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Results 1 - 10 of 98 for Nasal disorder
  1. Burn-McKeown syndrome 
    Burn-McKeown syndrome is a disorder that is present from birth (congenital) and involves abnormalities of the nasal passages, characteristic facial features, hearing loss, heart abnormalities, and short stature.In people with Burn-McKeown syndrome, both nasal passages are ...
    https://medlineplus.gov/genetics/condition/burn-mckeown-syndrome - Genetics
  2. Zellweger spectrum disorder 
    ... distinctive facial features, including a flattened face, broad nasal bridge, high forehead, and widely spaced eyes (hypertelorism). Children with severe Zellweger spectrum disorder typically do not survive beyond the first year ...
    https://medlineplus.gov/.../condition/zellweger-spectrum-disorder - Genetics
  3. Fumarase deficiency 
    ... widely spaced eyes (ocular hypertelorism), and a depressed nasal bridge. An enlarged liver and spleen (hepatosplenomegaly) may also be associated with this disorder, as well as an excess of red blood ...
    https://medlineplus.gov/genetics/condition/fumarase-deficiency - Genetics
  4. Wolf-Hirschhorn syndrome 
    ... intellectual disability, and seizures.Almost everyone with this disorder has distinctive facial features, including a broad nasal bridge, large and protruding eyes, and a high ...
    https://medlineplus.gov/genetics/condition/wolf-hirschhorn-syndrome - Genetics
  5. Cytochrome P450 oxidoreductase deficiency 
    ... in a bent position. A blockage of the nasal passages (choanal atresia), intellectual disability, and delayed development are also associated with the severe form of the disorder.Some women who are pregnant with fetuses affected ...
    https://medlineplus.gov/...cytochrome-p450-oxidoreductase-deficiency - Genetics
  6. FREM1 gene 
    ... membranes of particular tissues, resulting in the cleft nasal cartilage (bifid nose), missing kidneys (renal agenesis), narrowed or misplaced anal opening (anorectal malformations), and other features characteristic of this disorder. Researchers suggest that BNAR and Manitoba oculotrichoanal syndrome, ...
    https://medlineplus.gov/genetics/gene/frem1 - Genetics
  7. Opitz G/BBB syndrome 
    ... facial features that may be seen in this disorder include a prominent forehead, widow's peak hairline, flat nasal bridge, thin upper lip, and low-set ears. ...
    https://medlineplus.gov/genetics/condition/opitz-g-bbb-syndrome - Genetics
  8. Hereditary neuralgic amyotrophy 
    ... corner of the eye (epicanthal fold), a long nasal bridge, a narrow mouth, and differences between one side of the face and the other (facial asymmetry). Hereditary neuralgic amyotrophy is a rare disorder, but its specific prevalence is unknown. Variants (also ...
    https://medlineplus.gov/.../hereditary-neuralgic-amyotrophy - Genetics
  9. TXNL4A gene 
    ... identified in people with Burn-McKeown syndrome, a disorder that is present from birth (congenital) and involves abnormalities of the nasal passages, characteristic facial features, hearing loss, heart abnormalities, ...
    https://medlineplus.gov/genetics/gene/txnl4a - Genetics
  10. Bosma arhinia microphthalmia syndrome 
    ... syndrome BAMS Bosma syndrome Gifford-Bosma syndrome Hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome Ruprecht Majewski syndrome ... PubMed Brasseur ...
    https://medlineplus.gov/.../bosma-arhinia-microphthalmia-syndrome - Genetics
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