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1,678 Possible Causes for Absent Pulp Chambers, Accentuated Palmar Creases, 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[]

    Missing: Accentuated Palmar Creases
  • Spondyloepimetaphyseal Dysplasia - Abnormal Dentition

    Another related syndrome "familial otodentodysplasia" is characterized by the posterior teeth with abnormal morphology, large pulp chambers, short root length compared to[] Her ears were low set and her hair was normal (Figure 1A).[] […] crown height, and the absent or small premolars in association with high frequency hearing loss. [20] Short Roots Associated with Short Stature but No Syndrome Generalized[]

  • Fetal Hydantoin Syndrome

    Many other findings in fetal alcohol syndrome have been reported, including epican-thic folds, ptosis, hypoplastic maxilla, deep or accentuated palmar creases, and clinodactyly[] The characteristics associated with fetal hydantoin syndrome include distinct facial features, such as low-set ears, widely-spaced eyes, short nose, short neck, and a fold[] Some of the most frequently seen physical deformities include a cleft lip or palate, low-set ears, or a broad nasal bridge.[]

    Missing: Absent Pulp Chambers
  • X-Linked Mandibulofacial Dysostosis

    chambers, Pulp obliteration occurs after eruption, Roots of permanent and primary teeth are normal shape and length, Permanent teeth - pulp chambers are abnormally large,[] ears Low set ears Lowset ears [ more ] 0000369 Specific learning disability 0001328 X-linked inheritance 0001417 Showing of 29 Last updated: 5/1/2019 If you need medical[] UNK DiGeorge syndrome chromosome region CATCH22 22q11 188400 DiGeorge syndrome 188400 AD low-set ears, short ears, small mouth, submucous or overt palatal cleft, cleft lip[]

    Missing: Accentuated Palmar Creases
  • 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 Accentuated Palmar Creases
  • Hallermann-Streiff Syndrome

    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[] ears Low set ears Lowset ears [ more ] 0000369 Metaphyseal widening Broad wide portion of long bone 0003016 Narrow nose Decreased nasal breadth Decreased nasal width Thin[]

    Missing: Absent Pulp Chambers Accentuated Palmar Creases
  • Patterson Pseudoleprechaunism Syndrome

    […] and palmar skin creases.[] Elfin facies, Protuberant ears, Low-set ears, Poorly developed ears, Flat nasal bridge, Flared nostrils, Thick lips, Macrostomia, Microcephaly, Hypertelorism, High arched[] set ears; autosomal recessive inheritance; caused by mutat … Medical dictionary Donohue syndrome — Classification and external resources insulin receptor OMIM 246200 … Wikipedia[]

    Missing: Absent Pulp Chambers
  • Mandibulofacial Dysostosis

    An exam of the infant may reveal a variety of problems, including: Abnormal eye shape Flat cheekbones Cleft palate or lip Small jaw Low-set ears Abnormally formed ears Abnormal[]

    Missing: Absent Pulp Chambers Accentuated Palmar Creases
  • Patau Syndrome

    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[] Other birth defects of trisomy 13 include: Clenched hands Cleft lip or palate Extra fingers or toes (polydactyly) Hernias Kidney, wrist, or scalp problems Low-set ears Small[]

    Missing: Absent Pulp Chambers Accentuated Palmar Creases
  • 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 Accentuated Palmar Creases

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