
Transcript of Pediatric Syndromal Hearing Loss
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Pediatric Syndromal
Hearing Loss
Ryan Ridley, MD
Shraddha
Mukerji, MD
University of Texas Medical Branch
Department of Otolaryngology Grand Rounds Presentation
September 24, 2009
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OUTLINE
•
Introduction
•
Basic Mendelian Genetics
•
Approach to the syndromic
child
•
Specific syndromes
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1/1,000 Born Deaf
50% Hereditary-genetic 50% acquired prenatally½
idiopathicIntrauterine infection (TORCHS)Low birth weightHypoxiaHyperbilirubinemiaNon-genetic syndromes
Goldenhar’sFAS
1/3 syndromic 2/3 nonsyndromic
DominantWaardenburgBORStickler’sNF2Treacher
CollinsRecessive
UsherPendredJervell/Lange-Nielsen
X-linkedAlport
23% dominant75% recessive2% X-linked1% mitochondrial
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Approach to the Syndromal
Patient
•
Family History–
Is there a FHx
reported?
–
Associated clinical
features in the family?
–
Do not assume parents
hear normally•
Eval
parents’
hearing
–
Inquire about hearing of
other family members
–
Consanguinity?
•
Birth/developmental Hx–
Rubella status of mother
–
Motor delay
–
Global developmental
delay
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Approach to the Syndromal
Patient
Physical exam
•
External ears (size, shape)
•
Eyes (color, spacing, etc)
•
Neck (cyst , fistulas, length)
•
Pigmentation
•
Hands/feet/fingers/toes
•
How does child look at first
glance?–
Dysmorphic
or is this a family
trait?
•
Facial asymmetry
Investigations
•
Audiogram of 1st‐degree
relatives
•
Ophthalmology exam
•
Serologies
(TORCH)
•
Urinalysis
•
EKG
•
Chromosome analysis
•
CT temporal bone
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Autosomal
Dominant Syndromes
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Waardenburg
Syndrome
•
Epidemiology–
1 in 20,000 to 1 in 40,000
–
3% of congenitally deaf children
•
Etiology–
PAX3
mutation (type 1 and 3)
–
MITF
mutation (type 2)
–
EDNRB
mutation (type 4)
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Waardenburg
Syndrome
•
General clinical characteristics
–
Dystopia canthorum
–
Pinched nose
–
Heterochromia
iridis
–
Abnormal pigmentation
of skin and hair
–
Broad nasal bridge and
hypoplastic
alae
nasi
–
High arched or cleft
palate
http://dermatology.cdlib.org/123/case_presentations/waardenburg/1.jpg
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Waardenburg
Syndrome
Otologic
characteristics
•
Hypoplastic
ear cartilage
•
Abnormal vestibular
function (type 2)
•
SNHL –
Bilateral most common
–
Low‐mid frequency loss
–
CI can be expected to yield
improved speech perception
and speech intelligibility
capabilities •
Daneshi, et al. J Laryngol
Otol. 2005
4 subtypes
•
Type 1: every patient
exhibits dystopia
canthorum
•
Type 2: void of dystopia
canthorum, but vestibular
abnormalities present
•
Type 3: Type 1 + upper
extremity abnormalities +
unilateral upper lid ptosis
•
Type 4: Type 2 +
pigmentation abnormalities
+ Hirschsprung
disease
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Branchio‐Oto‐Renal
Syndrome
•
Epidemiology–
2% of profoundly deaf children
•
Etiology–
EYA1 gene mutation
–
High penetrance, variable expressivity
•
Diagnosis–
At least 3 major criteria
–
Two major criteria and at least two minor criteria
–
One major criteria with one first‐
degree relative meeting BOR criteria
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Branchio‐Oto‐Renal
Syndrome
•
Hearing impairment–
estimated to be present
in 70‐93%
–
Variable age of onset
–
Mild to profound
severity
–
SNHL, CHL, or mixed
–
Mondini’s
dysplasia and
stapes fixation can also
be present
•
Other characteristics–
cup‐shaped pinnae,
–
preauricular
pits/tags
–
Lacrimal
duct stenosis
–
branchial
cleft fistulae
–
bilateral renal
anomalies.
