Study Guide Flashcards
(88 cards)
re: non-genetic hearing loss
the TORCH complex is a set of factors that may cause hearing loss; list the factors:
(T)oxoplasmosis (O)ther bacterial infections; syphilis (R)ubella, German measles (C)ytomegalovirus, CMV (H)erpes simplex virus
re: non-genetic hearing loss
in TORCH, what is described by the following symptoms: asymptomatic adults or infants at birth; visual problems; later development of hearing loss or neurodevelopment delay
toxoplasmosis; caused by parasites in undercooked meat or cat feces; sometimes curable if present at birth
re: non-genetic hearing loss
in TORCH, what is described by the following symptoms: may cause progressive sensorineural hearing loss and vestibular dysfunction
syphilis (other bacterial infections); caused by a sexually transmitted bacterial disease transmitted in utero to fetus; treatable with antibiotics
re: non-genetic hearing loss
in TORCH, what is described by the following symptoms: may affect hearing, vision, heart development, and psychomotor development
rubella aka congenital German measles (CRS); greatest damage in first trimester; defects may present later in life
re: non-genetic hearing loss
in TORCH, what is described by the following symptoms: mostly asymptomatic; congenital neurosensory HL; 10-15% will present with progressive SNHL and / or developmental delay
cytomegalovirus; strain of herpes transmitted through contact with urine; transmitted to fetus in utero; no treatment
re: non-genetic hearing loss
in TORCH, what is described by the following symptoms: neonates show rash, organ dysfunction, neurologic difficulties, and SNHL
herpes simplex virus (HSV); fatal in 50% of cases; after parent acquires genital herpes, it is transmitted in utero to fetus
re: non-genetic hearing loss
which postnatal infection is described by the following symptoms: mild to profound bilateral SNHL which develops early in the illness; possible ossification of the cochlea
meningitis; bacteria from the meninges travel to the brain labyrinth; curable via influenza type b vaccine
re: non-genetic hearing loss
which postnatal infection is described by the following symptoms: 60% infants jaundiced or with yellow skin color; in infants, immature liver cannot handle all bodily wastes resulting in peak bilirubin levels at 3-4 days old
hyperbilirubinemia; caused by excess bilirubin neurotoxin, a byproduct of the breakdown of red blood cells
re: non-genetic hearing loss
which postnatal infection is described by the following symptoms: excessive jaundice, including yellow staining of brain nuclei, damage to cochlear nuclei in brainstem, hippocampus damage
hyperbilirubinemia; observable movement disorders, paralysis of up gaze and staining of teeth, cerebral palsy, cognitive defects, SNHL
re: non-genetic hearing loss
which postnatal infection is described by the following symptoms: damage to spiral ganglia, auditory nerve, and brainstem nuclei; associated with auditory neuropathy
hyperbilirubinemia; blood transfusions necessary in extreme cases; treated using phototherapy
re: non-genetic hearing loss
in what part of the ear do may the following anomalies occur: collapsed (narrow) ear canals; skin covered by vernix caseosa; exostoses or osteoma (bony growth); otitis externa
outer (external) ear
re: non-genetic hearing loss
what is described by the following symptoms: inflammation of the middle ear; occurs with or without effusion
otitis media
*note: middle ear
re: non-genetic hearing loss
what is described by the following symptoms: skin growing from external ear invading middle ear; growing cyst; smelly drainage, conductive HL
cholesteatoma; treated via surgery and regular monitoring
*note: middle ear
re: non-genetic hearing loss
what is described by the following symptoms: if acute, mucosa inflammation; if chronic, affected bone structure
mastoiditis; treated with antibiotics, surgery in rare cases
*note: middle ear
re: non-genetic hearing loss
what is described by the following symptoms: calcified TM scar tissue; hearing loss
tympanosclerosis; related to chronic otitis media
*note: middle ear
re: non-genetic hearing loss
what is described by the following symptoms: rapidly progressive bilaterally symmetrical SNHL
autoimmune disease
*note: inner ear
re: non-genetic hearing loss
what is described by the following symptoms: 8th nerve tumor; common in children with neurofibrosis type II
acoustic neuroma
*note: inner ear
re: non-genetic hearing loss
what is described by the following symptoms: affecting hair cells; bilateral symmetrical high-frequency SNHL
ototoxicity; caused by antibiotics, diuretics, and / or chemotherapy drugs
*note: inner ear
re: non-genetic hearing loss
what is described by the following symptoms: notches SNHL near 4000 Hz; variable susceptibility
noise-induced hearing loss
*note: inner ear
re: congenital inner ear malformation
what is described by the following symptoms: complete absence of the inner ear and auditory nerve
michel aplasia
re: congenital inner ear malformation
what is described by the following symptoms: incomplete development of the membranous and bony labyrinth
mordini aplasia
re: postnatal stages of auditory development
describe stage I: maturation of neural encoding of fundamental characteristics of sound
less than 6 months; immature frequency discrimination, resolution, selectivity, specificity
re: postnatal stages of auditory development
describe stage II: increased specificity and selectivity of sounds in a specified manner
finer tuning of sounds; detects finer structure in acoustic signal; recognizes variations in speech
re: postnatal stages of auditory development
describe stage III: flexibility in sound processing - a more “adult” approach to sound
by 8-9 years, child’s separation of sounds are more adult-like; can separate stimuli from noise