A Study on the Genetic Inheritance of Ankyloglossia Based on Pedigree Analysis

被引:10
作者
Han, Soo-Hyung [1 ]
Kim, Min-Cheol [1 ]
Choi, Yun-Seok [2 ]
Lim, Jin-Soo [1 ]
Han, Ki-Taik [1 ]
机构
[1] St Vincents Hosp, Dept Plast & Reconstruct Surg, Suwon, South Korea
[2] Catholic Univ Korea, St Pauls Hosp, Sch Med, Dept Plast & Reconstruct Surg, Seoul 442723, South Korea
来源
ARCHIVES OF PLASTIC SURGERY-APS | 2012年 / 39卷 / 04期
关键词
Lingual frenum; Pedigree; X-chromosome;
D O I
10.5999/aps.2012.39.4.329
中图分类号
R61 [外科手术学];
学科分类号
摘要
Background Ankyloglossia or tongue-tie is a congenital anomaly characterized by an abnormally short lingual frenum. Its prevalence in the newborn population is approximately 4%. Its mode of inheritance has been studied in some articles, but no conclusion has been established. Also, no relevant report has been published in Korea. This study was conducted to elucidate the genetic inheritance of ankyloglossia via pedigree analysis. Methods In this study, 149 patients with no other congenital anomaly who underwent frenuloplasty between March 2001 and March 2010 were studied. Pedigrees were made via pre-or post-operative history taking, and patients with uncertain histories were excluded. In the patient group that showed a hereditary nature, the male-to-female ratio, inheritance rate, and pattern of inheritance were investigated. Results One hundred (67.11%) of the patients were male and 49 (32.89%) were female (male-female ratio= 2.04: 1). Ninety-one (61.07%) patients reported no other relative with ankyloglossia, and 58 (38.93%) patients had a relative with this disease. The inheritance rate was 20.69% in the 58 cases with a hereditary nature. In the group with no family history of ankyloglossia, the male-female ratio was 3.79: 1, which significantly differed from that of the group with a family history of ankyloglossia. X-chromosome mediated inheritance and variation in the gene expression was revealed in the pedigree drawn for the groups with hereditary ankyloglossia. Conclusions Ankyloglossia has a significant hereditary nature. Our data suggest X-linked inheritance. This study with 149 patients, the first in Korea, showed X-linked inheritance in patients with a sole anomaly.
引用
收藏
页码:329 / 332
页数:4
相关论文
共 13 条
[1]   Ankyloglossia: Assessment, incidence, and effect of frenuloplasty on the breastfeeding dyad [J].
Ballard, JL ;
Auer, CE ;
Khoury, JC .
PEDIATRICS, 2002, 110 (05) :e63
[2]   Effect of α-globin genotype on the pathophysiology of sickle cell disease [J].
Ballas, SK .
PEDIATRIC PATHOLOGY & MOLECULAR MEDICINE, 2001, 20 (02) :107-121
[3]   The T-box transcription factor gene TBX22 is mutated in X-linked cleft palate and ankyloglossia [J].
Braybrook, C ;
Doudney, K ;
Marçano, ACB ;
Arnason, A ;
Bjornsson, A ;
Patton, MA ;
Goodfellow, PJ ;
Moore, GE ;
Stanier, P .
NATURE GENETICS, 2001, 29 (02) :179-183
[4]  
HARRIS EF, 1992, CLEFT PALATE-CRAN J, V29, P72, DOI 10.1597/1545-1569(1992)029<0072:EPOAWM>2.3.CO
[5]  
2
[6]   Inheritance of ankyloglossia (tongue-tie) [J].
Klockars, T. ;
Pitkaranta, A. .
CLINICAL GENETICS, 2009, 75 (01) :98-99
[7]   Familial ankyloglossia (tongue-tie) [J].
Klockars, Tuomas .
INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY, 2007, 71 (08) :1321-1324
[8]   TBX22 mutations are a frequent cause of cleft palate [J].
Marçano, ACB ;
Doudney, K ;
Braybrook, C ;
Squires, R ;
Patton, MA ;
Lees, MM ;
Richieri-Costa, A ;
Lidral, AC ;
Murray, JC ;
Moore, GE ;
Stanier, P .
JOURNAL OF MEDICAL GENETICS, 2004, 41 (01) :68-74
[9]  
Marcus D M, 1989, Immunol Ser, V43, P685
[10]   Ankyloglossia - Incidence and associated feeding difficulties [J].
Messner, AH ;
Lalakea, ML ;
Aby, J ;
Macmahon, J ;
Bair, E .
ARCHIVES OF OTOLARYNGOLOGY-HEAD & NECK SURGERY, 2000, 126 (01) :36-39