Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 10 of 98 for Hypertelorism
  1. Opitz G/BBB syndrome 
    ... G/BBB syndrome has wide-spaced eyes (ocular hypertelorism). Affected individuals commonly have defects of the voice ... X-linked Opitz G/BBB syndrome typically have hypertelorism as the only sign of the disorder. A ...
    https://medlineplus.gov/genetics/condition/opitz-g-bbb-syndrome - Genetics
  2. Baraitser-Winter syndrome 
    ... Distinctive facial features can include widely spaced eyes (hypertelorism), large eyelid openings, droopy eyelids (ptosis), high-arched ... 3 Fryns-Aftimos syndrome Iris coloboma with ptosis, hypertelorism, and mental retardation Genetic Testing Registry: Baraitser-Winter ...
    https://medlineplus.gov/genetics/condition/baraitser-winter-syndrome - Genetics
  3. Hartsfield syndrome 
    ... facial features, including eyes that are widely spaced (hypertelorism) or closely spaced (hypotelorism), ears that are abnormally ... Holoprosencephaly, ectrodactyly, and bilateral cleft lip/palate Holoprosencephaly, hypertelorism, and ectrodactyly syndrome Genetic Testing Registry: Hartsfield-Bixler- ...
    https://medlineplus.gov/genetics/condition/hartsfield-syndrome - Genetics
  4. Donnai-Barrow syndrome 
    ... hernia-exomphalos-corpus callosum agenesis Diaphragmatic hernia-exomphalos-hypertelorism syndrome Faciooculoacousticorenal syndrome FOAR syndrome Genetic Testing Registry: ...
    https://medlineplus.gov/genetics/condition/donnai-barrow-syndrome - Genetics
  5. Wolf-Hirschhorn syndrome 
    Wolf-Hirschhorn syndrome is a condition that affects many parts of the body. The major features of this disorder include a characteristic facial features, ...
    https://medlineplus.gov/genetics/condition/wolf-hirschhorn-syndrome - Genetics
  6. Pfeiffer syndrome 
    Pfeiffer syndrome is a genetic disorder characterized by the premature fusion of certain skull bones (craniosynostosis). This early fusion prevents the skull from ...
    https://medlineplus.gov/genetics/condition/pfeiffer-syndrome - Genetics
  7. Mowat-Wilson syndrome 
    Mowat-Wilson syndrome is a genetic condition that affects many parts of the body. Major signs of this disorder frequently include distinctive facial features, ...
    https://medlineplus.gov/genetics/condition/mowat-wilson-syndrome - Genetics
  8. Frontonasal dysplasia 
    ... of the following features: widely spaced eyes (ocular hypertelorism); a broad nose; a slit (cleft) in one ... facial structures, leading to anterior cranium bifidum occultum, hypertelorism, and other features of frontonasal dysplasia. ALX1 ALX3 ...
    https://medlineplus.gov/genetics/condition/frontonasal-dysplasia - Genetics
  9. Noonan syndrome with multiple lentigines 
    ... to freckles, heart defects, widely spaced eyes (ocular hypertelorism), a sunken chest (pectus excavatum) or protruding chest ( ... a distinctive facial appearance. In addition to ocular hypertelorism, affected individuals may have droopy eyelids (ptosis), thick ...
    https://medlineplus.gov/.../noonan-syndrome-with-multiple-lentigines - Genetics
  10. Aarskog-Scott syndrome 
    ... distinctive facial features, such as widely spaced eyes (hypertelorism), a small nose, a long area between the ... show mild signs of the condition, such as hypertelorism, short stature, or a widow's peak hairline. ...
    https://medlineplus.gov/genetics/condition/aarskog-scott-syndrome - Genetics
previous · 1 · 2 · 3 · 4 · 5 · 6 · 7 · 8 · 9 · 10 · next