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110 Possible Causes for Congenital Ear Deformity, Ectopia Lentis, Hearing Problem

  • Smith-Magenis Syndrome

    Treatment for vision problems and hearing problems may be needed. Sleep therapy and/or medication may be needed to help improve sleep patterns and quality of sleep.[thinkgenetic.com] Ocular findings in our patient include: myopia, iris nodules, loose zonules, and ectopia lentis.[ncbi.nlm.nih.gov] Complications The complications which are associated with persons having Smith Magenis Syndrome include the following: Mood problems Ear infection Back problems Hearing Loss[syndromespedia.com]

  • CHARGE Syndrome

    As CHARGE syndrome is quite rare, some children may not be diagnosed until early childhood when hearing problems and/or slow development become obvious.[gosh.nhs.uk] (congenital) 759.89 Ullrich-Feichtiger syndrome 759.89 VATER syndrome 759.89 Weill-Marchesani syndrome (brachymorphism and ectopia lentis) 759.89 "Whistling face" syndrome[icd9data.com] It's helpful for family and friends, especially to be aware of these sensory issues, as hearing problems have been mistaken as metal retardation for centuries.[verywell.com]

  • Thickened Earlobes-Conductive Deafness Syndrome

    Conductive hearing loss If there is a problem in the ear canal or the middle ear, this causes what is known as a conductive hearing loss.[patient.info] lentis isolated Ectopia pupillae Ectopic coarctation Ectopic ossification familial type Ectopic pregnancy Ectrodactyly cardiopathy dysmorphism Ectrodactyly cleft palate syndrome[bioreference.net] Deformities Absence of the outer ear Congenital deformity or absence of the outer ear, usually on one side, sometimes on both, is often accompanied by absence of the outer-ear[britannica.com]

  • Lens Coloboma

    This is especially true for children with CHARGE, who often also have hearing loss, vestibular (balance) abnormalities and serious medical problems requiring multiple hospitalizations[chargesyndrome.org] We present a case of Marfan syndrome with lens coloboma in one eye and ectopia lentis in the other. A 14-year-old girl reported decreased vision in the left eye.[ncbi.nlm.nih.gov] ICD-10-CM Codes › Q00-Q99 Congenital malformations, deformations and chromosomal abnormalities › Q10-Q18 Congenital malformations of eye, ear, face and neck › Q12- Congenital[icd10data.com]

  • Isolated Ectopia Lentis

    problems  Monitoring temperatures  Large readout thermometers and talking thermometer Sharma IP 71.  Talking colour detector IPS Sharma IP 72.[slideshare.net] We here describe an isolated form of ectopia lentis in a large inbred family that shows autosomal-recessive inheritance.[ncbi.nlm.nih.gov] WHO-ICD-10 version:2010 Congenital malformations, deformations and chromosomal abnormalities Congenital malformations of eye, ear, face and neck Mode of Inheritance Autosomal[cags.org.ae]

  • Goldberg-Shprintzen Syndrome

    Some individuals have problems with their immune system, respiratory issues, kidney abnormalities, low calcium, feeding difficulties, hearing loss, skeletal differences, and[childrensmercy.org] […] age 20 years or older [1] Ectopia lentis syndrome Autosomal dominant Ectopia lentis Variable skeletal manifestations reminiscent of the Marfan syndrome Heterozygous mutations[medicinman.cz] […] and often a deformity of the auricles ("crumpled ears").[aerzteblatt.de]

  • Aniridia

    Related ocular conditions including glaucoma, cataracts, strabismus and optic nerve hypoplasia result in a variety of visual problems.[symptoma.com] It can also appear with other ocular anomalies, such as cataracts, glaucoma, corneal pannus, optic nerve hypoplasia, macular hypoplasia, or ectopia lentis.[ncbi.nlm.nih.gov] ICD-10-CM Codes › Q00-Q99 Congenital malformations, deformations and chromosomal abnormalities › Q10-Q18 Congenital malformations of eye, ear, face and neck › Q13- Congenital[icd10data.com]

  • High Myopia-Sensorineural Deafness Syndrome

    Likewise, vision problems were similar regardless of severity and laterality of hearing loss.[medpagetoday.com] lentis Infantile spasms broad thumbs Tardive dyskinesia Microphthalmia associated with colobomatous cyst Mucopolysaccharidosis type IVA Epidermolysis bullosa Medium-chain[checkrare.com] Renal Ultrasound If syndromal features: preauricular pits or sinuses, deformity of ear, branchial cleft or cysts; Mondini defect on imaging; multiple congenital abnormalities[starship.org.nz]

  • Syndromic Microphthalmia Type 10

    Vestibular symptoms including vertigo, dizziness and balance problems have been reported in Waardenburg Syndrome, even without hearing loss.[californiaearinstitute.com] Congenital lens dislocation AD FBN1 #129600 ECTOPIA LENTIS, ISOLATED Lens dislocation AR ADAMTSL4 #225100 EHLERS-DANLOS SYNDROME Myopia, ectopia lentis, blue sclera, epicanthal[eyewiki.aao.org] ICD-10-CM Codes › Q00-Q99 Congenital malformations, deformations and chromosomal abnormalities › Q10-Q18 Congenital malformations of eye, ear, face and neck › Q11- Anophthalmos[icd10data.com]

  • Noonan Syndrome

    Children suspected of having Noonan syndrome should be screened for heart, vision, and hearing problems.[merckmanuals.com] (congenital) 759.89 Ullrich-Feichtiger syndrome 759.89 VATER syndrome 759.89 Weill-Marchesani syndrome (brachymorphism and ectopia lentis) 759.89 "Whistling face" syndrome[icd9data.com] […] with a thickened helix, and a broad forehead), congenital heart defects and unusual pectus deformity.[orpha.net]

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