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Cleft chins are common among people originating from Europe, the Middle East and South Asia. [21] There is a possible genetic cause for cleft chins, a genetic marker called rs11684042, which is located in chromosome 2. [22] In Persian literature, the chin dimple is considered a factor of beauty and is metaphorically referred to as "the chin pit ...
Treacher Collins syndrome (TCS) is a genetic disorder characterized by deformities of the ears, eyes, cheekbones, and chin. [5] The degree to which a person is affected, however, may vary from mild to severe. [5] Complications may include breathing problems, problems seeing, cleft palate, and hearing loss. [5]
Cleft chin: Smooth chin [13] Freckles: No freckles [7] [14] Wet-type earwax: Dry-type earwax [10] [15] Roman nose: No prominent bridge [16] Marfan syndrome: Average body proportions and connective tissue [17] Huntington's disease: No nerve damage [18] Normal mucous lining Cystic fibrosis [19] Photic sneeze reflex: No light-induced sneeze reflex ...
Van der Woude syndrome is inherited as an autosomal dominant disease caused by a mutation in a single gene with equal distribution between the sexes. The disease has high penetrance at about 96% but the phenotypic expression varies from lower lip pits with cleft lip and cleft palate to no visible abnormalities.
This is an accepted version of this page This is the latest accepted revision, reviewed on 29 August 2024. Small natural indentation in the flesh For other uses, see Dimple (disambiguation). Dimple (Gelasin) Bilateral cheek dimples (as seen on model Miranda Kerr) Anatomical terminology [edit on Wikidata] A dimple, also called a gelasin (from Latin gelasinus, from Ancient Greek ...
A bifid nose (also known as cleft nose) is an uncommon congenital malformation which is characterized by the presence of a cleft between the two nostrils of the nose. [1] It is the result of a disturbance during embryological nose development. [2] It is part of the Tessier classification for craniofacial clefts. [3]
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Medical genetics: Symptoms: Jaw, rib, and palate anomalies ... Cerebro-costo-mandibular syndrome is a very rare genetic disorder which is characterized by jaw/chin ...