–
deep overbite and a
long , narrow face
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Branchio‐Oto‐Renal
Syndrome
Kochhar, et al. 2007
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Stickler Syndrome
General characteristics
• Progressive SNHL
• Cleft palate,
•
abnormal development of
the epiphysis,
•
vertebral abnormalities/
osteoarthritis.
•
Genetics–
COL2A1, COL11A1, and
COL11A2 mutations
Subtypes
•
Type 1 –
progressive myopathy,
–
retinal detachment
–
Vitreoretinal
degeneration
•
Type 2: –
no retinal detachment
•
Type 3 –
eye and ear findings present
in type 1 but has facial
abnormalities
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Treacher
Collins Syndrome (TC)
•
Fraceschetti‐Zwahlen‐Klein
Syndrome or Mandibulo‐Facial Dysostosis
•
Etiology–
TCOF gene mutation on 5q32‐q33.1
•
Typical features–
microtia
and malformed ears
–
midface
hypoplasia
–
micrognathia
–
downslanting
palpebral
fissures
–
coloboma
of outer 1/3 of lower eyelids.
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•
Airway–
Upper airway narrowing
a major issue
–
Nasopharynx
50%
smaller than normal
–
More prone to OSA and
SIDS
•
Ears/Hearing–
Usually CHL
•
Absent/stenotic
EAC
•
Middle ear anomalies–
as monopodal
stapes
–
ankylosed
foot plate
–
malformed incus
–
cochlea and vestibule
abnormalities
–
SNHL•
Affects high frequencies
Treacher
Collins Syndrome (TC)
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Treacher
Collins Syndrome (TC)
www.craniofacial.net/treacher_collins_syndrom...
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Neurofibromatosis Type 2 (NF2)
•
Epidemiology–
Prevalence of 1 in 210,000 people
•
Etiology–
NF 2 tumor suppressor gene mutation on
chromosome 22
•
Diagnosis–
Manchester criteria
–
Audiometry–
MRI with gadolinium
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NF 2 Clinical Features•
Meningiomas•
Ependymomas•
Gliomas•
Lens opacities•
Café‐au‐lait
spots (few)•
Cranial nerve, spinal and
peripheral nerve schwannomas
•
Otologic
–
Bilateral vestibular
schwannomas
–
Tinnitus, disequilibrium, cranial
nerve symptoms
–
Usually present in 2nd
and 4th
decade
–
Many present with unilateral
SNHL instead of bilateral SNHL
–
Children < 15 yo
often present
w/o HL or schwanoma
development
–
Rehab
•
Hearing aids for moderate
HL
•
Success with CI s/p
tumor
removal
–
Neff and Welling, Otowww.yvonnefoong.com/image/an.jpg
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Osteogenesis
Imperfecta
(OI)
•
Triad–
Bone fragility
–
Blue sclera–
Hearing impairment
•
Incidence–
1 in 20,000‐
1 in 30,000
•
Etiology–
Mutation in COL1A1 or
COL1A2–
Type I collagen defect
www.gfmer.ch/.../gendis_detail_list.php?cat3=742
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OI Clinical Characteristics
•
Hypermobile
joints•
Short stature
•
Triangular face•
Cardiovascular
abnormalities•
Skin disorders
•
Hearing Impairment–
Usually presents in 2nd or
3rd
decade–
Mixed (prevalence 26‐78%)
•
CHL due to thickened, fixed
stapes footplate
•
SNHL–
cochlear hair cell atrophy–
Atrophy of stria
vascularis
–
Bony formation around
cochlea
–
Stapedotomy
may
facilitate hearing aid rehab
•
Swinnen
et al., 2009
Laryngoscope
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Osteogenesis
Imperfecta
Otospongiosiswww.gfmer.ch/.../gendis_detail_list.php?cat3=742
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Autosomal
Recessive Syndromes
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Usher Syndrome
•
Epidemiology–
Most common autosomal
recessive cause of HL
–
incidence ~ 3‐5 per 100,000 in the general population
–
1‐10% among profoundly deaf children
–
Approximately 50% of blind and deaf in US
•
Etiology–
USH1 and USH2 gene mutations
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Usher Syndrome
•
3 Main subtypes
•
Type 1–
severe hearing loss and vestibular dysfunction.
