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Results 11 - 20 of 143 for Lip disorder
  1. Blepharocheilodontic syndrome 
    ... or palate Elschnig syndrome Lagophthalmia with bilateral cleft lip and palate ... BLEPHAROCHEILODONTIC SYNDROME 1; BCDS1 BLEPHAROCHEILODONTIC SYNDROME 2; ...
    https://medlineplus.gov/.../condition/blepharocheilodontic-syndrome - Genetics
  2. Vici syndrome 
    ... Dionisi-Vici-Sabetta-Gambarara syndrome Immunodeficiency with cleft lip/palate, cataract, hypopigmentation and absent corpus callosum Genetic Testing Registry: Vici syndrome Vici syndrome National Organization for Rare Disorders (NORD) VICI SYNDROME; VICIS PubMed Byrne S, Dionisi- ...
    https://medlineplus.gov/genetics/condition/vici-syndrome - Genetics
  3. Branchio-oculo-facial syndrome 
    ... premature aging Hemangiomatous branchial clefts-lip pseudocleft syndrome Lip pseudocleft-hemagiomatous branchial cyst syndrome ... PubMed Developmental Biology (sixth ...
    https://medlineplus.gov/.../condition/branchio-oculo-facial-syndrome - Genetics
  4. SETBP1 haploinsufficiency disorder 
    ... broad tip of the nose, a thin upper lip, a high arch in the roof of the mouth (high-arched palate), and a small chin. The exact prevalence of SETBP1 haploinsufficiency disorder is unknown, although it is thought to be ...
    https://medlineplus.gov/.../setbp1-haploinsufficiency-disorder - Genetics
  5. PMM2-congenital disorder of glycosylation 
    ... triangular face, large ears, and a thin upper lip. Children with PMM2-CDG may also have elevated liver function test results, seizures, fluid around the heart (pericardial effusion), and blood clotting disorders. About 20 percent of affected infants do not ...
    https://medlineplus.gov/...pmm2-congenital-disorder-of-glycosylation - Genetics
  6. Carney complex 
    ... the body but tend to occur around the lips, eyes, or genitalia. In addition, some affected individuals have at least one blue-black mole called a blue nevus. Carney complex is a rare disorder; fewer than 750 affected individuals have been identified. ...
    https://medlineplus.gov/genetics/condition/carney-complex - Genetics
  7. Xia-Gibbs syndrome 
    ... bridge of the nose, or a thin upper lip. Other, less-common abnormalities involving the bones and skin include premature fusion of certain skull bones (craniosynostosis), unusually loose (lax) joints, and loose skin.Neurodevelopmental disorders can also occur in Xia-Gibbs syndrome. Some ...
    https://medlineplus.gov/genetics/condition/xia-gibbs-syndrome - Genetics
  8. 2q37 deletion syndrome 
    ... thin lips, a smooth space between the upper lip and nose (smooth philtrum), prominent cheekbones, a large chin, and minor ear abnormalities.Other features of 2q37 deletion syndrome can include seizures and an inflammatory skin disorder called eczema. Some affected individuals have malformations of ...
    https://medlineplus.gov/genetics/condition/2q37-deletion-syndrome - Genetics
  9. CDKL5 deficiency disorder 
    ... between the nose and upper lip (philtrum), full lips, widely spaced teeth, and a ... deficiency disorder was previously classified as an atypical form of ...
    https://medlineplus.gov/genetics/condition/cdkl5-deficiency-disorder - Genetics
  10. Kaufman oculocerebrofacial syndrome 
    ... cheeks; a space between the nose and upper lip (philtrum) that is unusually long and smooth; a narrow mouth; and an unusually small jaw (micrognathia).Other signs and symptoms that can occur in people with this disorder include short stature; hearing loss; and abnormalities of ...
    https://medlineplus.gov/.../kaufman-oculocerebrofacial-syndrome - Genetics
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