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740 Possible Causes for Absent Pulp Chambers, Broad Nasal Bridge

  • Smith-Magenis Syndrome

    In addition, secondary teeth, particularly premolars, might be absent while the other teeth might display enlarged pulp chambers and reduced roots (taurodauntism).[] The main clinical features of this syndrome which is also referred to as the Smith-Magenis syndrome consist of a broad flat midface with brachycephaly, broad nasal bridge,[] The common clinical findings were: speech delay with behavioural problems associated with broad flat midface, brachycephaly, broad nasal bridge and brachydactyly.[]

  • Mucopolysaccharidosis

    BACKGROUND: Mucopolysaccharidosis I is a lysosomal storage disease caused by a deficiency of the enzyme alpha-L-iduronidase. We evaluated the effect of enzyme-replacement therapy with recombinant human alpha-L-iduronidase in patients with this disorder. METHODS: We treated 10 patients with mucopolysaccharidosis I[…][]

    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[] bridge, protruding tongue, high-arched palate, dental abnormalities, and a short and broad neck.[] bridge, broad hands with short fingers, decreased muscle tone, and by trisomy of the human chromosome numbered 21 — called also Down, Down's, trisomy 21 Comments on Down[]

    Missing: Absent Pulp Chambers
  • Pallister-Killian Syndrome

    nasal bridge, short nose with upturned nares, large mouth with downturned corners and prominent upper lip.[] PKS has the following characteristics: low muscle tone facial features that are common to the syndrome-high forehead, broad nasal bridge, wide space between the eyes sparse[] […] profile, high forehead with temporo-frontal balding, sparseness of eyebrows and lashes, shallow supraorbital ridges, upslanting palpebral fissures, hypertelorism, flat and broad[]

    Missing: Absent Pulp Chambers
  • Mucopolysaccharidosis 2

    Summary Epidemiology Prevalence at birth in Europe is 1/166,000. It is an X-linked recessive disorder; very rare cases of female presentation have been reported. Clinical description MPS2 patients appear healthy at birth, with initial symptoms appearing between 18 months and 4 years of age. Macrocephaly develops[…][]

    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[] The eyebrows are bushy and synophyrs may be present across a broad nasal bridge.[]

  • Mucopolysaccharidosis 1

    Summary Epidemiology Prevalence is estimated at 1/100,000, with Hurler syndrome accounting for 57% of cases, Hurler-Scheie syndrome accounting for 23% of cases and Scheie syndrome accounting for 20% of cases. Clinical description In the severe form (Hurler syndrome or MPS I-H; see this term) skeletal deformities[…][]

    Missing: Absent Pulp Chambers
  • Mucopolysaccharidosis 6

    Maroteaux–Lamy syndrome is a form of mucopolysaccharidosis caused by a deficiency in arylsulfatase B (ARSB). [2] It is named after Pierre Maroteaux (1926–) and his mentor Maurice Emil Joseph Lamy (1895–1975), both French physicians. [3] [4] Symptoms [ edit ] Children with Maroteaux–Lamy syndrome usually have[…][]

    Missing: Absent Pulp Chambers
  • Achondroplasia

    Cervicomedullary compression at the foramen magnum in patients with achondroplasia can be associated with apnea, neurological deficits, and sudden death. Decompressive operations are often performed in symptomatic patients. In asymptomatic patients, the indications for prophylactic decompression are controversial.[…][]

    Missing: Absent Pulp Chambers
  • Mowat-Wilson Syndrome

    Facial properties include prominent narrow chin, open mouth, cupped ears with protruding lobes, broad nasal bridge with rounded nasal tip, and wide set eyes.[] Facial features include square-shaped face with deep-set, widely spaced eyes, broad nasal bridge with a rounded nasal tip and a prominent pointed c read more[] Mowat-Wilson syndrome: a genetic ( inherited ) condition present at birth that features square-shaped face with deep-set, widely spaced eyes, a broad nasal bridge , pointed[]

    Missing: Absent Pulp Chambers

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