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379 Possible Causes for Congenital Clubfoot, Hearing Impairment

  • Alpha-Mannosidosis

    impairment (moderate-to-severe sensorineural hearing loss), gradual impairment of mental functions and speech, and often, periods of psychosis.[ncbi.nlm.nih.gov] In humans, alpha-mannosidosis results in progressive facial- and skeletal abnormalities, motor impairment, hearing impairment, intellectual disability, recurrent infections[ncbi.nlm.nih.gov] The disease characterized by mental retardation, skeletal changes, hearing impairment, and recurrent infections.[ncbi.nlm.nih.gov]

  • Ehlers Danlos Syndrome

    Other problems related to the joint hypermobility are joint instability, foot deformities such as congenital clubfoot or pes planus, temporomandibular joint dysfunction, joint[nature.com] The focus of this study was to evaluate the prevalence, type, and severity of hearing impairment in patients with Ehlers-Danlos Syndrome (EDS) and to compare these characteristics[ncbi.nlm.nih.gov] Congenital multiple contractures, characteristically adduction-flexion contractures and/or talipes equinovarus (clubfoot); 2.[raredr.com]

  • Nail-Patella Syndrome

    Orthopedic surgery may be necessary for congenital clubfoot deformity. Manipulation or surgery may be required to correct hip dislocation.[encyclopedia.com] We identified normal-tension glaucoma (NTG) and sensorineural hearing impairment as new symptoms associated with NPS.[ncbi.nlm.nih.gov] Sensorineural hearing impairment has also been associated with NPS (Bongers et al., 2005).[preventiongenetics.com]

  • Pancreatic Insufficiency - Anemia - Hyperostosis Syndrome

    Mental and behavioural disorder H00903 Congenital clubfoot Congenital talipes equinovarus Congenital clubfoot is an idiopathic deformity of the lower limb that consists of[kegg.jp] Related symptoms: Autosomal dominant inheritance Hearing impairment Scoliosis Growth delay Micrognathia SOURCES: UMLS MONDO OMIM GARD ORPHANET More info about MANDIBULAR[mendelian.co] Complete visual loss invariably occurs in all untreated patients, and hearing loss is estimated to affect 78% of patients with OPT.[mendelian.co]

  • Congenital Muscular Dystrophy

    Fig 2 Bilateral congenital clubfoot in patient D-05 (case 2). Photograph reproduced with permission of parents.[academic.oup.com]

  • Joint Contracture

    We present a new patient of this syndrome, with frequent fractures, congenital joint contractures, kyphoscoliosis, bilateral clubfoot, and pectus carinatum.[ncbi.nlm.nih.gov] HEALTH SEARCH Physically Handicapped Visually Handicapped Mentally Retarded Hearing Impaired Leprosy Cured Parenting Learning Disabilities Physical Disabil... click on following[endoflifecare.tripod.com]

  • Osteogenesis Imperfecta

    This paper presents the case of a child with OI type IV who, at birth, was also diagnosed with a severe clubfoot (congenital talipes equinovarus) grade III.[ncbi.nlm.nih.gov] In some cases, hearing impairment and brittle, discolored teeth (dentinogenesis imperfecta) may also be present.[rarediseases.org] Hearing impairment begins in the third decade due to otosclerosis (a disorder of the bones of the middle ear).[medicinenet.com]

  • Craniofrontonasal Dysplasia

    C. - "CONGENITAL CLUBFOOT: PATHANATOMY AND TREATMENT" - THE AMERICAN ACADEMY OF ORTHOPEDIC SURGEONS: INSTRUCTIONAL COURSE LECTURES, VOL. 36, ST.[graduo.ro] […] hairline Joint hypermobility Low posterior hairline Microcephaly Muscular hypotonia Oral cleft Plagiocephaly Preaxial foot polydactyly Sandal gap Scoliosis Sensorineural hearing[familydiagnosis.com] impairment 0000407 Sprengel anomaly High shoulder blade 0000912 Thickened nuchal skin fold Thickened skin folds of neck Thickened skin over the neck [ more ] 0000474 Widow's[rarediseases.info.nih.gov]

  • Isolated Klippel-Feil Syndrome

    C. - "CONGENITAL CLUBFOOT: PATHANATOMY AND TREATMENT" - THE AMERICAN ACADEMY OF ORTHOPEDIC SURGEONS: INSTRUCTIONAL COURSE LECTURES, VOL. 36, ST.[graduo.ro] ; Congenital muscular torticollis ; Ectopic anus ; Facial asymmetry ; Hearing impairment ; Hemiplegia/hemiparesis ; Low posterior hairline ; Renal hypoplasia/aplasia ; Scoliosis[mousephenotype.org] Hearing impairment in patients with isolated MD may be caused by factors other than mutations in the SLC26A4 gene.[scienceopen.com]

  • Spondylocarpotarsal Synostosis

    An autosomal recessive disorder (OMIM:272460) characterised by: short stature; vertebral, carpal and tarsal fusion; joint laxity; congenital inguinal hernias; clubfoot; and[medical-dictionary.thefreedictionary.com] impairment ; Pes planus ; Preauricular skin tag ; Renal cyst ; Restrictive ventilatory defect ; Scoliosis ; Sensorineural hearing impairment ; Short neck ; Short nose ; Talipes[mousephenotype.org] […] inguinal hernias, clubfoot, and peculiar facies (hypertelorism, short nasal septum, and broad bridge and tip of the nose). {7:Langer et al. (1994)} reported 6 additional[bio2rdf.org]

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