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801 Possible Causes for Low-Set, Malformed Ears

  • Microtia

    malformation of ear ossicles Q16.4 Other congenital malformations of middle ear Q16.5 Congenital malformation of inner ear Q16.9 Congenital malformation of ear causing impairment[] But to some low-set remnant ears, it is difficult to manipulate the conventional lobule transposition method in clinical application.[] Anotia means absence of ear Most severe form of microtia Low-set hairline very common Ear smaller than normal Many normal features preserved Can occur with or without an ear[]

  • Branchio-Oculo-Facial Syndrome

    malformation (incomplete partition type II, enlarged vestibule, and enlarged vestibular aqueduct).[] Abstract We present an 18-day old boy with bilateral cervical cutaneous defect in the retroauricular region, low-set and posteriorly rotated ears, bilateral microphtalmia[] We report a 2-month-old boy with bilateral branchial cleft anomalies, low-set ears, and hydronephrosis who tested positive for a mutation in the TFAP2A gene (A256V) implicated[]

  • Patau Syndrome

    Nose: absent, malformed or proboscis (prominent). Ears: malformed ears. Eye: structural eye defects (microphthalmia, iris coloboma or even absence of the eyes).[] It leads to a variety of abnormalities that include mental retardation, microcephaly, low-set ears, eye structural defects, polydactyly, and limb abnormalities The presence[] ears or dysplastic type of ears Abnormal testes or they are undescended Causes of Patau Syndrome It is caused due to the trisomy of chromosome 13.[]

  • Trisomy 18

    […] poor motor ability, micrognathia, microcephaly, low-set and malformed ears, distinctively clenched fists with overlapping fingers, and congenital heart defects.[] During ultrasonographic examination, we discovered that her fetus had several important abnormalities, including a cystic hygroma, craniofacial defects (low-set ears, broad[] ears, rocker-bottom feet, dorsiflexed hallux, hypoplastic nails, short neck, and wrist deformity.[]

  • Ear Deformity

    (congenital) - see also Anomaly ear Q17.9 external Q17.9 ICD-10-CM Codes Adjacent To Q17.9 Q16.5 Congenital malformation of inner ear Q16.9 Congenital malformation of ear[] However, to date, the only frequent otologic deformity recorded in the published literature has been low-set ears.[] In the most severe deformities, there may be need for correction of a forward tilt of the ear and or evening a low set ear to match the other side.[]

  • Pelviscapular Dysplasia

    ears, dysplasia of conchae, a small chin, a short neck with redundant skin folds, and a low hairline.[] List: Pelviscapular dysplasia Symptoms and clinical features may include: 1 Clinical Features of Pelviscapular dysplasia : Macrocephaly Hypertelorism Hearing impairment Low-set[] […] external ears, dysplasia of conchae, small chin, short neck with redundant skin folds, low hairline, and mild psychomotor retardation.[]

  • Noonan Syndrome

    This condition is associated with short stature, heart defects, bleeding disorders, delayed puberty, and skeletal malformations.[] […] nipples, undescended testicles, abnormal facial characteristics (e.g., bright blue or green colored iris, wide-spaced eyes, low-set fleshy ears).[] , choanal atresia, retardation of growth and development, genital abnormalities, and ear malformations association Congenital absence of heart structure Congenital anomaly[]

  • Goldenhar Syndrome

    The syndrome is characterized by the presence of dermal epibulbar tumors, periauricular appendices, malformed ears, and vertebral anomalies, with occasional occurrence of[] […] hairline, mandibular hypoplasia, low-set ears, and sometimes smallness of the mouth on one side.[] RESULTS: Among the 14 patients with Goldenhar syndrome, 13 had outer and middle ear anomalies and 5 (36%) had inner ear malformations, including one case of common cavity.[]

  • Conductive Hearing Loss

    Mutation screening in 169 sporadic cases with external ear and middle ear malformations identified no pathogenic variant or polymorphism.[] Recognition of low-set or malformed auricles with a unilateral or bilateral conductive hearing loss should alert the otolaryngologist to possible middle ear abnormalities[] We here report a family with right-sided external ear malformations and conductive hearing loss in a grandfather, his daughter and granddaughter.[]

  • External Auditory Canal Aplasia/Hypoplasia

    malformations of ear Q17.0 Accessory auricle Q17.3 Other misshapen ear Q17.8 Other specified congenital malformations of ear Q17.9 Congenital malformation of ear, unspecified[] Other symptoms may include down-slanting eyes, skins fold over the inner corners of the eyes ( epicanthal folds ), a small jaw, cleft palate, low set ears, and drooping eyelids[] Ear malformations were almost always associated with hearing loss. Hearing loss was rare in patients with DC and SDS.[]

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