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5,297 Possible Causes for 1st Metatarsal Absent, Deafness, Partial Syndactyly of Fingers and Toes

  • Saethre-Chotzen Syndrome

    Patients sometimes have visceral malformations, like heart defects, cryptorchidism or sensorial organ malfunction, such as deafness.[symptoma.com] Unilateral or bilateral coronal synostosis, low frontal hair line, strabismus, ptosis, and partial cutaneous syndactyly of fingers and toes are findings suggestive of the[ncbi.nlm.nih.gov] […] multiple surgeries at an early age Saethre-Chotzen Syndrome does not adversely affect adults unless there was early presence of either slow development, hearing loss, or deafness[wiki.ggc.edu]

  • Impacted Cerumen

    Differential diagnosis Other causes of acute deafness - eg, Eustachian tube dysfunction, foreign body. Otitis externa.[patient.info] Sudden or partial hearing loss, which is usually temporary 2.[info.earwaxmd.com] […] contraindicated if there are any signs or symptoms of current otitis externa or otitis media, past or present tympanic membrane perforation, history of ear surgery or unilateral deafness[racgp.org.au]

    Missing: 1st Metatarsal Absent Partial Syndactyly of Fingers and Toes
  • Patel-Bixler Syndrome

    Craniometaphyseal dysplasia manifests with macrocephaly, proptosis, hypocalcemia, hyperparathyroidism, wide metaphyses, and sensorineural deafness.[ncbi.nlm.nih.gov] CHD7 mutational analysis and clinical considerations for auditory rehabilitation in deaf patients with CHARGE syndrome.[rarediseases.org] syndactyly of fingers and toes.[ncbi.nlm.nih.gov]

    Missing: 1st Metatarsal Absent
  • Otoonychoperoneal Syndrome

    […] myopia Optic atrophy polyneuropathy deafness Optic atrophy, autosomal dominant Optic atrophy, idiopathic, autosomal recessive Optic atrophy Optic nerve coloboma with renal[wikidoc.org] syndactyly of fingers and toes, brachydactyly of toes, valgus def[academicoo.com] syndactyly Talipes equinovarus Toe syndactyly Severe muscular hypotonia Chorioretinal coloboma Plagiocephaly Proximal placement of thumb Abnormal vertebral morphology High[mendelian.co]

    Missing: 1st Metatarsal Absent
  • Meniere's Disease

    Sometimes, it can present as sudden deafness with vertigo, without brainstem or cerebellar signs.[ncbi.nlm.nih.gov] Initially, deafness maybe there only for low frequencies.[symptoma.com] Cases 1 and 2 illustrate treatment of vertigo attacks caused by vestibular dysfunction in deaf ears.[ncbi.nlm.nih.gov]

    Missing: 1st Metatarsal Absent Partial Syndactyly of Fingers and Toes
  • Facioauriculoradial Dysplasia

    MalaCards integrated aliases for Phocomelia-Ectrodactyly, Ear Malformation, Deafness, and Sinus Arrhythmia: Name: Phocomelia-Ectrodactyly, Ear Malformation, Deafness, and[malacards.org] […] tarsal bones and partial cutaneous syndactyly.[mendelian.co] […] of the pinnae), conductive deafness, dysmorphism (long and prominent philtrum, mild maxillary hypoplasia) and sinus arrhythmia.[monarchinitiative.org]

    Missing: 1st Metatarsal Absent
  • Presbycusis

    Deafness is the complete inability to hear sound. Deafness and hearing loss have many causes and can occur at any age.[bodyandhealth.canada.com] […] cochlear nucleus neuron counts without significant cochlear changes, indicating that this pattern of pathological changes is a possible cause of high tone sensorineural deafness[ncbi.nlm.nih.gov] , Age-related hearing loss, Presbyacusia, senile deafness, age related hearing loss, hard of hearing (presbyacusis), presbyacusis, senile presbyacusis, Presbycusis;senile,[fpnotebook.com]

    Missing: 1st Metatarsal Absent Partial Syndactyly of Fingers and Toes
  • Pili Torti

    A maternal uncle of the patient was deaf from birth and his hair had shown the same abnormalities at the same age; an autosomal recessive transmission can be assumed.[ncbi.nlm.nih.gov] ( 2449003 ) Barth JH...Dawber RP 1987 27 Cleft lip and palate, pili torti, malformed ears, partial syndactyly of fingers and toes, and mental retardation: a new syndrome?[malacards.org] Pili torti and nerve deafness Get Update Overview Bjornstad syndrome is an autosomal recessive disorder characterized by sensorineural hearing loss and pili torti.[diseaseinfosearch.org]

    Missing: 1st Metatarsal Absent
  • Otitis Media

    We investigated the usefulness and safety of our cochlear implantation method for two deaf patients with eosinophilic otitis media.[ncbi.nlm.nih.gov] We examined the language understanding ability of four patients with bilateral profound or total deafness due to OMAAV, who underwent CI.[ncbi.nlm.nih.gov] Dept. of Child and Adolescent Health and Development WHO Programme for the Prevention of Blindness and Deafness Issue Date: 2004 Publisher: Geneve : World Health Organization[web.archive.org]

    Missing: 1st Metatarsal Absent Partial Syndactyly of Fingers and Toes
  • Congenital Deafness

    Congenital deafness is either genetically caused or acquired in utero through maternal lifestyle and/or infection.[symptoma.com] The methods by which congenital deafness soon may be diagnosed and the implications for the otologist are discussed.[ncbi.nlm.nih.gov] We examined 16 congenitally deaf adolescents, aged between 16 and 19 years, and 16 normally hearing subjects, matched for gender and age.[ncbi.nlm.nih.gov]

    Missing: 1st Metatarsal Absent Partial Syndactyly of Fingers and Toes

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