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174 Possible Causes for Bitemporal Narrowing

  • Hunter-MacDonald Syndrome

    […] pulmonary valves Impaired hearing Disproportionate short stature Congenital camptodactyly Scoliosis Epiphyseal dysplasia Early osteoarthritis Malformed feet Bitemporal narrowing[] Craniofacial manifestations include normal head circumference, tall forehead, bitemporal narrowing, ptosis, short palpebral fissures, and short philtrum.[] * Partially dislocated thumbs * Malformed feet * Tall forehead * Bitemporal narrowing * Droopy eyelids * Short eye slits * Short upper lip groove * Reduced hearing acuity[]

  • 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[] narrowing: The size of the head above the eyes are narrow Microcephaly (small head) Feeding problems Difficulty to grow and thrive Syndactyly or fused toes; polydactyly or[] […] palate or split upper lip Micrognathia or small size of the jaws Broad nose, flat nasal bridge Nostrils flaring upwards Ptosis or drooping of the upper or lower eyelids Bitemporal[]

  • 2p16.1-P15 Deletion Syndrome

    narrowing, smooth and long philtrum, hypertelorism, downslanting palpebral fissures, broad nasal root, thin upper lip, and high palate.[] Dysmorphic features: bitemporal narrowing, receding short forehead, metopic prominence or craniosynostosis, abnormal head shape, epicanthal folds, short palpebral fissures[] […] neurodevelopmental disorder characterized by delayed psychomotor development, intellectual disability, and variable but distinctive dysmorphic features, including microcephaly, 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[] narrowing, depressed nasal bridge, and micrognathia; Patient 3 had early global developmental delay with later progressive spastic quadriparesis, intellectual disability,[] […] previous reports Patients 1 and 2 (full siblings) have severe global developmental delay, gastroesophageal reflux disease, and minor dysmorphic features, including high palate, bitemporal[]

  • Cerebro-Facio-Articular Syndrome

    Craniofacial dysmorphism included a wide anterior fontanelle, bitemporal narrowing, short upslanting palpebral fissures with mild ptosis, prominent eyes, strabismus, thickened[] Hypotonia and facial dysmorphism were noted from birth with bitemporal narrowing, flat supra-orbital ridges, epicanthic folds, blepharophimosis, a small mouth and small undermodelled[]

  • Verheij Syndrome

    forehead IEA IEA OMIM-CS:HEAD AND NECK_FACE BITEMPORAL NARROWING OMIM:615583 HPO:skoehler 06.02.2014 OMIM:615583 #615583 VERHEIJ SYNDROME; VRJS;;CHROMOSOME 8q24.3 DELETION[] The facial phenotype developed with a broad forehead, bitemporal narrowing, low nasal root, periorbital fullness, full cheeks and lips and wide opened mouth.[] IEA IEA OMIM-CS:HEAD AND NECK_EYES COLOBOMA OMIM:615583 HPO:skoehler 06.02.2014 OMIM:615583 #615583 VERHEIJ SYNDROME; VRJS;;CHROMOSOME 8q24.3 DELETION SYNDROME HP:0000341 Narrow[]

  • Carpenter-Waziri Syndrome

    Facial asymmetry, bitemporal narrowing, and small teeth with irregular placement may be present. Ear size and architecture is not remarkable.[] narrowness, almond-shaped palpebral fissures, depressed nasal bridge, anteverted nares, short and inverted-V-shaped upper lip, and macrostomia.[] […] maternal uncles with moderate to severe mental retardation, short stature, mild obesity, hypogonadism, a low total finger ridge count, and a distinctive face characterized by bitemporal[]

  • Autosomal Recessive Primary Microcephaly 4

    Minor dysmorphic features (Fig. 1) were noted including bitemporal narrowing, prominent eyes, upturned nostrils, long philtrum, micro-retrognathia and a short neck. …[]

  • Papillomas in Perioral, Nasal and Anal Regions

    narrowing, shallow orbits, lack of eyebrows and/or eyelashes, webbed neck, low set ears, hypertelorism, coarse facies), developmental delay, seizures, poor growth and feeding[] […] dermatologic abnormalities (sparse or curly hair, atopic dermatitis keratosis pilaris, ichthyosis), dysmorphic facial features (macrocephaly with broad forehead,spurs curly hair bitemporal[]

  • Trigonocephaly

    narrowing but overcorrected the rounding of the forehead.[] […] the 3D comparison of forehead shapes of metopic patients and non-craniosynostotic controls, and demonstrated that the adopted FOR technique was successful in correcting bitemporal[]

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