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6,304 Possible Causes for Absent Pulp Chambers, Low Set Ears, Pediatric Disorder

  • 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).[symptoma.com] Abstract Smith-Magenis Syndrome (SMS) is a complex, pediatric, neurobehavioral, contiguous gene syndrome ascribed to interstitial microdeletion of chromosome 17, band 11.2[ncbi.nlm.nih.gov] ears, and brachydactyly.[link.springer.com]

  • Turner Syndrome

    The aim of this study was to inventory pediatric otologic disorders in patients with TS at their first ENT consultation in our center.[ncbi.nlm.nih.gov] Other characteristics, like widely spaced nipples or low-set ears, also may lead to a suspicion of Turner syndrome.[web.archive.org] According to the American Academy of Pediatrics, every patient with these genetic disorders should have a postnatal echocardiogram.[ncbi.nlm.nih.gov]

    Missing: Absent Pulp Chambers
  • Patau Syndrome

    Nelson Textbook of Pediatrics. 20th ed. Philadelphia, PA: Elsevier; 2016:chap 81. Madan-Khetapal S, Arnold G. Genetic disorders and dysmorphic conditions.[nlm.nih.gov] It leads to a variety of abnormalities that include mental retardation, microcephaly, low-set ears, eye structural defects, polydactyly, and limb abnormalities The presence[icd9data.com] 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[cytogenx.com]

    Missing: Absent Pulp Chambers
  • CHARGE Syndrome

    She is a specialist in pediatric communication disorders and augmentative communication.[smartspeechtherapy.com] 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[gosh.nhs.uk] Developmental disorders with olfactory abnormalities, developmental lag, heart malformations, external genital malformations.[ncbi.nlm.nih.gov]

    Missing: Absent Pulp Chambers
  • Down Syndrome

    Author information 1 Specialized Medical Center, Department of Pediatric Respiratory Medicine, Sleep Disorders Center, Box 84350, Riyadh 11671, Saudi Arabia.[ncbi.nlm.nih.gov] […] variable from individual to individual and may include mental retardation, retarded growth, flat hypoplastic face with short nose, prominent epicanthic skin folds, small low-set[icd9data.com] Christensen, An Instructive Case of Transient Myeloproliferative Disorder, Clinical Pediatrics, 10.1177/0009922816662460, 56, 3, (288-289), (2016).[doi.org]

    Missing: Absent Pulp Chambers
  • Trisomy 18

    Respiratory rate assessment, neonate Venipuncture, pediatric the disorder, diagnosis, underlying cause, and treatment, including the poor prognosis for the infant and the[quizlet.com] During ultrasonographic examination, we discovered that her fetus had several important abnormalities, including a cystic hygroma, craniofacial defects (low-set ears, broad[ncbi.nlm.nih.gov] 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[web.archive.org]

    Missing: Absent Pulp Chambers
  • Velocardiofacial Syndrome

    Behavior, brain, and genome in genomic disorders: Finding the correspondences. Journal of Developmental and Behavioral Pediatrics, 31 , 602–609.[link.springer.com] These may include small, low-set ears, short width of eye openings (palpebral fissures), hooded eyes, a relatively long face, an enlarged nose tip (bulbous), or a short or[mayoclinic.org] He is Professor of Otolaryngology and Professor of Pediatrics at Upstate.[pluralpublishing.com]

    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[indjos.com] Pediatric disorders of sex development. In: Melmed S, Polonsky KS, Larsen PR, Kronenberg HM, eds. Williams Textbook of Endocrinology. 13th ed.[medlineplus.gov] set ears, small teeth, and small nose).[icd10data.com]

  • Cerebro-Oculo-Facio-Skeletal Syndrome

    Cerebro-oculo-facio-skeletal syndrome (COFS) is a pediatric, genetic, degenerative disorder that involves the brain and the spinal cord.[familydiagnosis.com] She was having microcephaly, micrognathia, micro-ophthalmia, large low set ears, upper lip overhanging the lower lip and congenital contractures.[ncbi.nlm.nih.gov] Symptoms may include large, low-set ears, small eyes, microcephaly (abnormal smallness of the head), micrognathia (abnormal smallness of the jaws), clenched fists, wide-set[ninds.nih.gov]

    Missing: Absent Pulp Chambers
  • Noonan Syndrome

    NS is one of the RASopathies, which are a class of pediatric disorders associated with genes that are members of the mitogen-activated protein kinase (Ras/ MAPK ) pathway.[invitae.com] . - It is difficult to look high in the sky at noon, therefore everything is down in NOONan syndrome- Low set ears, Downslanting eyes, Low posterior hair line, Low levels[medicowesome.com] Signs and Symptoms: Distinctive facial features: widely set eyes, low set ears.[care.com]

    Missing: Absent Pulp Chambers

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