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317 Possible Causes for Abnormal Dentition, Congenital Facial Anomaly, Respiratory Disorders

  • Cleidocranial Dysplasia

    dentition).[] Cleidocranial dysplasia (CCD) is a rare congenital disorder characterized by skeletal and dental anomalies.[] Causes Cleidocranial dysplasia is a rare disorder that is usually inherited as an autosomal dominant genetic trait.[]

  • Bruxism

    There can be other indications for rebuilding a patient’s dentition.[] PURPOSE: The aim of this study was to evaluate the association between respiratory disorders and sleep bruxism, with an evaluation of demographic/socioeconomic factors and[] Breathing Difficulties - If the patient is suffering any respiratory disorders, including allergies they need to see their doctor for investigation and management.[]

  • Dental Caries

    ., before 7 years of age, abnormalities in the structure of the dental enamel can occur.[] Interestingly, the connections between oral microbes and health extend beyond the oral cavity, as cardiometabolic, respiratory, and immunological disorders, gastrointestinal[] […] during the child’s first 3 years such as such as mumps, diphtheria, scarlet fever, measles, hypoparathyroidism, malnutrition, malabsorption, hypovitaminosis D, chronic respiratory[]

  • Mandibulofacial Dysostosis

    dentition, choanal atresia and mandibular retrusion, external ear malformations and conductive hearing loss. [2] [3] Ocular findings in Treacher Collins syndrome include:[] Castillo M, Mukherji SK (1995) Imaging of facial anomalies. Curr Probl Diagn Radiol 25:169–188 PubMed Google Scholar 3.[] Upper airway obstruction may be a complication from craniofacial disorders and may be responsible for life-threatening sleep apnea that may result in pneumonia or respiratory[]

  • Goldenhar Syndrome

    If a type I deformity presents late in adulthood, then bilateral mandibular osteotomies are required to prevent abnormal forces from acting on the normal TMJ.[] […] genito-urinary anomalies 10 congenital cardiac anomalies 2 Antenatal ultrasound Individual features are non specific.[] Because of spine curves, short trunks and respiratory issues, some children with Goldenhar syndrome will develop thoracic insufficiency syndrome, a very rare disorder characterized[]

  • Seckel Syndrome

    Growth failure is seen in chromosomal disorders and endocrine, metabolic, or gastrointestinal disorders, including malnutrition.[] Due to this fact, some patients have additional clinical findings, such as large bulging skull, cleft palate, atresia palate, abnormalities in dentition, among these, dental[] Abnormalities that suggest alternative diagnoses include congenital anomalies of the face, limbs, heart, or viscera; recurrent infections (other than otitis media or respiratory[]

  • Sanjad-Sakati Syndrome

    dentition and increased susceptibility to infection.[] It is characterized by the association of congenital hypothyroidism, growth retardation, psychomotor retardation, epilepsy, dysmorphic features (microcephaly, facial, eye,[] respiratory infections, and constipation.[]

  • Kabuki Syndrome

    Higher frequencies of neonatal complications, abnormal dentition, hypotonia, and microcephaly were noted in non-Asian patients with NKS, while a higher frequency of skeletal[] Kabuki syndrome is a rare genetic disorder characterized by intellectual disability and multiple congenital anomalies, including short stature, peculiar facial appearance,[] Anesthesiologists should be aware of possibly difficult tracheal intubation cardiac lesions, respiratory problems, neurological and musculoskeletal disorders, and a latex[]

  • Wiedemann-Steiner Syndrome

    […] of the dentition Abnormal dentition Abnormal teeth Dental abnormalities Dental abnormality [ more ] 0000164 Aggressive behavior Aggression Aggressive behaviour Aggressiveness[] Wiedemann-Steiner syndrome (WSS) is an autosomal dominant congenital anomaly syndrome characterized by hairy elbows, dysmorphic facial appearances (hypertelorism, thick eyebrows[] Respiratory disorders, hypertrichosis, and early death uniquely characterize the marshall-smith syndrome.[]

  • Hidrotic Ectodermal Dysplasia

    […] ectodermal dysplasia (AED) is a rare genetic disorder characterized by faulty development of ectodermal structures, resulting most notably in anhidrosis, hypotrichosis and abnormal[] anomaly disorder characterized by bone abnormalities, distinctive facial features, multiple exostoses, and intellectual disability.[] Some individuals with the disorder have unusually thin and brittle nails.[]