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13 Possible Causes for Dysmorphic Face, Variable Malocclusions, Vertigo

  • Osteogenesis Imperfecta

    The sclera have variable hues. In utero fractures are common. Limb shortening and progressive deformities can occur.[web.archive.org] […] also a common feature. 1, 3 Otologic manifestations of OI occur in approximately 50% of patients and include hearing loss, the most common problem, as well as tinnitus, vertigo[jamanetwork.com] Vertigo is a troublesome symptom in many people with OI including OI type 1 [Kuurila et al., 2003 ].[onlinelibrary.wiley.com]

  • Pyknodysostosis

    The patient presented the mouth deformity described by most of the reports, however, as the three cases reported by Hunt et al, presented different types of malocclusion ([jisppd.com] Bony overgrowth and sclerosis of the skull base cause variable compression of cranial nerves VII and VIII, resulting in peripheral facial nerve palsy and vertigo (Beighton[rrnursingschool.biz] […] accentuated overbite, bilateral cross bite, and biprotrusion, respectively), it may be considered that the presentation of the relationship between the arches is variable.[jisppd.com]

  • Kabuki Syndrome

    Kabuki syndrome is a rare autosomal dominant trait with variable clinical expression.[ncbi.nlm.nih.gov] A 13-year-old girl with Kabuki make up syn-drome presented with mental and physical retarda-tion, submucosal cleft palate, epileptic seizure and had complained of vertigo[webview.isho.jp] It is characterized by a dysmorphic face, postnatal growth retardation, skeletal abnormalities, mental retardation, and unusual dermatoglyphic patterns.[ncbi.nlm.nih.gov]

  • King Syndrome

    The presence of a myopathy associated with a predisposition to malignant hyperthermia suggests an autosomal dominant pattern of inheritance with variable expression.[zdoc.site] Tinnitus and Vertigo, New York: Nelson, p 280. 8.[noiseandhealth.org] face.[idocslide.com]

  • Cri Du Chat Syndrome

    malocclusion, more commonly anterior open-bite.[ncbi.nlm.nih.gov] , was admitted to our departmentwith sudden loss of consciousness, vomiting, and incontinence.After a few hours she recovered consciousness, but she hadanxmia, headache, vertigo[vdocuments.com.br] The clinical signs include a characteristic craniofacial dysmorphism (microcephaly, round face, hypertelorism) which evolves with age, and intellectual disability.[fondationlejeune.org]

  • Pyle's Disease

    […] weakness; - scoliosis, genu valgum deformity, dental / malocclusion and bone fragility; - marked expansion of the metaphyseal segments of tubular leads to an "Erlenmeyer[wheelessonline.com] ., Intratympanic corticosteroids for Meniere’s disease and vertigo Otolaryngol Clin N Am. 2004; 37: 955-972.[revista.acorl.org] […] hypotrophy syndrome Intellectual disability-craniofacial dysmorphism-cryptorchidism syndrome Intellectual disability-developmental delay-contractures syndrome Intellectual[se-atlas.de]

  • Isolated Trigonocephaly

    There may associated FGFR3 mutation and phenotypic variability between generations is a common observation. Apert syndrome was described by Apert in 1906.[childneurosurgeon.com] […] cell hidradenoma 【明細胞癌】*clear cell carcinoma 【明細胞性棘細胞腫】*clear cell acanthoma (迷) 【迷走神経炎】*vagitis 【迷入膵】*aberrant pancreas 【迷入唾液腺】*aberrant salivary gland (眩) 【眩暈】*dizziness *vertigo[medo.jp] Crouzon craniofacial dysostosis (OMIM 123500) involves only the face and skull.[rrnursingschool.biz]

  • Osteogenesis Imperfecta Type 2

    The affected persons’ posture, weight and size of the head are often abnormal and these variables may contribute to the development of the Skeletal Class III malocclusion.[nature.com] Conductive or mixed hearing loss occurs in about 50% of families, beginning in the late teens and leading, gradually, to profound deafness, tinnitus, and vertigo by the end[ibis-birthdefects.org] His sclerae had a faint bluish hue and his face had no appreciable dysmorphic features.[jmg.bmj.com]

  • Osteogenesis Imperfecta Type 15

    The affected persons’ posture, weight and size of the head are often abnormal and these variables may contribute to the development of the Skeletal Class III malocclusion.[nature.com] Additional features of OI include hearing loss of conductive or mixed type in about 50% of families, tinnitus, and vertigo.[ 3 ] Furthermore thin, easily bruised skin, moderate[edoj.org.eg] His sclerae had a faint bluish hue and his face had no appreciable dysmorphic features.[jmg.bmj.com]

  • Auriculocondylar Syndrome

    Glossoptosis, masticatory abnormalities, orthodontic problems, and malocclusion occur in a majority of affected subjects.[semanticscholar.org] , see Ménière disease AUH defect , see 3-methylglutaconyl-CoA hydratase deficiency aural vertigo , see Ménière disease Auricular Fibrillation , see familial atrial fibrillation[herenciageneticayenfermedad.blogspot.com] Malocclusion was classified based on Angle and Martin Dewey classification.[repository.trisakti.ac.id]

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