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221 Possible Causes for Bitemporal Narrowing

  • Smith Lemli Opitz Syndrome

    Microcephaly (80% of cases), bitemporal narrowing, ptosis, a broad nasal bridge, short nasal root, anteverted nares (90% of cases), a small chin, and micrognathia are common[] forehead, hyperthelorism, micrognathia, anteverted nares, ambiguous genitalia, and signs of intrauterine growth restriction.[] A characteristic craniofacial pattern profile was universally present: narrow forehead, brachycephaly, short palpebral fissures, short nasal ridge, anteverted nares, flat[]

  • Pitt-Hopkins Syndrome

    narrowing, squared forehead, deep-set eyes, peculiar nose conformation, with broad nasal bridge, down-turned nasal tip and flaring nostrils, typical shape of the mouth, with[] […] distinctive of Pitt–Hopkins syndrome are breathing abnormalities, that can occur as either hyperventilation episodes or apnea crises, and a typical facial dysmorphism, including bitemporal[] […] distinctive of Pitt-Hopkins syndrome are breathing abnormalities, that can occur as either hyperventilation episodes or apnea crises, and a typical facial dysmorphism, including bitemporal[]

  • Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 3

    Dysmorphic features included brachycephaly, high forehead with bitemporal narrowing, depressed nasal bridge, long philtrum with a deep groove, and open mouth due to hypotonia[]

  • Pseudoaminopterin Syndrome

    forehead Decreased width of the forehead 0000341 Narrow palpebral fissure Small opening between the eyelids 0045025 Oligodontia Failure of development of more than six teeth[] […] circumference Small head circumference [ more ] 0000252 Micrognathia Little lower jaw Small jaw Small lower jaw [ more ] 0000347 Muscular hypotonia Low or weak muscle tone 0001252 Narrow[]

  • Cerebro-Facio-Thoracic Dysplasia

    Abstract We report another case of cerebro-facio-thoracic dysplasia (Pascual-Castroviejo syndrome) characterized by mental retardation and characteristic facies: narrow forehead[] The characteristic findings are mental retardation, characteristic facies, narrow forehead, bushy eyebrows with synophrys, hypertelorism, broad nose, wide philtrum, triangular-shaped[] MorphologicalEpicanthus 2 2 2 2Hypertelorism Broad short nose Short neck Low-set, posteriorlyangulated ears Synophrys 2 2 Flat face Low hairline 2 Narrow forehead ? ?[]

  • Hypogonadism

    Features include emotional lability, poor gross motor skills, facial abnormalities (eg, a narrow bitemporal dimension, almond-shaped eyes, a mouth with thin upper lips and[]

  • Scoliosis

    forehead.[] Prader-Willi syndrome can be recognized by the presence of certain facial features, including almond-shaped eyes, a thin upper lip, a prominent nasal bridge, and a high, narrow[]

  • Autistic Disorder

    Because of her dysmorphic characteristics comprising narrow face, narrow forehead, mandibular prognathism, synophrys, and operated cleft palate and cardiac problems, she had[]

  • Familial Scaphocephaly Syndrome

    When this suture closes early, the baby begins to have an elongation of the head from front to back (scaphocephaly) with narrowing of the temple region (bitemporal narrowing[] Results and conclusions The newborn had sagittal craniosynostosis (scaphocephaly), microcephaly, facial asymmetry, short forehead and bitemporal narrowing, microtia, hypoplastic[] Both groups have bitemporal narrowing and may have frontal and/or occipital bossing in pronounced cases.[]

  • Multiple Congenital Anomalies

    narrowing, depressed nasal bridge, and micrognathia; Patient 3 had early global developmental delay with later progressive spastic quadriparesis, intellectual disability,[] There was frontal bossing, orbital hypothelorism, bitemporal narrowing, a short and upturned nose, micrognathia, high palatal groove, downturned mouth, and a notched alveolar[] […] previous reports Patients 1 and 2 (full siblings) have severe global developmental delay, gastroesophageal reflux disease, and minor dysmorphic features, including high palate, bitemporal[]

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