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1,600 Possible Causes for Absent Pulp Chambers, Broad Nasal Bridge, Hyperextensible Joints

  • Mucopolysaccharidosis

    It is marked by shortness and hyperextension of the neck causing the head to appear as if it were resting directly on the shoulders, short trunk, long extremities with excessive[] Careful positioning and avoidance of hyperextension of the neck are necessary.[] joint mobility, kyphosis or kyphoscoliosis, pectus carinatum, the sternum extending from clavicular junction and angling downward in midsection, spinal cord compression associated[]

    Missing: Absent Pulp Chambers
  • Down Syndrome

    bridge, broad hands with short fingers, decreased muscle tone, and by trisomy of the human chromosome numbered 21 — called also trisomy 21 First Known Use of Down syndrome[] hyperextensibility or hyperflexibility Neuromuscular hypotonia Diastasis recti Dry skin Premature aging Congenital heart defects Complications of Down syndrome can involve[] bridge, protruding tongue, high-arched palate, dental abnormalities, and a short and broad neck.[]

    Missing: Absent Pulp Chambers
  • SHORT Syndrome

    Another related syndrome "familial otodentodysplasia" is characterized by the posterior teeth with abnormal morphology, large pulp chambers, short root length compared to[] The primary diagnostic criteria [1] include short stature, hypertelorism, a broad nasal bridge, a short nose with anteverted nares, a long philtrum, maxillary hypoplasia with[] The facial appearance and some of the features resemble the SHORT syndrome, the name being an acronym for Short stature, Hyperextensible joints, Ocular depression, Rieger[]

  • Rubinstein-Taybi Syndrome

    nasal bridge, triangular mouth and pointed chin and skeletal finding including broad great thumbs and halluces, and accessory nipple.[] joints • Small tilted pelvis • Excessive hairiness • Undescended testicles • Feeding difficulties • Respiratory infection • Cardiac anomalies • Vertebral abnormalities •[] Extra oral features revealed distinctive facial appearance with a broad fore head, hypertelorism, broad nasal bridge and beaked nose.[]

    Missing: Absent Pulp Chambers
  • Autosomal Dominant Hyper-IgE Syndrome

    Other clinical manifestations include characteristic facies (prominent forehead, broad nasal bridge and facial asymmetry), chronic eczematous dermatitis, retained primary[] Nonimmunologic manifestations of HIES include a characteristic face, pathologic dentition, scoliosis, bone alterations, hyperextensible joints, and vascular abnormalities.[] nasal bridge Scoliosis Dental - baby teeth do not fall out at the usual time Reduced bone density Eye complications Who is affected?[]

    Missing: Absent Pulp Chambers
  • Aarskog-Scott Syndrome

    The major facial manifestations of this syndrome include hypertelorism, broad forehead, broad nasal bridge, short nose with anteverted nostrils, long philtrum, widow's peak[] By contrast, palpebral ptosis, syndactyly, joint hyperextension and hernias were documented less frequently in nonmutated patients.[] bridge Broad nasal bridge Broad nasal root Broadened nasal bridge Increased breadth of bridge of nose Increased breadth of nasal bridge Increased width of bridge of nose[]

    Missing: Absent Pulp Chambers
  • 3M Syndrome Type 1

    nasal bridge, shallow supraorbital ridge, broad nasal tip, short palpebral fissures, telecanthus, ptosis and dysplastic ears), microcephaly, mental deficiency, and infantile[] Then, during childhood tall vertebral bodies, hip dislocation, transverse chest groove, winged scapulae and hyperextensible joints became more evident and the diagnosis of[] Dubowitz syndrome : includes characteristic facial appearance (small face with sloping forehead, broad nasal bridge, shallow supraorbital ridge, broad nasal tip, short palpebral[]

    Missing: Absent Pulp Chambers
  • Dubowitz Syndrome

    nasal bridge, dysplastic auricles, and retrognathia, is presented.[] Microcephaly, short stature, leg length discrepancy, hyperextensible joints, spina bifida occulta, and absence of anterior cruciate ligaments were present.[] Major clinical findings are intrauterine and postnatal growth retardation, considerable microcephaly, mild mental retardation, hyperactivity, hyperextensibility of joints,[]

    Missing: Absent Pulp Chambers
  • Autosomal Dominant Prognathism

    (short stature) oral manifestation: large pulp chambers, large pulp horns, cracks in dentin all the way to DEJ that may allow bacteria to get in and cause pulpal infections[] bridge, epicanthus, upturned nose IS Retinoblastoma-1 RB1 13q14.1-q14.2 180200 Retinoblastoma 180200 AD cleft palate, high forehead, prominent eyebrows, broad nasal bridge[] Common findings among patients were recurrent fractures (in 57 percent of patients), hyperextensible joints (in 68 percent), and scoliosis (in 76 percent of patients 16 years[]

  • Coffin-Lowry Syndrome

    nasal bridge having thick cartilage (septum) Thick prominent lips with prominent chin and underdeveloped upper jaw Prominent ears Small head Dental anomalies Abnormalities[] joints, muscle atrophy, large and soft hands with simian crease, and tapering of the fingers.[] nasal bridge with a thick dividing cartilage (septum), thick prominent lips, an open mouth, prominent chin and ears.[]

    Missing: Absent Pulp Chambers

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