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Results 1 - 7 of 7 for Narrow nasal base
  1. Kaufman oculocerebrofacial syndrome 
    ... in front of the ear (preauricular tags). The nose has a narrow bridge, a wide base, and nostrils that open to the front rather than downward (anteverted nares). Affected individuals may also have flat cheeks; a space between the nose and upper lip (philtrum) that is unusually long ...
    https://medlineplus.gov/.../kaufman-oculocerebrofacial-syndrome - Genetics
  2. CUL3-related neurodevelopmental disorder 
    ... shaped face; a large forehead; a large, rounded nose; small ears; deep-set ... of the muscle at the base of the thumb (thenar hypoplasia), or a single ...
    https://medlineplus.gov/.../cul3-related-neurodevelopmental-disorder - Genetics
  3. 3q29 microdeletion syndrome 
    ... facial features, including a long, narrow face; a narrow space between the nose and upper lip (short philtrum); a high bridge of the nose; and large ears. ... are missing about 1.6 million DNA building blocks (base pairs), also written as 1.6 megabases (Mb), ...
    https://medlineplus.gov/.../condition/3q29-microdeletion-syndrome - Genetics
  4. Potocki-Shaffer syndrome 
    ... wide, short skull (brachycephaly); a prominent forehead; a narrow bridge of the nose; a shortened distance between the nose and upper ...
    https://medlineplus.gov/genetics/condition/potocki-shaffer-syndrome - Genetics
  5. Renpenning syndrome 
    ... features characteristic of this disorder include a long, narrow face; outside corners of the eyes that point upward (upslanting palpebral fissures); a long, bulbous nose with a low-hanging separation between the nostrils ( ...
    https://medlineplus.gov/genetics/condition/renpenning-syndrome - Genetics
  6. 15q24 microdeletion 
    ... long, smooth space between the upper lip and nose (philtrum). This condition is very rare; only a few dozen affected individuals have been identified. People with a 15q24 microdeletion are missing between 1.7 million and 6.1 million DNA building blocks (base pairs), also written as 1.7-6.1 ...
    https://medlineplus.gov/genetics/condition/15q24-microdeletion - Genetics
  7. SLC26A2 gene 
    ... extremely short limbs, short fingers and toes, a narrow chest, and a prominent, rounded abdomen. Serious health ... The other mutation deletes three DNA building blocks (base pairs) at a specific place in the SLC26A2 ...
    https://medlineplus.gov/genetics/gene/slc26a2 - Genetics