2006
DOI: 10.1016/j.ijporl.2005.06.001
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Anthropometric growth study of auricle of healthy preterm and term newborns

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Cited by 26 publications
(20 citation statements)
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“…1 Studies on the age-related variations in ear linear dimensions during growth, development and ageing was reported in some ethnic group especial Caucasian; Dutch, 2 German, 3 Italian, [4][5][6] European, 7 North American, 1,8 Turkish. [9][10][11] Other population include Indian, [12][13][14] Ashkenazi and Sephardi Jew, 15 Japanese, 16 Nigeria. 17 Anomalies of the ear including missing external ear, prominent ears, and microtia may be as a result of various causes such as trauma, surgical resection, tumours, or congenital deformities.…”
Section: Introductionmentioning
confidence: 99%
“…1 Studies on the age-related variations in ear linear dimensions during growth, development and ageing was reported in some ethnic group especial Caucasian; Dutch, 2 German, 3 Italian, [4][5][6] European, 7 North American, 1,8 Turkish. [9][10][11] Other population include Indian, [12][13][14] Ashkenazi and Sephardi Jew, 15 Japanese, 16 Nigeria. 17 Anomalies of the ear including missing external ear, prominent ears, and microtia may be as a result of various causes such as trauma, surgical resection, tumours, or congenital deformities.…”
Section: Introductionmentioning
confidence: 99%
“…Postnatal abnormalities in ear dimensions and position are common findings in several alterations of the human chromosomes and karyotype, and in developmental defects of the first and second branchial archs [3,10,11,[13][14][15][16][17][18][19][20][21]. For instance, in persons with Down's syndrome ear length and width are reduced, the earlobe is often more protruding from head surface, and there is an increased right-left asymmetry [10,11,[13][14][15][16]19,22]. In contrast, wide ears can be found in Apert and Crouzon syndromes [1,10,19].…”
Section: Introductionmentioning
confidence: 99%
“…For instance, in persons with Down's syndrome ear length and width are reduced, the earlobe is often more protruding from head surface, and there is an increased right-left asymmetry [10,11,[13][14][15][16]19,22]. In contrast, wide ears can be found in Apert and Crouzon syndromes [1,10,19]. Low-set ears can be found in persons with Noonan syndrome [17,20], and with trisomy 13 and 18 [10]; prominent ears can be found in Turner syndrome [22].…”
Section: Introductionmentioning
confidence: 99%
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“…Ancak kulak gelişimini çok erken yaşlarda tamamlandığından bu yaş grubu ile erişkin yaş grubu arasında benzer sonuç-lar beklenmektedir. [18] French ve ark. [6] ise retrospektif olarak mastoidektomi uyguladıkları hastaları incelemişler ve aurikulanın cerrahi sonrası inferiora doğru yer değiştirdiğini tespit etmişlerdir.…”
Section: Discussionunclassified