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1,208 Possible Causes for long, Narrow Face

  • Sinusitis

    Your doctor may order a MRI or CT scan to look for abnormalities in the sinuses – narrow drainage passages, polyps or a deviated septum.[aaaai.org] Treatment included long-term antifungal therapy and conservative endoscopic surgery in all but 1 patient, who had an open approach.[ncbi.nlm.nih.gov] The patient was managed with conservative surgery and long-term oral voriconazole.[ncbi.nlm.nih.gov]

  • Infectious Mononucleosis

    The tonsils are usually enlarged and the upper airway passageway may appear narrowed. Petechiae on the soft palate are also common.[symptoma.com] The way mono works in the body is tricky, so lots of people are confused about how long it is contagious.[web.archive.org] Health experts aren't sure how long people with mono stay contagious after symptoms are gone.[kidshealth.org]

  • Acromegaly

    […] which causes narrowing of the bony frame work of the nasopahrynx.[omicsonline.org] Addition of pegvisomant (PEGV), a GH receptor antagonist, could improve this; however, the literature has not described long-term follow-up.[ncbi.nlm.nih.gov] In addition to a puffy and "fuller" face, Meer's ring size has gone from a 7 to a 9 1/2 and her feet from 7 1/2 narrow to 9 1/2 medium.[web.archive.org]

  • Kaufman Oculocerebrofacial Syndrome

    Kaufman oculocerebrofacial syndrome (KOS) is a rare autosomal recessive disorder characterized by severe mental retardation, microcephaly, long narrow face, ocular anomalies[ncbi.nlm.nih.gov] face, eye anomalies, small mandible, upslanting palpebral fissure (the distance between the upper & lower eyelids), highly arched palates & preauricular skin tags. severely[signssymptoms.org] […] anomalies, and long thin hands and feet.[doi.org]

  • Bloom Syndrome

    Bloom syndrome - congenital telangiectatic erythema and dwarfism with normal body proportions except for a narrow face and dolichocephalic skull.[medical-dictionary.thefreedictionary.com] Bloom Syndrome by Long Le Bloom syndrome is a rare autosomal recessive genetic disease that features an elevated rate of sister chromatid exchange.[www-personal.umd.umich.edu] To accomplish this, we tested a catalytically active WRN helicase domain fragment (WRN(H-R)) that lacked the N-terminal RPA interaction site for its ability to unwind long[ncbi.nlm.nih.gov]

  • FRAXA Syndrome

    .  Large testes (Macroorchidism)  Large ears  Long, narrow face  Soft skin  Poor eyesight  Large body size  Square chin  Frontal bossing 7.[slideshare.net] We hypothesize that this subgroup of alleles and haplotypes are associated with long pure CGGs ( 15 CGG) or 35 repeats and, having shared an evolutionary past, would have[ncbi.nlm.nih.gov] More subtle physical symptoms can include a long, narrow face with prominent ears, joint laxity and flat feet.[spectrumnews.org]

  • Autosomal Recessive Mental Retardation 5

    : smooth philtrum short philtrum narrow face long face small chin Muscle Soft Tissue: hypertonia distal myopathy (in 1 family) Growth Weight: postnatal growth retardation[malacards.org] […] and narrow face, bushy eyebrows with synophrys, hypotelorism, large nose with long columella, short philtrum, and full upper lip.[cags.org.ae] PreventionGenetics also offers DNA Banking (PGDNABank), a long-term storage of a person’s DNA. DNA Banking is available direct-to-consumer.[preventiongenetics.com]

  • Marfan Syndrome

    […] view 613 KB version view 3 KB version A young man with Marfan syndrome, showing characteristically long limbs and narrow face. view 369 KB version view 5 KB version Arachnodactyly[medgen.genetics.utah.edu] The main clinical manifestations include long limbs, long slender fingers, lens subluxation, abnormal cardiac valves, and aortic aneurysm.[ncbi.nlm.nih.gov] face Many people with Marfan syndrome suffer from chronic muscle and joint pain.[nlm.nih.gov]

  • Seckel Syndrome

    Small head, large eyes, beak-like nose, narrow face, and receding mandible. Laryngeal stenosis.[accessanesthesiology.mhmedical.com] Analysis of bone marrow chromosomes showed an abnormal clone with abnormalities involving multiple chromosomes, including monosomy 7, trisomy 8, trisomy 11, and loss of the long[ncbi.nlm.nih.gov] Long-term GH treatment of the youngest brother and sister increased the FH by 7.2 and 3.4 cm, respectively, compared with their older brother and sister.[ncbi.nlm.nih.gov]

  • Ehlers Danlos Syndrome Beasley Cohen Type

    : narrow face Head And Neck Ears: hearing loss Head And Neck Eyes: cataracts small eyes Clinical features from OMIM: 608763 Human phenotypes related to Ehlers-Danlos Syndrome[malacards.org] Other common features include a "marfanoid habitus" which is characterized by long, slender fingers (arachnodactyly); unusually long limbs; and a sunken chest (pectus excavatum[en.scio.pw] […] rheumatoid patients (whether by prednisone or longer term drugs such as penicillamine or gold) must be considered abnormal-as hypermobility for that patient which in the long[books.google.de]

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