–
onset of retinitis pigmentosa
in childhood
•
Type 2 –
Retinitis pigmentosa
begins after childhood.
–
Mild to moderate hearing loss
–
Normal vestibular function.
•
Type 3, –
Progressive hearing loss & vestibular dysfunction.
–
Retinitis pigmentosa
can occur anytime in life.
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Pendred
Syndrome
•
Characterized by hearing impairment & abnormal iodine metabolism.
•
Etiology/Pathogenesis–
SLC26A4 (PDS) gene mutation
–
Encodes protein which helps regulate iodine and chloride ion transport
•
Characteristics–
Euthyroid
goiter
•
Diagnose with thyroid function tests
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Pendred
Syndrome
•
Hearing
– Severe SNHL
•
present at birth or progressive
– Inner ear abnormalities
•
Mondini’s
•
EVAJournal of Clinical Endocrinology & Metabolism
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Jervell
and Lange‐Nielsen Syndrome
•
Incidence: –
1.6‐6 cases per million in certain parts of Europe
–
6 per 1,000 in congenitally deaf children
•
Characterized by severe‐profound hearing loss
and prolongation of the QT interval on EKG–
syncopal
episodes due to cardiac conduction
defect •
Can manifest as early as the 2nd
or 3rd
year of life
•
Should suspect in a child with hearing loss and seizures
of unknown origin and/or a family history of sudden
death
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•
Etiology–
Cardiac conduction defects attributed to
mutations in potassium channel genes•
loci on the KVLQT1 and KCNE1 genes located on
chromosomes 11p15.5 and
21q22 respectively.
•
Hearing rehabilitation with cochlear implant–
Comparable auditory and speech outcomes
compared to nonsyndromic
patients with SNHL •
Yanmei
et al. In J Pediatr
Otorhinolaryngol
2008
Jervell
and Lange‐Nielsen Syndrome
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Biotinidase
Deficiency•
Features–
Rashes
–
Seizures
–
Hair loss
–
Hypotonia
–
Emesis & acidosis
–
Hearing loss•
75% occurrence if left
untreated
•
Etiology–
lacks of enzyme
responsible for proper
biotin metabolism
Before biotin
After biotin
www.vanwaverenmarken.com/bioti.htm
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X‐linked Syndromes
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Alport
Syndrome
Features
•
Eye–
Congenital cataracts
•
Renal–
Glomerulonephritis
–
Hematuria
–
Renal failure
•
Ear–
Bilateral progressive SNHL
–
Onset in 2nd
decade
Etiology
•
mutation in type IV collagen
gene COL4A5
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Infectious Syndromes
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Cytomegalovirus (CMV)
•
Epidemiology–
Incidence of 0.2‐2.3% of live births
–
One of the most frequently occuring
viruses
–
Leading cause of congenital malformation and mental retardation
–
Most prevalent TORCH infection
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CMV Common Clinical Characteristics
•
Microcephaly•
IUGR*
•
Petechiae*•
Hepatosplenomegaly
•
Encephalitis
*2‐3 times more likely to have
SNHL
•
Deafness–
1/3 of SNHL in young children–
May be delayed–
Can be fluctuating and
progressive
–
Temporal bone studies•
CMV inclusion bodies in stria
vascularis, saccule
utricle, SCC,
Reissner’s
membrane.•
Endolymphatic
hydrops
in
cochlear ducts
–
Stabilization or improvement
of hearing with antiviral tx
of
symptomatic neonates.
