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Whilst hearing loss is a common symptom in many diseases of the ear, for example in otosclerosis (abnormal bone growth in the ear), [3] the white, chalky patches on the tympanic membrane are fairly characteristic of tympanosclerosis. Cholesteatoma is similar in appearance but the whiteness is behind the tympanic membrane, rather than inside.
Juvenile hyaline fibromatosis (also known as fibromatosis hyalinica multiplex juvenilis [2] and Murray–Puretic–Drescher syndrome [2]) is a very rare, autosomal recessive disease due to mutations in capillary morphogenesis protein-2 (CMG-2 gene).
White–Sutton syndrome is named for doctors Janson White, Ph.D. and V. Reid Sutton, M.D. [5] In his role as a clinical researcher with the Baylor-Johns Hopkins Center for Mendelian Genomics, Sutton worked with graduate student Janson White on the description of the spectrum of developmental and health issues in individuals with variants in the POGZ gene, first detailed in White's paper, "POGZ ...
The Guidelines on the Treatment of Adults with Vestibular Schwannoma issued in 2018 by the Congress of Neurological Surgeons in the U.S. looked at the long-term evolution of treatments for VS. The Introduction to the Guidelines stated: "The evolution in treatment over the last century has ultimately led to an environment where functional ...
The use of technology has begun to be implemented in ABA therapy for the treatment of autism. [49] Robots, gamification, image processing, story boards, augmented reality, and web systems have been shown to be useful in the treatment of autism. [49] These technologies are used to teach children with autism skill acquisition. [49]
Autism is associated with several genetic disorders, [4] perhaps due to an overlap in genetic causes. [5] About 10–15% of autism cases have an identifiable Mendelian (single-gene) condition, chromosome abnormality, or other genetic syndrome, [6] a category referred to as syndromic autism.
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hearing loss, including temporary hearing loss, such as from ear infections; developmental disorders (e.g. autism) neurological disorders (e.g. cerebral palsy) cleft palate or other physical anomalies of the mouth Functional causes These are cases where there is no identifiable physical cause:
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