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29 Possible Causes for Bifid Tip of Nose

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  • Craniofrontonasal Dysplasia

    Main features of this condition include widely spaced eyes ( hypertelorism ), bifid tip of the nose, broad head (brachycephaly), prominent forehead ( frontal bossing ), asymmetry[rarediseases.info.nih.gov] Zone of the nose Nearly, all patients (91%, n 21) displayed a bifid tip of the nose.[nature.com] Frequently observed phenotypic features were bifid tip of the nose (91%), columellar indentation (91%) and low implantation of breasts (90%).[nature.com]

  • Mohr Syndrome

    Additionally, Mohr syndrome is marked by dysmorphic faces such as a broad nose accompanied by a bifid tip.[symptoma.com] Differentiating feature is broad nose with a bifid tip which is seen in OFD II and hypoplasia of ala nasi which is present in OFD I. [7].[journalofpediatriccriticalcare.com] However, a broad nose with a bifid tip is seen in OFD II instead of the alar hypoplasia which characterizes OFD I. [8] The bilateral hallux, polysyndactyly when present is[jomfp.in]

  • Bifid Nose

    The presentation of a bifid nose ranges from a minimally noticeable midline nasal tip central groove to a complete clefting of the osteocartilaginous framework, resulting[ncbi.nlm.nih.gov] What I see is that the tip of your nose has the classic bifid tip deformity.[eppleyplasticsurgery.com] OR Snapshots – The Bifid Nasal Tip Rhinoplasty The shape of the nose amongst people is as different as that of fingerprints.[exploreplasticsurgery.com]

  • Frontonasal Dysplasia

    Frontonasal dysplasia is defined as hypertelorism, telecanthus and broad bridge of the nose with absent or bifid tip of the nose.[ncbi.nlm.nih.gov] Frontonasal dysplasia (FND) is a genetically heterogeneous malformation spectrum with marked hypertelorism, broad nasal tip and bifid nose.[ncbi.nlm.nih.gov] Among the abnormalities characterised with this disorder were ocular hypertelorism, broad nose tip with median notch, median facial cleft, bifid anterior skull, low set hairline[ncbi.nlm.nih.gov]

  • Familial Isolated Trichomegaly

    tip / cleft nose / supernumerary nose - Blepharitis / eyelid inflammation - Chronic / relapsing otitis - Clinodactyly of fifth finger - Depressed nasal bridge - Epicanthic[csbg.cnb.csic.es] […] logorrhea / dysprosodia Occasional - Abnormal dentition / dental position / implantation / unerupted / dental ankylosis - Atrial septal defect / interauricular communication - Bifid[csbg.cnb.csic.es]

  • Absence or Deformity of Leg- Cataract Syndrome

    bifid tip Thin lips Long philtrum Low set ears Anteverted / prominent / bat ears Sprengel anomaly Inguinal hernia Scoliosis Limb deficiency - ray Bony restriction of joint[mediscansystems.org] […] hemihypertrophy / hemiatrophy Short stature - prenatal / intrauterine dwarfism Short stature - postnatal Short limbs Skin dimples Pointed chin Depressed nasal bridge Cleft nose[mediscansystems.org]

  • Malpuech Syndrome

    Prominent coccyx/caudal appendage Mental retardation Postnatal growth deficiency Telecanthus Bifid tip of the nose Dysplastic/low set ears Down-turned corners of the mouth[documents.tips]

  • Femoral Agenesis - Femoral Hypoplasia

    bifid tip Thin lips Long philtrum Low set ears Anteverted / prominent / bat ears Sprengel anomaly Inguinal hernia Scoliosis Limb deficiency - ray Bony restriction of joint[mediscansystems.org] […] hemihypertrophy / hemiatrophy Short stature - prenatal / intrauterine dwarfism Short stature - postnatal Short limbs Skin dimples Pointed chin Depressed nasal bridge Cleft nose[mediscansystems.org]

  • Femoral Hypoplasia

    bifid tip Thin lips Long philtrum Low set ears Anteverted / prominent / bat ears Sprengel anomaly Inguinal hernia Scoliosis Limb deficiency - ray Bony restriction of joint[mediscansystems.org] […] hemihypertrophy / hemiatrophy Short stature - prenatal / intrauterine dwarfism Short stature - postnatal Short limbs Skin dimples Pointed chin Depressed nasal bridge Cleft nose[mediscansystems.org]

  • Oculocerebral Dysplasia

    In the family they studied, 10 persons had a bifid nasal tip. Of these, 8 had ptosis and 2 scoliosis. Of 3 males, 2 had cryptorchidism.[findzebra.com] Miles and Smith (1985) insisted that the dominant bifid nose syndrome is a distinct entity without ocular hypertelorism.[findzebra.com] Inheritance Anyane-Yeboa et al. (1984) stated that the bifid nose in this family was most likely an autosomal dominant trait. A recessive form (210400) may exist.[findzebra.com]

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