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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[childrenshospital.org] Kabuki syndrome is a rare autosomal dominant trait with variable clinical expression.[ncbi.nlm.nih.gov] BACKGROUND: Kabuki syndrome (Niikawa-Kuroki syndrome) is a rare, multiple congenital anomalies/mental retardation syndrome characterized by a peculiar face, short stature,[ncbi.nlm.nih.gov]

  • Cleidocranial Dysplasia

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

  • 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.[members.tripod.com] malocclusion, more commonly anterior open-bite.[ncbi.nlm.nih.gov] A female infant presented at birth with hypotonia, growth retardation, distinctive facies, multiple congenital anomalies, and a high-pitched mewing cry characteristic of cri[ncbi.nlm.nih.gov]

  • Gorlin-Chaudhry-Moss Syndrome

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

  • 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[rarediseases.org] 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%)[healio.com] This group will include 50% with chromosomal disorders congenital anomaly syndromes, especially recognizable by performing a karyotype, the details about their features and[books.google.com]

  • Osteogenesis Imperfecta

    Other complications can include hearing problems, breathing problems, a blue tint to the eyes, short stature and other complications.[nicklauschildrens.org] The sclera have variable hues. In utero fractures are common. Limb shortening and progressive deformities can occur.[web.archive.org] 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).[doi.org]

  • King Syndrome

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

  • Kohlschütter-Tönz Syndrome

    Heart disease Skin manifestations Autism Behavioral Problems: might include hyperactivity, aggressive behavior, tantrums Seizures: sudden episodes of electrical activity[australasianleukodystrophyfoundation.com] […] in muscle fiber diameter Abnormal isoelectric focusing of serum transferrin Delayed myelination Poor suck Deep palmar crease Nail dysplasia Trigonocephaly Dental malocclusion[mendelian.co] 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[lirias.kuleuven.be]

  • Isolated Trigonocephaly

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

  • 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[hypermobility.org] 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] There also may be associated problems such as congenital anomalies, respiratory insufficiency, and neurological problems.[books.google.ro]