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526 Possible Causes for Hearing Problem, Hypertelorism, Rarely Malignant

  • Turner Syndrome

    Patients with TS have a higher risk of developing cancer, although multiple malignant tumors are extremely rare.[ncbi.nlm.nih.gov] […] and hearing problems.[house.wikia.com] […] encountered findings were growth delay (98.8%), shortening of the 4 th and 5 th metacarpal bones (74.6%), abnormal nails (73.3%), broad chest (60.7%), short neck (58.6%), hypertelorism[ncbi.nlm.nih.gov]

  • Mucopolysaccharidosis

    Because of the slow progressive nature of this disease and its atypical symptoms, the misdiagnosis of MPS IIIB is not rare in clinical practice.[ncbi.nlm.nih.gov] However, they may present with a variety of physical problems. These may include joint stiffness, heart problems, corneal clouding and hearing loss.[luriechildrens.org] People with MPS IVB can have lots of problems. They can have skeleton, heart, vision and dental problems, hearing loss, growth deficiency and short stature.[thinkgenetic.com]

  • Down Syndrome

    Medulloblastoma, the most common malignant brain tumor of childhood, is particularly rare in the DS population, with only one published case.[ncbi.nlm.nih.gov] They may have hearing problems and problems with the intestines, eyes, thyroid, and skeleton.[medlineplus.gov] Individuals with Down syndrome are at an increased risk for heart, gastrointestinal, hematologic, respiratory, visual, sensory-motor, speech and language and hearing problems[genetics.emory.edu]

  • Noonan Syndrome

    NS patients show a predisposition to malignancy; however, acute lymphoblastic leukemia (ALL) is rarely reported.[ncbi.nlm.nih.gov] Children suspected of having Noonan syndrome should be screened for heart, vision, and hearing problems.[merckmanuals.com] Craniofacial anomalies in affected patients include hypertelorism and severe open bite associated with masticatory dysfunction.[ncbi.nlm.nih.gov]

  • Neurofibromatosis Type 1

    Plexiform neurofibromas- tumors along nerve bundle tracts, can be large and usually appear at birth or early in childhood (occur in 25%) Malignant peripheral nerve sheath[en.wikibooks.org] Hearing aids One option may be to consider a hearing implant. These are surgically implanted electrical devices used to bypass problems in the hearing mechanism.[web.archive.org] NS is a disorder characterized by dysmorphic facial features, short stature, hypertelorism, cardiac anomalies, deafness, motor delay, and a bleeding diathesis.[genome.ucsc.edu]

  • Deafness

    Abstract Keratitis ichthyosis deafness (KID) syndrome is a rare genodermatosis with a high risk of cutaneous malignancy and infections.[ncbi.nlm.nih.gov] Websites Table Of Contents External Websites How Stuff Works - Healthguide - Hearing Loss and Deafness British Broadcasting Corporation - Deafness and Hearing Problems National[web.archive.org] The probands had short stature, hypertelorism, midface hypoplasia, sensorineural hearing loss, normal intelligence as well as slight radial and ulnar bowing with brachytelephalangy[ncbi.nlm.nih.gov]

  • Sensorineural Hearing Impairment

    Primary middle ear neoplasms are rare, and commonly cause conductive hearing loss.[ncbi.nlm.nih.gov] 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] […] reported on MR imaging in 100% of patients with Pendred syndrome. 17 Waardenburg Syndrome Waardenburg syndrome is autosomal dominant with characteristic features, including hypertelorism[ajnr.org]

  • Gorlin Syndrome

    Medulloblastoma, the most common malignant brain tumor of childhood, is particularly rare in the DS population, with only one published case.[ncbi.nlm.nih.gov] Management should be directed towards in-depth investigation, treatment and prevention of associated problems, such as growth retardation, feeding problems, hearing loss,[ncbi.nlm.nih.gov] Because of macrocrania, hypertelorism and epidermal punctiform lesions in the palm of the hand, Gorlin syndrome was clinically suspected and molecularly confirmed by finding[ncbi.nlm.nih.gov]

  • Aarskog-Scott Syndrome

    Severe Malignant Osteopetrosis November 20, 2018 by Peter Ciszewski Osteopetrosis refers to a group of rare, inherited skeletal disorders characterized by increased bone density[checkrare.com] Pediatricians, surgeons, cardiologists, dental specialists, speech pathologists, specialists who asses and treat hearing problems (audiologists), eye specialists, and other[rarediseases.org] As previously reported, 6 carrier females often show minor dysmorphic features such as hypertelorism and widow's peak.[doi.org]

  • Paget Disease of the Bone

    May have gross bony deformity; may be only physical finding Rapid onset of pain and swelling suggests malignant degeneration (rare; less than 1% chance of malignant degeneration[orthopaedicsone.com] The disease can lead to other health problems, too, such as arthritis and hearing loss.[linkedlifedata.com] The nasal bones were also increased in size with hypertelorism, and mandibular contour was normal [Figure 1]. On palpation, enlarged maxilla was bony hard and nontender.[amsjournal.com]

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