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444 Possible Causes for Broad Nasal Bridge, Epicanthal Folds, Low Set Ears

  • Homocystinuria

    The patient also shows signs that had not been previously described: epicanthal folds, broad nasal bridge, long and flat philtrum, amimic expression and, particularly, a postural[] The patient also shows signs that had not been previously described: epicanthal folds, broad nasal bridge, long and flat philtrum, amimic expression and, particularly, a postural[] The patient shows some of the facial features that were already reported in the literature (high forehead, large floppy, low-set ears, flat philtrum and hypotonia of perioral[]

  • Down Syndrome

    folds, flattened nasal bridge, broad hands with short fingers, decreased muscle tone, and by trisomy of the human chromosome numbered 21 — called also Down , Down's , trisomy[] […] syndrome there is a level of cognitive impairment, as well as the characteristic craniofacial features, such as an anteriorly and posteriorly flattened head, dysplastic low-set[] In the postnatal period, characteristic phenotypical features point to the diagnosis: depressed nasal bridge epicanthic folds abundant neck skin macroglossia simian crease[]

  • Smith-Magenis Syndrome

    folds, broad nasal bridge, downturned mouth with cupid's bow, ear anomalies, and relative prognathism, and ocular abnormalities); short stature; brachydactyly; a hoarse,[] 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,[] ears, and brachydactyly.[]

  • Pallister-Killian Syndrome

    These abnormalities included webbed neck, low-set ears, lower jaw tooth bud, left simian crease, shield chest, focal aplasia cutis, diaphragmatic hernia, hypoplastic lungs[] folds large ears with lobes that are thick and protrude outward.[] 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[]

  • Rubinstein-Taybi Syndrome

    […] syn·drome ( rū'bĭn-stīn tā'bē ), mental retardation, broad thumb and great toe, antimongoloid slant to the eyes, thin and beaked nose, microcephaly, prominent forehead, low-set[] […] of skin on either side of the nose that may cover the eyes’ inner corners (epicanthal folds).[] Extra oral features revealed distinctive facial appearance with a broad fore head, hypertelorism, broad nasal bridge and beaked nose.[]

  • Aarskog Syndrome

    Sporadic Symptoms Round face and a shorter neck, epicanthic folds, maxillary hypoplasia, which causes several facial abnormalities, and single transverse palmar crease may[] The major facial manifestations of this syndrome include hypertelorism, broad forehead, broad nasal bridge, short nose with anteverted nostrils, long philtrum, widow's peak[] Low-set ears and thickened, fleshy earlobes. Delayed eruption of teeth Underdevelopment of the hard outer covering of teeth (enamel hypoplasia).[]

  • Cri Du Chat Syndrome

    Among the consequent abnormalities are low birth weight, a striking catlike cry in infancy, mental retardation, epicanthal folds, hypertelorism and dental malocclusions.[] nasal bridge, downward slanting palpebral fissures, and micrognathia.[] set ears and short IV metacarpals has not changed with advancing age.[]

  • Trigonocephaly

    Both children showed the pattern of abnormal findings characteristic of this syndrome, including trigonocephaly, upslanted palpebral fissures, inner epicanthic folds, broad[] We describe 2 children with severe ptosis, trigonocephaly, broad nasal bridge, and major brain malformation.[] We report on a patient with trigonocephaly, biparietal widening as a result of metopic synostosis, strabismus, upslanted palpebral fissures, apparently low-set ears with abnormal[]

  • Neonatal Adrenoleukodystrophy

    Polar cataracts, strabismus, and epicanthal folds have also been reported.[] The clinical findings of the ZS are dysmorphic features (prominent forehead, hypertelorism, epicanthal folds, flat supraorbital ridges, broad nasal bridge, large fontanelles[] Facial dysmorphism (50%) with hypertelorism, epicanthus, low nasal bridge, and low-set ears may be present. Some children have polydactyly and hepatomegaly.[]

  • Ring Chromosome 4

    The fetus postnatally manifested hypertelorism, epicanthic folds, a prominent nose, a triangular face, low-set ears, clinodactyly of the fingers, and small big toes.[] The remainder of physical examination revealed curly hair, thin upper lip, broad nasal bridge and tip.[] folds * Highly arched palate * Cleft palate * Tooth enamel hypoplasia * Clinodactyly * Thumb aplasia * Thumb hypoplasia * Abnormal palmar creases * Hip dislocation * Radial[]

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