•
Dahle
et al, J Am Acad
Audiol
2000
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CMV
www.thesahara.info/mrsa/mrsa_cytomegalovirus.jpg
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Congenital Rubella
•
Classic triad–
Deafness
–
Congenital cataracts–
Heart defects
•
Etiology–
RNA togavirus
•
Transmission–
Congenital and postnatal transmission possible
•
Congenital‐
transplacental
•
Postnatal‐
saliva, sputum, direct contact
www.idph.state.il.us/images/rubella.jpg
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•
Diagnosis–
Positive viral culture
–
Rubella specific IgM
antibody
–
Significant rise in IgG
antibody in acute and convalescent phase
Congenital Rubella
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Congenital Rubella: Clinical
•
Microcephaly
•
Thrombocytopenia
•
Hepatosplenomegally
•
Motor/neural retardation
•
Encephalitis
•
Interstitial pneumonitis
•
Hearing loss–
Asymmetric, SNHL
•
Variable severity
•
May be progressive
•
Usually 500‐2000Hz
•
Usually evident by 5 yo–
May be isolated finding
–
Bento et al. , 2005•
~30% of infants born to
rubella infected mothers
had SNHL–
80% were profound
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Rubella congenital cataracts
www.vaccineinformation.org/photos/rubeiac003a.jpg
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Non‐Genetic Syndromes
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Goldenhar’s
Syndrome
•
Aka hemifacial microsomia
(HFM),
facioauriculovertebral dysplasia (FAVD)
•
Incidence: 1 in 5600 live births
–
Most significant
asymmetric craniofacial
disorder
www.i‐am‐pregnant.com/.../Goldenhar‐Syndrome.jpg
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Goldenhar’s
Syndrome
Facial anomalies (unilateral)•
Hypoplasia
of mandible
–
Ramus
and condyle
•
Hypoplasia
of maxilla, malar
and temporal bones
•
Macrostomia
and
pseudomacrostomia
•
Cleft lip/palate
•
Delayed dental
development
Otologic
abnormalities
•
microtia/anotia
•
preauricular
tags
•
ossicular
abnormalities
• abnormal facial nerve
course
•
hearing loss (conductive >
sensorineural).–
HL secondary to abnormal
development of 1st
and 2nd
arch structures
www.earreconstruction.co.uk/fig‐microtia/Pair
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Goldenhar’s: Non‐Head & Neck Manifestations
•
Cardiac–
COA
–
VSD–
TOF
–
PDA
•
Renal–
Hydronephrosis
–
Renal ectopia
•
Musculoskeletal–
Limb deformities
•
Ocular–
blepharoptosis
–
Microopthalmia–
epibulbar
tumors
–
retinal abnormalities
leading to reduced visual
acuity.
www.ophthalmic.hyperguides.com/.../slide5.jpg
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Fetal Alcohol Syndrome (FAS)
•
Epidemiology–
Occurs in 30‐40% of children born to alcoholic
mothers
•
Etiology/Pathogenesis–
Exact amount of alcohol required unknown
–
Teratogenic
restriction of cell growth during critical periods
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•
Neural tube defects•
Seizure disorder
•
Microopthalmia•
Optic nerve hypoplasia
•
Tortuous retinal vessels•
Colobomas
•
Malignant neoplasms
of embryonal
origin
•
Deafness–
SNHL or CHL
•
Pre/Postnatal growth defeciency
•
Behavioral–
Mental retardation; IQ=63
–
Irritability & hyperactivity
•
Cardiac, renal, musculoskeletal
abnormalities
FAS Characteristics
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Facial Dysmorphisms
Narrow forehead
Short palpebral
fissures
Ptotic
eyelids
Midface
hypoplasia
Short nose
Smooth philthrum
Thin upper lip
Hypoplastic
mandible
Cleft palate/lip
www
nlm
nih
gov/
/ency/fullsize/21723
jpg
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Down’s Syndrome
•
Epidemiology: –
Most common syndrome caused by chromosome
abnormality
•
Etiology–
Trisomy
of chromosome 21
www.thespeciallife.com/image‐files/downs‐synd...
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Down’s: Clinical Features
•
Cardiovascular–
VSD, TOF, PDA,
•
Genitourinary–
Small penis, low
testosterone, infertility
•
Musculoskeletal–
Atlantoaxial
instability,
short digits
•
Ocular–
Brushfield
spots
•
Behavioral/Psych–
IQ=30‐50
medgen.genetics.utah.edu/.../high/peri003.jpg
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Down’s: Clinical Otolaryngologic
•
Ears–
Small ears, stenotic
EAC, ETD
–
Increased incidence of OM•
ETD
•
Increased propensity for URI
•
Reduced B and T cell function (immune system immaturity)
–
Hearing loss (CHL, SNHL, or mixed)•
OM
•
Middle ear abnormalities (stapes)
•
May suffer presbycusis
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•
Airway–
Upper airway obstruction and OSA
•
Midface
hypoplasia
•
Relative macroglossia
•
Relatively enlarged tonsils and adenoids
•
Speech–
Articulation defects/ dysarthria
Down’s: Clinical Otolaryngologic
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Closing Thought
•
The method of treatment should be selected to meet the individual needs of the patient to achieve the most benefit.
