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1,798 Possible Causes for Absent Pulp Chambers, Congenital Ear Deformity, Low Set Ears

  • 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).[] ears, and brachydactyly.[] Craniofacial and skeletal abnormalities are common, including brachycephaly, broad nasal bridge, flat midface, tented upper lip, synophrys, hypertelorism, abnormally shaped or low-set[]

  • Patau Syndrome

    This includes scalp defects, coloboma, hypertelorism, cleft lip, cleft palate, deformed ears, congenital heart disease, microcephaly, sloping forehead, wide sagittal suture[] It leads to a variety of abnormalities that include mental retardation, microcephaly, low-set ears, eye structural defects, polydactyly, and limb abnormalities The presence[] Cutis aplasia (missing portion of the skin/hair) Prominent heel Microcephaly Low-set ears Cleft palate or hare lip Collection Procedure • Amniotic fluid Discard the first[]

    Missing: Absent Pulp Chambers
  • Turner Syndrome

    Other characteristics, like widely spaced nipples or low-set ears, also may lead to a suspicion of Turner syndrome.[]

    Missing: Absent Pulp Chambers
  • CHARGE Syndrome

    Ear abnormalities and deafness – most children with CHARGE syndrome have some level of hearing impairment, varying from mild to profound, along with underdeveloped or low-set[] The most common external ear anomalies include low-set ears, asymmetric ears, or small or absent ear lobes. The degree of hearing loss varies from mild to severe.[] These may include: a square-shaped face facial asymmetry, a difference in the appearance between the right and left sides of the face low-set and abnormal appearing ears antimongoloid[]

    Missing: Absent Pulp Chambers
  • Ear Deformity

    The aim of this article was to describe a novel technique for fabricating ear prosthesis in a patient with congenital ear deformity.[] However, to date, the only frequent otologic deformity recorded in the published literature has been low-set ears.[] In the most severe deformities, there may be need for correction of a forward tilt of the ear and or evening a low set ear to match the other side.[]

    Missing: Absent Pulp Chambers
  • Miller Dieker Syndrome

    They have low set ears, severe vision problems , a high forehead and a small mouth with a wide upper lip.[] […] forehead with furrows and vertical ridges, indentation of the temples, a small, upturned nose, up-slanting eyes, a small mouth, a thick, broad upper lip with a thin border, low-set[] Other signs and symptoms of Miller Dieker syndrome include: • severe mental retardation; • low set ears; • severe visual problems; • high forehead; • small mouth with a wide[]

    Missing: Absent Pulp Chambers
  • Trisomy 20

    At external examination of the fetus we detected only low-set ears and no other abnormalities. Internally, all organs appeared normal macroscopically.[] However, the fetus, under macro- and microscopic analysis, showed only two minor anomalies: left simian crease and low-set ears.[] The most consistent phenotypic abnormalities include intrauterine growth retardation, low-set ears (frequently associated with microtia of varying degrees plus tags/pits),[]

    Missing: Absent Pulp Chambers
  • Microtia

    Microtia Microtia (meaning 'Small ear') is a congenital deformity of the outer ear.[] But to some low-set remnant ears, it is difficult to manipulate the conventional lobule transposition method in clinical application.[] Arturo Bonilla’s Microtia-Congenital Ear Deformity Institute has evaluated thousands of children born with microtia and atresia. Dr.[]

    Missing: Absent Pulp Chambers
  • Hallermann-Streiff Syndrome

    Absence of, with Taurodontia and Sparse Hair Tetramelic Deficiencies, Ectodermal Dysplasia, Deformed Ears, and Other Abnormalities Thumb Deformity and Alopecia Trichodental[] We describe a 20-year-old female patient whose clinical findings mostly fall into this syndrome, except for the presence of slightly low-set ears.[] View map Stories of Hallermann Streiff Syndrome HALLERMANN STREIFF SYNDROME STORIES VIEWS BY SURPRISE normal pregnancy. normal birth. due to low set ears and big forhead recommended[]

    Missing: Absent Pulp Chambers
  • Trisomy 18

    Characteristics of the syndrome include severe mental and growth retardation; congenital heart disease and other internal defects; and a multitude of bodily deformities, such[] During ultrasonographic examination, we discovered that her fetus had several important abnormalities, including a cystic hygroma, craniofacial defects (low-set ears, broad[] Symptoms Clenched hands Crossed legs (preferred position) Feet with a rounded bottom (rocker-bottom feet) Low birth weight Low-set ears Mental deficiency Small head ( microcephaly[]

    Missing: Absent Pulp Chambers

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