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16 Possible Causes for Hearing Problem, Multiple Congenital Anomalies, Variable Malocclusions

  • Kabuki Syndrome

    […] frequent infections hearing problems or hearing loss congenital heart defects, including coarctation of the aorta, ventricular septal defect and atrial septal defect endocrine[] Kabuki syndrome is a rare autosomal dominant trait with variable clinical expression.[] BACKGROUND: Kabuki syndrome (Niikawa-Kuroki syndrome) is a rare, multiple congenital anomalies/mental retardation syndrome characterized by a peculiar face, short stature,[]

  • Cleidocranial Dysplasia

    An otologist should check for hearing problems. The bone symptoms cause few problems in most cases. Appropriate dental care is important.[] […] numbers of supernumerary teeth along with dental crowding, and malocclusion Hand abnormalities including brachydactyly, tapering fingers, and short, broad thumbs Short stature[] An otologist should check for hearing problems. Outlook (Prognosis) The bone symptoms usually cause few problems. Appropriate dental care is important.[]

  • Cri Du Chat Syndrome

    Only a few have visual or hearing problems, but many have a hypersensitivity to noise, showing this as fear of particular sounds.[] malocclusion, more commonly anterior open-bite.[] A female infant presented at birth with hypotonia, growth retardation, distinctive facies, multiple congenital anomalies, and a high-pitched mewing cry characteristic of cri[]

  • Gorlin-Chaudhry-Moss Syndrome

    Pediatricians, surgeons, cardiologists, dental specialists, speech pathologists, specialists who assess and treat hearing problems (audiologists), eye specialists, and others[] Class II or III malocclusion. Open bite. Facial bone formation Hypoplasia of the malar bones. Hypoplastic lateral aspects of orbits.[] Disease definition Gorlin-Chaudhry-Moss (GCM) syndrome is a multiple congenital anomaly syndrome characterized by craniofacial dysostosis, facial dysmorphism, conductive hearing[]

  • Dubowitz Syndrome

    Hearing problems have not been reported, but vision problems such as problems seeing things up close (farsightedness) and cataracts (clouding of the eye lens) have been reported[] Associations have been made with hyperactivity (4G" variable clefts of the soft palate (10% to 15%), poor feeding and gastroesophageal reflux (33%), chronic diarrhea (35%)[] This group will include 50% with chromosomal disorders congenital anomaly syndromes, especially recognizable by performing a karyotype, the details about their features and[]

  • Osteogenesis Imperfecta

    Other complications can include hearing problems, breathing problems, a blue tint to the eyes, short stature and other complications.[] The sclera have variable hues. In utero fractures are common. Limb shortening and progressive deformities can occur.[] Winter and Michael Baraitser, A catalogue of multiple congenital anomaly syndromes, Multiple Congenital Anomalies, 10.1007/978-1-4899-3109-2_1, (1-672), (1991).[]

  • King Syndrome

    This is a common condition reported in 5 - 10% of those attending clinics complaining of hearing problems.[] The presence of a myopathy associated with a predisposition to malignant hyperthermia suggests an autosomal dominant pattern of inheritance with variable expression.[] This group will include 50% with chromosomal disorders congenital anomaly syndromes, especially recognizable by performing a karyotype, the details about their features and[]

  • Kohlschütter-Tönz Syndrome

    Heart disease Skin manifestations Autism Behavioral Problems: might include hyperactivity, aggressive behavior, tantrums Seizures: sudden episodes of electrical activity[] […] in muscle fiber diameter Abnormal isoelectric focusing of serum transferrin Delayed myelination Poor suck Deep palmar crease Nail dysplasia Trigonocephaly Dental malocclusion[] In this paper, we review the dental anomalies in several multiple congenital anomaly (MCA) syndromes, in which the dental component is pivotal in the recognition of the phenotype[]

  • Isolated Trigonocephaly

    Most of these patients tend to exhibit raised ICP, hydrocephalus, optic atrophy and respiratory, speech and hearing problems.[] There may associated FGFR3 mutation and phenotypic variability between generations is a common observation. Apert syndrome was described by Apert in 1906.[] The C syndrome also known as Opitz trigonocephaly syndrome is a multiple congenital anomaly/mental retardation (MCA/MR) syndrome.[]

  • Osteogenesis Imperfecta Type 16

    Flat feet Dislocations Kidney Stones Gastrointestinal problems Hearing loss Heart problems As each person is unique, no one person with Osteogenesis Imperfecta has exactly[] 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.[] There also may be associated problems such as congenital anomalies, respiratory insufficiency, and neurological problems.[]