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662 Possible Causes for Narrow Forehead

  • Sinusitis

    Mucus leaving the frontal (forehead) and maxillary (cheek) sinuses drains through the ethmoid sinuses (behind the bridge of the nose), so a backup in the ethmoids is likely[health.harvard.edu] They are located in the cheeks (maxillary), forehead (frontal) and around the eyes (ethmoidal).[betterhealth.vic.gov.au] Anatomy of the paranasal sinuses The paranasal sinuses comprise four pairs of sinuses that surround the nose and drain into the nasal cavity by way of narrow channels called[health.harvard.edu]

  • 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[ncbi.nlm.nih.gov] The characteristic findings are mental retardation, characteristic facies, narrow forehead, bushy eyebrows with synophrys, hypertelorism, broad nose, wide philtrum, triangular-shaped[ncbi.nlm.nih.gov] MorphologicalEpicanthus 2 2 2 2Hypertelorism Broad short nose Short neck Low-set, posteriorlyangulated ears Synophrys 2 2 Flat face Low hairline 2 Narrow forehead ? ?[docslide.com.br]

  • Verheij Syndrome

    forehead Short nose Thin upper lip vermilion Abnormality of limbs Clinodactyly Hip dislocation Short 5th finger Abnormality of the abdomen ... ...[familydiagnosis.com] forehead Decreased width of the forehead 0000341 Renal agenesis Absent kidney Missing kidney [ more ] 0000104 Renal cyst Kidney cyst 0000107 Renal hypoplasia Small kidneys[rarediseases.info.nih.gov] Symptoms of Verheij syndrome Clinical features : Imported from Human Phenotype Ontology (HPO) Abnormality of head or neck Congenital ocular coloboma Long philtrum Microcephaly Narrow[familydiagnosis.com]

  • Smith Lemli Opitz Syndrome

    forehead, hyperthelorism, micrognathia, anteverted nares, ambiguous genitalia, and signs of intrauterine growth restriction.[ncbi.nlm.nih.gov] A characteristic craniofacial pattern profile was universally present: narrow forehead, brachycephaly, short palpebral fissures, short nasal ridge, anteverted nares, flat[ncbi.nlm.nih.gov] The following are the most commonly observed features: Characteristic facial features (narrow forehead, epicanthal folds, ptosis, short mandible with preservation of jaw width[ncbi.nlm.nih.gov]

  • 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[rarediseases.info.nih.gov] , a triangularly shaped head, a narrow forehead and eyes that are positioned close together.[cincinnatichildrens.org] […] 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[rarediseases.info.nih.gov]

  • Carpenter-Waziri Syndrome

    forehead ; Obesity ; Open mouth ; Optic atrophy ; Paroxysmal bursts of laughter ; Pes planus ; Phenotypic variability ; Posteriorly rotated ears ; Protruding tongue ; Ptosis[mousephenotype.org] forehead Spastic tetraplegia Protruding tongue Genu recurvatum Excessive salivation Acetabular dysplasia Everted upper lip vermilion Synophrys Lumbar scoliosis Periventricular[mendelian.co] Individuals affected with sagittal craniosynostosis have narrow, prominent foreheads and the back of the head is much larger than normal.[en.wikipedia.org]

  • Hunter-MacDonald Syndrome

    Craniofacial manifestations include normal head circumference, tall forehead, bitemporal narrowing, ptosis, short palpebral fissures, and short philtrum.[ncbi.nlm.nih.gov] * Partially dislocated thumbs * Malformed feet * Tall forehead * Bitemporal narrowing * Droopy eyelids * Short eye slits * Short upper lip groove * Reduced hearing acuity[checkorphan.org] * Skewed fingers * Delayed bone age * Abnormal bone development * Mitral valve prolapse * Bicuspid aortic valve * Mild mitral regurgitation * Mild aortic regurgitation * Narrowed[checkorphan.org]

  • 2p16.1-P15 Deletion Syndrome

    Clinical examination showed: weight 13 kg, height 98 cm, head circumference 49 cm, neonatal jaundice, dysmorphisms (narrow forehead, epicanthic folds, up-slnated palpebral[cordis.europa.eu] Dysmorphic features: bitemporal narrowing, receding short forehead, metopic prominence or craniosynostosis, abnormal head shape, epicanthal folds, short palpebral fissures[gene.sfari.org] forehead, round face, deep-set eyes, blue sclerae, large and prominent ears, nose with anteverted nares, thin upper lip, small and wide-spaced teeth, hyperextensibility of[cordis.europa.eu]

  • Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 3

    forehead Open mouth Cortical visual impairment Status epilepticus Nephrocalcinosis Calcinosis Deep philtrum And 56 more phenotypes.[mendelian.co] forehead Cryptorchidism Pes planus Neurological speech impairment Impaired pain sensation Hydronephrosis Broad nasal tip Narrow palate Low-set ears Feeding difficulties Gait[mendelian.co] Dysmorphic features included brachycephaly, high forehead with bitemporal narrowing, depressed nasal bridge, long philtrum with a deep groove, and open mouth due to hypotonia[bio2rdf.org]

  • Cerebro-Facio-Articular Syndrome

    We report another case of cerebro-facio-thoracic dysplasia (Pascual-Castroviejo syndrome) characterized by mental retardation and characteristic facies: narrow forehead, synophris[pubfacts.com] The boy had distinct facial dysmorphic features: prominent forehead with a high frontal hairline, telecanthus, bilateral epicanthic folds, narrow palpebral fissures, full cheeks[kundoc.com]

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