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20 Possible Causes for Broad Nose (12%)

Did you mean: Broad Nose (12, )

  • Cleft Palate

    Sparse and kinky hair with small, carious teeth, and broad nose and a prominent chin gave a typical facial appearance to our patient, similar to cases of Brill et al .[ 12[ncbi.nlm.nih.gov]

  • Central Diabetes Insipidus

    Shortened nose [ more ] 0003196 Wide nose Broad nose Increased breadth of nose Increased nasal breadth Increased nasal width Increased width of nose [ more ] 0000445 Showing[rarediseases.info.nih.gov] […] of 25 Last updated: 12/1/2018 The resources below provide information about treatment options for this condition.[rarediseases.info.nih.gov] […] inheritance 0000006 Gliosis 0002171 Hypertelorism Wide-set eyes Widely spaced eyes [ more ] 0000316 Long philtrum 0000343 Osteopenia 0000938 Short nose Decreased length of nose[rarediseases.info.nih.gov]

  • Ulnar Mammary Syndrome

    People with UMS may have distinct facial features, including a wide face tapering to a prominent chin, and a broad nose. It has been associated with TBX3.[en.wikipedia.org] This gene is located on the long arm of chromosome 12 (12q24.21). Another gene that has been associated with this condition is SYNM.[en.wikipedia.org]

  • Autosomal Dominant Mental Retardation 28

    ] The phenotype is dominated by prenatal and postnatal growth delay, a facial appearance of ʺGreek warrior helmet ʺ with microcephaly, high forehead, broad bridge of the[intechopen.com] A combination of Chromosomal microarray (CMA), FISH, and/or G-banded cytogenetic studies may be necessary for complete characterization of the chromosomerearrangement. [ 12[intechopen.com] nose continuing to the forehead, hypertelorism, epicanthus, highly arched eyebrows, short philtrum, downturned mouth, micrognathia, and poorly formed ears, congenital heart[intechopen.com]

  • Malpuech Syndrome

    Dysmorphic facial features included hypertelorism, upslanting palpebral fissures, broad nasal bridge , short nose, long philtrum, tented upper lip, full cheeks, and large[findzebra.com] Four patients developed seizures between ages 18 months and 12 years; 3 had generalized seizures and 1 had myoclonic seizures.[findzebra.com]

  • Autosomal Dominant Mental Retardation 21

    ] The phenotype is dominated by prenatal and postnatal growth delay, a facial appearance of ʺGreek warrior helmet ʺ with microcephaly, high forehead, broad bridge of the[intechopen.com] A combination of Chromosomal microarray (CMA), FISH, and/or G-banded cytogenetic studies may be necessary for complete characterization of the chromosomerearrangement. [ 12[intechopen.com] nose continuing to the forehead, hypertelorism, epicanthus, highly arched eyebrows, short philtrum, downturned mouth, micrognathia, and poorly formed ears, congenital heart[intechopen.com]

  • Autosomal Dominant Hyper-IgE Syndrome

    Facial asymmetry Broad nose Deep-set eye Prominent forehead Immunol Allergy Clin N Am 28(2008) 227-291 India Journal of Dermatology2015 17.[slideshare.net] […] dendritric cells -- reduced generation of induced regulatory T cell SO patient may manifest anaphylaxis and have more allergy compared to healthy Cur Opin Hematol 2015, 22:12[slideshare.net]

  • XXXXY Syndrome

    Increased width of nasal bridge Nasal bridge broad Wide bridge of nose Widened nasal bridge [ more ] 0000431 Showing of 30 Last updated: 12/1/2018 Making a diagnosis for[rarediseases.info.nih.gov] […] nasal bridge Broad nasal bridge Broad nasal root Broadened nasal bridge Increased breadth of bridge of nose Increased breadth of nasal bridge Increased width of bridge of nose[rarediseases.info.nih.gov]

  • Wolf Hirschhorn Syndrome

    She was noted to have microcephaly, a broad forehead with a prominent glabella, broad nose with a prominent nasal bridge and a short philtrum.[academic.oup.com] Materials and Methods Cell lines Cell line CM was derived from a WHS patient previously described in detail ( 12 ).[academic.oup.com]

  • Trisomy 10p

    Patients have a distinct phenotype consisting of growth and psychomotor retardation, a broad nose, dysplastic low-set ears, micrognathia, congenital heart disease and patchy[plasticsurgerykey.com] Other examples of hyperpigmentation in chromosomal mosaicism are mosaic trisomy 14 and mosaic trisomy 12.[plasticsurgerykey.com] The pattern of pigmentation is similar in mosaic trisomy 12 but the general phenotype is poorly defined [60].[plasticsurgerykey.com]

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