Literature DB >> 8908264

Clinical analysis of 592 patients with microtia.

H Okajima1, Y Takeichi, K Umeda, S Baba.   

Abstract

Clinical and statistical analyses were performed on 592 patients who visited our hospital between April 1968 and March 1995. The preponderance in men (64.7%) and right-side (58.4%) was distinct statistically. The material shows that grade III microtia, peanut-shell type, was the most frequent with 56.8%. It is complicated with congenital stenosis or atresia in most cases (92.0%). The degree of anomalies of the auricle and external auditory meatus was generally interrelated. Ten cases of familial microtia were discovered, and all parent-child cases were father-child. About 27.9% of the patients' mothers had had a cold, threatened abortion, gestosis, anemia, etc during their pregnancy. Except for 6 patients with Treacher-Collin's syndrome and 2 patients whose mothers took thalidomide during pregnancy, we could not demonstrate the cause of the microtia, whether general or environmental.

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Mesh:

Year:  1996        PMID: 8908264

Source DB:  PubMed          Journal:  Acta Otolaryngol Suppl        ISSN: 0365-5237


  10 in total

1.  Sociodemographic, health behavioral, and clinical risk factors for anotia/microtia in a population-based case-control study.

Authors:  Marisa A Ryan; Andrew F Olshan; Mark A Canfield; Adrienne T Hoyt; Angela E Scheuerle; Suzan L Carmichael; Gary M Shaw; Martha M Werler; Sarah C Fisher; Tania A Desrosiers
Journal:  Int J Pediatr Otorhinolaryngol       Date:  2019-03-23       Impact factor: 1.675

Review 2.  Genetic Advances in the Understanding of Microtia.

Authors:  Craig Gendron; Ann Schwentker; John A van Aalst
Journal:  J Pediatr Genet       Date:  2016-09-23

Review 3.  Microtia: epidemiology and genetics.

Authors:  Daniela V Luquetti; Carrie L Heike; Anne V Hing; Michael L Cunningham; Timothy C Cox
Journal:  Am J Med Genet A       Date:  2011-11-21       Impact factor: 2.802

4.  Microtia-anotia: a global review of prevalence rates.

Authors:  Daniela Varela Luquetti; Emanuele Leoncini; Pierpaolo Mastroiacovo
Journal:  Birth Defects Res A Clin Mol Teratol       Date:  2011-06-07

5.  A mutation in HOXA2 is responsible for autosomal-recessive microtia in an Iranian family.

Authors:  Fatemeh Alasti; Abdorrahim Sadeghi; Mohammad Hossein Sanati; Mohammad Farhadi; Elliot Stollar; Thomas Somers; Guy Van Camp
Journal:  Am J Hum Genet       Date:  2008-04       Impact factor: 11.025

6.  Identification of sequence variants associated with severe microtia-astresia by targeted sequencing.

Authors:  Pu Wang; Yibei Wang; Xinmiao Fan; Yaping Liu; Yue Fan; Tao Liu; Chongjian Chen; Shuyang Zhang; Xiaowei Chen
Journal:  BMC Med Genomics       Date:  2019-01-28       Impact factor: 3.063

7.  Microtia: A Data Linkage Study of Epidemiology and Implications for Service Delivery.

Authors:  Thomas H Jovic; John A G Gibson; Rowena Griffiths; Thomas D Dobbs; Ashley Akbari; Nicholas Wilson-Jones; Rhodri Costello; Peter Evans; Mark Cooper; Steve Key; Ronan Lyons; Iain S Whitaker
Journal:  Front Pediatr       Date:  2021-03-26       Impact factor: 3.418

8.  Predicting the Risk of Microtia From Prenatal Factors: A Hospital-Based Case-Control Study.

Authors:  Wei Chen; Manqing Sun; Yue Zhang; Qun Zhang; Xiaolin Xu
Journal:  Front Pediatr       Date:  2022-04-21       Impact factor: 3.418

9.  Target sequencing of 307 deafness genes identifies candidate genes implicated in microtia.

Authors:  Pu Wang; Xinmiao Fan; Yibei Wang; Yue Fan; Yaping Liu; Shuyang Zhang; Xiaowei Chen
Journal:  Oncotarget       Date:  2017-06-28

10.  DNA Methylation Patterns of Chronic Explosive Breaching in U.S. Military Warfighters.

Authors:  Zhaoyu Wang; Caroline M Wilson; Yongchao Ge; Jeffrey Nemes; Christina LaValle; Angela Boutté; Walter Carr; Gary Kamimori; Fatemeh Haghighi
Journal:  Front Neurol       Date:  2020-10-23       Impact factor: 4.003

  10 in total

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