•
The main purpose of arriving at a syndromic diagnosis is to identify those that will have
hearing loss so that early and aggressive hearing rehabilitation can be initialized.
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Real life scenario
•
www.usherssyndromefoundation.org
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Bibiolography
Hearing, speech, language, and vestibular disorders in the fetal alcohol syndrome: a literature review. Church MW, Kaltenbach JA. Alcohol Clin Exp Res. 1997 May;21(3):495-512. Review
Hearing, language, speech, vestibular, and dentofacial disorders in fetal alcohol syndrome. Church MW, Eldis F, Blakley BW, Bawle EV. Alcohol Clin Exp Res. 1997 Apr;21(2):227-37
Treatment of otological features of the oculoauriculovertebral dysplasia (Goldenhar syndrome). Skarzyński H, Porowski M, Podskarbi-Fayette R. Int J Pediatr Otorhinolaryngol. 2009 Jul;73(7):915-21. Epub 2009 Feb 8
Goldenhar's syndrome: congenital hearing deficit of conductive or sensorineural origin? Temporal bone histopathologic study. Scholtz AW, Fish JH 3rd, Kammen-Jolly K, Ichiki H, Hussl B, Kreczy A, Schrott-Fischer A. Otol Neurotol. 2001 Jul;22(4):501-5
An overview of hereditary hearing loss. Bayazit YA, Yilmaz M. ORL J Otorhinolaryngol Relat Spec. 2006;68(2):57-63. Epub 2006 Jan 20. Review.
Branchio-oto-renal syndrome. Kochhar A, Fischer SM, Kimberling WJ, Smith RJ. Am J Med Genet A. 2007 Jul 15;143A(14):1671-8. Review
Current concepts in the evaluation and treatment of neurofibromatosis type II. Neff BA, Welling DB. Otolaryngol Clin North Am. 2005 Aug;38(4):671-84, ix. Review
Cochlear implantation in individuals with Usher type 1 syndrome. Liu XZ, Angeli SI, Rajput K, Yan D, Hodges AV, Eshraghi A, Telischi FF, Balkany TJ. Int J Pediatr Otorhinolaryngol. 2008 Jun;72(6):841-7. Epub 2008 Apr 18
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Cochlear implantation in patients with Jervell and Lange-Nielsen syndrome, and a review of literature. Yanmei F, Yaqin W, Haibo S, Huiqun Z, Zhengnong C, Dongzhen Y, Shankai Y.Int J Pediatr Otorhinolaryngol. 2008 Nov;72(11):1723-9. Epub 2008 Sep 20. Review.
Otopathology in Mohr-Tranebjaerg syndrome. Bahmad F Jr, Merchant SN, Nadol JB Jr, Tranebjaerg L. Laryngoscope. 2007 Jul;117(7):1202-8.
The ABCs of CMV. DeVries J. Adv Neonatal Care. 2007 Oct;7(5):248-55; quiz 256-7. Review
Role of cytomegalovirus in sensorineural hearing loss of children: a case-control study Tehran, Iran. Samileh N, Ahmad S, Mohammad F, Framarz M, Azardokht T, Jomeht E. Int J Pediatr Otorhinolaryngol. 2008 Feb;72(2):203-8. Epub 2007 Dec 4.
Audiometric, surgical, and genetic findings in 15 ears of patients with osteogenesis imperfecta. Swinnen FK, De Leenheer EM, Coucke PJ, Cremers CW, Dhooge IJ. Laryngoscope. 2009 Jun;119(6):1171-9.
Down syndrome: common otolaryngologic manifestations. Shott SR. Am J Med Genet C Semin Med Genet. 2006 Aug 15;142C(3):131-40. Review
Auditory brainstem response and otoacoustic emission assessment of hearing-impaired children of mothers who contracted rubella during pregnancy. Bento RF, Castilho AM, Sakae FA, Andrade JQ, Zugaib M. Acta Otolaryngol. 2005 May;125(5):492-4.
Bailey, Byron J.; Head & Neck Surgery - Otolaryngology 4th Edition